biology

Neurobiology of Disease

Neuronal Mitochondria Modulation of LPS-Induced Neuroinflammation

Micah Harland,1 Sandy Torres,1 Jingyi Liu,1 and Xinglong Wang1,2 1Department of Pathology, and 2Center for Mitochondrial Diseases, Case Western Reserve University, Cleveland, Ohio 44106

Neuronal mitochondria dysfunction and neuroinflammation are two prominent pathological features increasingly realized as important pathogenic mechanisms for neurodegenerative diseases. However, little attempt has been taken to investigate the likely interactions between them. Mitofusin2 (Mfn2) is a mitochondrial outer membrane protein regulating mitochondrial fusion, a dynamic process essential for mitochondrial function. To explore the significance of neuronal mitochondria in the regulation of neuroinflammation, male and female transgenic mice with forced overexpression of Mfn2 specifically in neurons were intraperitoneally injected with lipopolysac- charide (LPS), a widely used approach to model neurodegeneration-associated neuroinflammation. Remarkably, LPS-induced lethality was almost completely abrogated in neuronal Mfn2 overexpression mice. Compared with nontransgenic wild-type mice, mice with neuronal Mfn2 overexpression also exhibited alleviated bodyweight loss, behavioral sickness, and myocardial dysfunction. LPS-induced release of IL-1� but not TNF-� was further found greatly inhibited in the CNS of mice with neuronal Mfn2 overexpression, whereas peripheral inflammatory responses in the blood, heart, lung, and spleen remained unchanged. At the cellular and molecular levels, neuronal Mfn2 suppressed the activation of microglia, prevented LPS-induced mitochondrial fragmentation in neurons, and importantly, upregulated the expression of CX3CL1, a unique chemokine constitutively produced by neurons to suppress microglial activation. Together, these results reveal an unrecognized possible role of neuronal mitochondria in the regulation of microglial activation, and propose neuronal Mfn2 as a likely mechanistic linker between neuronal mitochondria dysfunction and neuroinflammation in neurodegeneration.

Key words: LPS; Mfn2; mitochondrial dynamics; neuroinflammation; sepsis; septic myocardial dysfunction

Introduction Progressive loss or dysfunction of neurons in the CNS or periph- eral nervous system (PNS) is a characteristic feature of a wide range of neurodegenerative disorders including Alzheimer’s disease (AD), Parkinson’s disease, Huntington’s disease, amyo- trophic lateral sclerosis (ALS), and frontotemporal lobar degen- eration. Although the cause that drives the progression of each of these neurodegenerative diseases remains elusive, it has been well recognized that these devastating diseases are multifactorial and

involve many pathogenic mechanisms such as glutamate excito- toxicity, oxidative stress, neuroinflammation, and mitochondrial dysfunction in addition to the widely studied accumulation of misfolded or aggregated proteins. Among them, mitochondrial dysfunction and neuroinflammation have been extensively stud- ied in the past decade. As prominent pathological features, both mitochondrial dysfunction and neuroinflammation are closely associated with pathological hallmarks (Heneka et al., 2015; Gao et al., 2017), and have been implicated as interdependent pathological lesions in neurodegenerative diseases (Wilkins and Swerdlow, 2016). However, despite intensive effort devoted to understanding the un- derlying cause(s) of these two prominent pathological features for neurodegenerative diseases, a clear mechanistic linker(s) between them has yet to be identified.

Mitofusin2 (Mfn2) is a conserved dynamin-like GTPase pro- tein predominantly localized in the mitochondrial outer mem- brane regulating mitochondrial fusion (Chen et al., 2003), a process reported to be essential for various aspects of mitochon-

Received Sept. 27, 2019; revised Dec. 4, 2019; accepted Jan. 1, 2020. Author contributions: X.W. designed research; M.H., S.T., and J.L. performed research; M.H. and X.W. wrote the

paper. This work was supported by Grants from the US NIH (1R01NS097679 and RF1AG056320) and U.S. Alzheimer’s

Association (AARG-17-499682). The authors declare no competing financial interests. Correspondence should be addressed to Xinglong Wang at [email protected]. https://doi.org/10.1523/JNEUROSCI.2324-19.2020

Copyright © 2020 the authors

Significance Statement

Our study suggests that Mfn2 in neurons contributes to the regulation of neuroinflammation. Based on the remarkable suppres- sion of LPS-induced neuroinflammation and neurodegeneration-associated mitochondrial dysfunction and dynamic abnormal- ities by neuronal Mfn2, this study centered on Mfn2-mediated neuroinflammation reveals novel molecular mechanisms that are involved in both mitochondrial dysfunction and neuroinflammation in neurodegenerative diseases. The pharmacological target- ing of Mfn2 may present a novel treatment for neuroinflammation-associated diseases.

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drial function including respiratory complex assembly (Cogliati et al., 2013), ATP production (Benard et al., 2007), Ca 2� homeo- stasis (Frieden et al., 2004; Szabadkai et al., 2004), and reactive oxygen species production (Yu et al., 2006). Mfn2 has also been reported to be present in the endoplasmic reticulum (ER) or mitochondria-associated membranes to regulate ER and mito- chondria tethering (de Brito and Scorrano, 2008; Sebastián et al., 2012; Sugiura et al., 2013), autophagosome formation (Hailey et al., 2010), autophagosome-lysosome fusion (Zhao et al., 2012), mitophagy (McLelland et al., 2018), and axonal transport of cal- pastatin, an endogenous specific inhibitor of the calpain sys- tem, to maintain neuromuscular synapses based on our most recent study (Wang et al., 2018). Altered mitochondrial dy- namics (Kandimalla et al., 2016), distribution (Kopeikina et al., 2011), function (David et al., 2005), transport (Rodríguez- Martín et al., 2016), ER/mitochondria association (Perreault et al., 2009), autophagy (Schaeffer et al., 2012), and calpain (Reinecke et al., 2011), all Mfn2-related pathways, have been con- sistently observed in experimental models for neurodegenerative diseases.

Sepsis is a multi-symptomatic, life-threatening immune reaction to an infection. Although sepsis and neurodegenerative diseases are generally thought to be unrelated, both share similar neuroinflam- mation and neurologic symptoms (Sankowski et al., 2015). Additionally, a growing body of evidence supports that neuroin- flammation and neurodegeneration can be initiated by robust in- flammatory events in the periphery, including single dose lipopolysaccharide (LPS; Sheng et al., 2003; Kitazawa et al., 2005; Qin et al., 2007; Sy et al., 2011; Ifuku et al., 2012; Okuyama et al., 2013; Jin et al., 2014). Despite previous studies reporting altered mitochondrial dynamics in heart, lung, liver, kidney, and skeletal muscle tissue in sepsis animal models (Hansen et al., 2015; Liu et al., 2015; Yu et al., 2016; Park et al., 2018; Haileselassie et al., 2019; Tan et al., 2019), their role in the CNS during sepsis remains largely un- known. To examine this, we generated transgenic mice overexpress- ing Mfn2 specifically in CNS neurons under the control of Thy1.2 promotor, i.e., TMFN mice (Wang et al., 2015, 2018) and investi- gated the role of neuronal Mfn2 in neuroinflammation by intraperi- toneally injecting TMFN and age-matched nontransgenic (NTg) mice with LPS, one of the most widely used approaches for periph- erally induced neuroinflammation (Catorce and Gevorkian, 2016), and explored the potential pathways by which neuronal mitochon- dria regulate neuroinflammation via Mfn2.

Materials and Methods Transgenic mice. All mouse procedures were performed in accordance

with NIH guidelines and the Institutional Animal Care and Use Com- mittee (IACUC) at Case Western Reserve University (CWRU). Mfn2 transgenic (TMFN) mice were created via pronuclear injection of the murine Thy1.2 genomic expression cassette (gift from Dr. Philip C. Wong, Johns Hopkins University) expressing human Mfn2 into C57BL/6 fertilized eggs. C57BL/6 Mfn2fl/fl mice were obtained from Dr. David Chan (California Institute of Technology). All experiments used 3-month- old male and female littermates raised in specific pathogen-free facilities. The animal number needed to reach statistical significance was calcu- lated and reviewed by CWRU IACUC before the experiments.

LPS injection and survival. Three-month-old littermate mice were intra- peritoneally injected with 10 mg/kg bodyweight of 0.22 �m Millex filtered O111:B4 LPS (L2630, Sigma Aldrich) in PBS (in mM: 137 NaCl, 2.7 KCl, 10 Na2HPO4, 17.6 KH2PO4, pH 7.4) or an equal volume of PBS ipsilaterally. Sur- vival was assessed daily up to 14 d postinjection (dpi), at which point remaining mice were killed in accordance with CWRU IACUC protocol.

Intrahippocampal injection. Three-month-old mice were intrahip- pocampally injected with 1 �l of AAV1-shCX3CL1 and AAV1-

Scrambled control (TMFN and NTg mice) or AAV1-Cre-EGFP and AAV1-EGFP control (Mfn2fl/fl mice; all from Vector Biolabs) on the left and right sides of the mice, respectively. Briefly, mice were anesthetized with 2% isoflurane inhalation and maintained at 2% via nosecone. A stereotactic platform with heating pad support was used to position the heads of the mice. Eye ointment was administered and the necks/heads of the mice were shaved before sterilization with betadine/alcohol. Bupiva- caine/lidocaine (1:1 v/v) was injected subcutaneously at the base of the neck. The skull was exposed with a scalpel midline incision from the frontal cranial bones to the parietal cranial bones. Small holes were drilled in the skull and AAV1 was injected (2.1 mm anteroposterior, �2.0 mm mediolateral, and �1.5 mm dorsoventral relative to bregma) with a 30-gauge needle at a rate of 0.2 �l/min followed by 5 additional minutes for absorption. The incision was closed with nylon suture, carprofen was intraperitoneally administered, and mice were returned to a clean cage with warming pad for recovery. At 15 dpi, TMFN and NTg mice were intraperitoneally injected with 10 mg/kg LPS and killed 2 d later (17 dpi of AAV1). Mfn2fl/fl mice were killed at 21 dpi.

Microglia depletion. Three-month-old TMFN and NTg littermate mice were fed Purina Prolab RMH 3000 chow (5P75, Lab Diets) with or with- out 290 mg/kg PLX3397 (206178, MedKoo Biosciences) prepared by Lab Diets ad libitum for 4 weeks. Mice were intraperitoneally injected with 10 mg/kg LPS or PBS control and remained on PLX3397 or control diet during the experiments.

Open-field tests. Open-field tests were conducted at 2 dpi during sim- ilar daytimes. A multiple unit open-field maze consisting of four cham- bers (50 cm length � 50 cm width � 38 cm height) was used for all tests. Each chamber was wiped with 10% ethanol before use and before subse- quent tests to remove scent cues left by the previous mouse. Four lamps were placed at the outside corners of the test unit to allow for ample visibility within the chambers. Mice were acclimated in the chamber for 3 min before each trial and video recorded for 10 min. Anymaze 6.13 software (Stoelting) was used to evaluate mouse movement/position (immobility settings at 65% and 2 s). Inner zones were defined as a 40 cm length � 40 cm width square in the center of each chamber. Total trav- eled distance, immobile time, average speed, body rotations, and track plots were calculated using Anymaze 6.13.

Tissue collection. The majority of tissues and whole blood were col- lected at 2 dpi unless specified otherwise in the text. Briefly, mice were anesthetized with 2% isoflurane inhalation and killed via cervical dislo- cation for collection of non-perfused tissues. Perfused tissues, used where specified, were collected from mice anesthetized with Avertin (tri- bromoethanol, 2.5% in PBS) and transcardially perfused with 4°C PBS for 6 min. Tissues for lysates were snap frozen on dry ice and stored at �80°C before processing. Tissues for embedding were fixed in 10% for- malin, dehydrated in increasing ethanol concentrations (70, 95, and 100%), cleared in 100% xylene, and paraffinized in blocks.

Electrocardiogram. Electrocardiogram (ECG) recordings of mouse cardiac function was performed using the PowerLab 4/35 data acquisi- tion system, FE136 Animal Bio Amp, and 29-G needle electrodes (AD- Instruments). Mice were anesthetized with 2% isoflurane inhalation and maintained at 2% via nosecone. Sterile electrodes were inserted �1 cm subcutaneously proximal to each side of the thorax near the upper limbs and a reference grounding electrode was inserted subcutaneously near the left lower limb. ECGs were recorded with LabChart 8.1.13 software (ADInstru- ments) for 5 min with a 4000/s sampling rate. A low-pass filter with a cutoff frequency of 50 Hz was applied to improve signal-to-noise ratio. ECGs were block averaged to produce a single representative ECG and LabChart 8.1.13 software was used to automatically identify wave positions and amplitudes. Parameters were qualitatively validated against published mouse ECGs (Ho et al., 2011; Boukens et al., 2014) to ensure proper denotation of waves. Amplitude was measured as the voltage difference between 0 mV baseline to the peak of each wave. Time intervals were measured as the time difference from the peak of one wave to another.

Hematology. Mouse tail-vein blood samples were collected in Mi- crovette 200 lithium heparin capillary tubes (Sarsedt). White blood cell differentials were assessed with HEMAVET 950 hematology system (Drew Scientific). Plasma was prepared by centrifugation (1000 � g, 4°C) of tail vein blood for 10 min followed by collection of the clear top layer.

Harland et al. • Mitochondria for Neuroinflammation J. Neurosci., February 19, 2020 • 40(8):1756 –1765 • 1757

Immunoblotting. Mouse tissues were lysed in 1� lysis buffer (9801, Cell Signaling Technology) with 1 mM phenylmethyl sulfonyl fluoride (10837091001, MilliporeSigma), Protease Inhibitor Cocktail (P8340, MilliporeSigma), and Phosphatase Inhibitor (4906845001, Roche). Pro- tein concentrations were resolved using Pierce BCA Protein Assay (23227, ThermoFisher Scientific). Equal protein concentrations and vol- umes were run on 10% SDS-PAGE gels and blotted on Immobilon-P (IPVH00010, MilliporeSigma). Blots were blocked in 10% nonfat milk in tris-buffered saline Tween (TBST; 50 mM Tris and 150 mM NaCl, 0.1% Tween20, pH 7.6) before probing with primary and detection anti- bodies in 1% milk in TBST. Blots were developed with Immobilon Western chemiluminescent horse radish peroxidase (HRP) substrate (WBKLS0500, MilliporeSigma) or ImmunoCruz Western Blotting Luminol Reagent (sc-2048, Santa Cruz Biotechnology) and imaged with ChemiDoc MP Imaging System (Bio-Rad).

Primary antibodies (all diluted 1:3000 in TBST from stock concentra- tions): mouse monoclonal anti-Drp1 (611112, BD Biosciences), rabbit monoclonal anti-GAPDH (2118, Cell Signaling Technology), mouse monoclonal anti- glial fibrillary acidic protein (GFAP; 14-9892-82, In- vitrogen), mouse monoclonal anti-HIF-1� (610958, BD Biosciences), rabbit monoclonal anti-Iba1 (013-27691, Wako Chemical), rabbit poly- clonal anti-MFF (12741, Abcam), mouse monoclonal anti-Mfn1 (sc- 166644, Santa Cruz Biotechnology), mouse monoclonal anti-Mfn2 (sc-100560, Santa Cruz Biotechnology), rabbit monoclonal anti-Mfn2 (11925, Cell Signaling Technology), mouse monoclonal anti-Opa1 (612606, BD Biosciences), rabbit polyclonal anti-MAP2 (AB5622, Milli- poreSigma), rabbit monoclonal anti-Synaptophysin (5461S, Cell Signal- ing Technology), and mouse monoclonal anti- voltage-dependent anion channel 1 (VDAC1; ab14734, Abcam). Detection antibodies (diluted 1:10,000 in TBST from stock concentrations): anti-rabbit IgG, HRP- linked (7074S, Cell Signaling Technology), and anti-mouse IgG, HRP- linked (7076S, Cell Signaling Technology).

Immunohistochemistry (IHC). Formaldehyde-fixed paraffin embedded mouse tissue was used to prepare serial adjacent sections. Tissue sections were de-paraffinized with 100% xylene twice and rehydrated with de- creasing ethanol concentrations (100, 95, 70, and 50%) before incuba- tion in tris-buffered saline (TBS; 50 mM Tris and 150 mM NaCl, pH 7.6). Tissue antigen retrieval was conducted with 1� immunoDNA retriever with citrate (BSB 0021, Bio SB) in a TintoRetriever pressure cooker (BSB 7008, Bio SB). Slides were rinsed with deionized (DI) water and incu- bated with TBS. Individual sections were circled with hydrophobic marker and blocked with 10% normal goat serum (NGS; 50062Z, Ther- moFisher Scientific) in TBS for 30 min at room temperature. Sections were rinsed with 1% NGS in TBS and excess liquid was removed with a paper towel. Sections were incubated with primary antibodies diluted in 1% NGS in TBS overnight at 4°C, then rinsed and incubated with 1% followed by 10% NGS in TBS. Species-specific secondary antibodies were then placed on the tissue sections for 30 min at room temperature. Sec- tions were rinsed and incubated in 1 and 10% NGS an additional time before incubation with species-specific peroxidase-anti-peroxidase for 1 h at room temperature. Slides were developed using a DAB chromogen kit (DB801L, Biocare Medical; or ENZ-ACC105, Enzo Life Sciences). Tris buffer (50 mM Tris, pH 7.6) was used to stop the reaction and slides were rinsed with DI water and dehydrated with 70, 95, 100% ethanol, and xylene. Coverslips were mounted with Permount (SP15-500, Fisher Sci- entific). Slides were imaged using a Zeiss Axio Imager.A2 equipped with an AxioCam 503 using Zeiss EC Plan-Neofluar 10� and 20� objectives.

For hematoxylin and eosin staining, tissue sections were rehydrated in decreasing ethanol concentrations as above and then placed in DI water. Slides were incubated in hematoxylin for 3 min, rinsed in DI water, and excess stain removed with acid alcohol. Slides were thoroughly rinsed with DI water and incubated in eosin for 30 s. Sections were dehydrated in 95 and 100% ethanol followed by xylene. Coverslips were mounted and slides were imaged as described for immunohistochemistry.

Primary antibodies (diluted in 1% NGS in TBS from stock concentra- tions): mouse monoclonal anti-GFAP (1:250; 14-9892-82, Invitrogen), rab- bit monoclonal anti-Iba1 (1:250; 013-27691, Wako Chemical), rabbit monoclonal anti-Ki-67 (1:100; 9129S, Cell Signaling Technology), rabbit polyclonal anti-MAP2 (1:500; AB5622, MilliporeSigma), mouse mono-

clonal anti-NeuN (1:1000; MAB377, MilliporeSigma), rabbit monoclo- nal anti-synaptophysin (1:100; 5461S, Cell Signaling Technology). Secondary and detection antibodies: goat anti-mouse IgG (1:50; AP124, MilliporeSigma), goat ant-rabbit IgG (1:50; AP132, MilliporeSigma), mouse peroxidase-anti-peroxidase (1:250; 223-005-024, Jackson Immu- noResearch), rabbit peroxidase-anti-peroxidase (1:250; 323-005-024, Jackson ImmunoResearch).

Immunofluorescent microscopy. Formaldehyde-fixed paraffin embed- ded mouse tissue was sectioned, de-paraffinized, rehydrated, and antigen retrieved. Slides were rinsed with DI water and incubated with PBS. Sections were circled with a hydrophobic marker and blocked with 10% NGS in PBS for 30 min. Sections were rinsed with 1% NGS in PBS and incubated with individual primary antibodies at 4°C overnight. Sections were then rinsed with 1% NGS, blocked in 10% NGS for 10 min, and rinsed with 1% NGS. Sections were incubated with species-specific Alex- aFluor 488- or 568-conjugated Abs diluted 1:300 in PBS for 2 h at room temperature in the dark. Sections were rinsed 3� with PBS, incubated with DAPI diluted 1:1000 in PBS for 15 min, and rinsed 3� with PBS. Excess liquid was removed and slides were coverslipped using Fluoromount-G mounting medium (0100-01, SouthernBiotech). Slides were imaged using a Zeiss Celldiscoverer 7 equipped with an AxioCam 512 and Hamamatsu Orca Flash 4.0 V3 using Zeiss Plan-Apochromat 20� and 50� autocorr objectives with 0.5�, 1�, and 2� magnification changers.

Primary antibodies (diluted in 1% NGS in PBS from stock concentra- tions): rabbit monoclonal anti-Iba1 (1:250; 013-27691, Wako Chemical), mouse monoclonal anti-VDAC1 (1:3000; ab14734, Abcam). Detection an- tibodies: anti-mouse IgG (H�L) AlexaFluor 568 (1:300; A-11031, Invitro- gen), anti-rabbit IgG (H�L) AlexaFluor 488 (1:300; A-11034, Invitrogen).

Enzyme-linked immunosorbent assay (ELISA). Optical 96-well plates were coated with polyclonal antigen capture antibody in ELISA Coating Buffer (421701, BioLegend) or, for CX3CL1 direct ELISA, 20 �g/ml mouse brain extract in PBS overnight at 4°C. Wells were aspirated and blocked with 1% bovine serum albumin (BSA) in PBS for 1.5 h at room temperature. Wells were aspirated, rinsed 3� with PBS, and aspirated. Recombinant protein standards and samples diluted in PBS were incu- bated in individual wells overnight at 4°C. Wells were aspirated, rinsed with PBS 3�, and aspirated. Primary antibody targeting the antigen of interest was diluted in PBS and added to each well. The plate was incu- bated at 4°C overnight. After aspirating, rinsing 3�, and aspirating again, each well was incubated in diluted species-specific HRP-conjugate detec- tion antibody for 2 h at room temperature. Wells were aspirated, rinsed 4�, aspirated, and then developed with TMB substrate (N301, Thermo- Fisher Scientific) at 37°C for 30 min. 450 nm stop solution (ab171529, Abcam) was added each well. The OD450 of each well was read with a BioTek 800TS microplate reader. Standard curves and protein concen- trations were calculated from triplicate well averages in Microsoft Excel.

Capture antibodies (diluted in PBS): rabbit polyclonal anti-IL-1� (1 �g/ml; ab9722, Abcam), rabbit polyclonal anti-TNF� (0.5 �g/ml; ab6671, Abcam). Primary antibodies: rabbit polyclonal anti-CX3CL1 (1 �g/ml; PA1–29026, Invitrogen), mouse monoclonal anti-IL-1� (1 �g/ml; MAA563Mu21, Cloud-Clone), mouse monoclonal anti- TNF� (1 �g/ml; MAA133Mu21, Cloud-Clone). Detection antibodies (diluted 1:1000 in 1% BSA in PBS from stock concentrations): anti- rabbit IgG, HRP-linked (7074S, Cell Signaling Technology), anti-mouse IgG, HRP-linked (7076S, Cell Signaling Technology). Protein standards: recombinant mouse IL-1� (ab78839, Abcam), recombinant mouse TNF� (ab9740, Abcam).

Real-time PCR. Total RNA was isolated from fresh perfused mouse whole brain tissue using RNeasy Mini kit (74104, Qiagen) according to the manufacturer’s specifications. Complimentary DNA was synthesized using High-Capacity cDNA Reverse Transcription kit (4368814, Applied Biosystems) and Simpliamp Thermal Cycler (ThermoFisher Scientific) according to the manufacturer’s cycling parameters. Real-time PCR for target mRNAs was assayed using Power SYBR Green Master Mix (4367660, Applied Biosystems) in a StepOne Real-Time PCR System (Life Technologies) according to the manufacturer’s cycling parameters. StepOne 2.3 software (Life Technologies) was used to measure CT values

1758 • J. Neurosci., February 19, 2020 • 40(8):1756 –1765 Harland et al. • Mitochondria for Neuroinflammation

and fold-change standardized to GAPDH mRNA was calculated in Microsoft Excel.

The following primer pairs were used: CX3CL1 F: 5�-CGCGTTCTTC CATTTGTGTA-3� and R: 5�-CTGTGTCGTCTCCAGGACAA-3�, CX3 CR1 F: 5�-CAGCATCGACCGGTACCTT-3� and R: 5�-GCTGCACT GTCCGGTTGTT-3�, GAPDH F: 5�-ATGTTCCAGTATGACTCCAC TCACGG-3� and R: 5�-GAAGACACCAGTAGACTCCACGACA-3�, IL-1� F: 5�-AACCTGCTGGTGTGTGACGTTC-3� and R: 5�-CAGCAC GAGGCTTTTTTGTT GT-3�, IL-6 F: 5�-ACAACCACGGCCTTCCCT ACTT-3� and R: 5�-CACGATTTCCCAGAGAACATGTG-3�, IL-10 F: 5�-ATAACTGCACCCACTTCCCA-3� and R: 5�-GGGCATCACTTC TACCA GGT-3�, TNF� F: 5�-CTCCAGGCGGTGCCTATGT-3� and R: 5�-GAAGAGCGTGGTGGCCC-3�.

Image analysis. Immunoblot band densities were quantified with open-source WCIF ImageJ (developed by W. Rasband at the National Institutes of Health) and Image Lab 6.0.1 (Bio-Rad). IHC staining and immunofluorescent intensities were quantified with ZEN 2.3 (Carl Zeiss Microscopy). Immunofluorescent VDAC1 (AF568; green) and DAPI (blue) Z-stacks were processed for background subtraction and con- strained iterative deconvolution before 3D projection in Zen software. Wide-field VDAC1 Z-stack images were similarly processed and mito- chondrial length were calculated from single plane images using Zen 2.3 automated image analysis and Microsoft Excel. Mitochondrial length was defined as the Feret maximum ( F).

Experimental design and statistical analysis. Statistical analyses were conducted with Prism 8.0 (GraphPad). Data are mean � SEM. Data were compared by unpaired two-tailed t tests for two samples or one-way ANOVA followed by Tukey’s multiple comparison post hoc test for �3 samples. Sample size (n) was defined as the number of cells counted in imaging experiments, or the number of mice per experimental group. The null hypothesis was rejected at the 0.05 level. p values 0.05 were considered statistically significant. The statistical test, sample size (n), and the p values are all described in the figure legends.

Results TMFN mice are resistant to LPS-induced endotoxic shock Mfn2 was only upregulated in the brain and spinal cord of TMFN mice and no transgene expression was noted in the peripheral immune system and other tis- sues, including the heart, lung, gastro- cnemius muscle, liver and kidney (Fig. 1-1 A, B, available at https://doi.org/10. 1523/JNEUROSCI.2324-19.2020.f1-1). Three-month-old TMFN and NTg litter- mates were intraperitoneally injected with a single lethal dose of LPS or PBS. Survival was monitored for up to 14 d, whereas all other assays were conducted at 2 dpi (Fig. 1A). After intraperitoneal injection of le- thal dose LPS, 3-month-old NTg mice showed body weight loss and died largely within 1 week (Fig. 1B and Fig. 1-1C, available at https://doi.org/10.1523/ JNEUROSCI.2324-19.2020.f1-1). In striking contrast, TMFN mice demonstrated signifi- cantly alleviated body weight loss and most survived after lethal dose LPS challenge (Fig. 1-1C, available at https://doi.org/10.1523/ JNEUROSCI.2324-19.2020.f1-1), even though they also exhibited symptoms of acute illness. LPS-induced splenomegaly, a prominent feature reported in experi- mental sepsis models (Altamura et al., 2001), was similar in NTg and TMFN lit-

termates (Fig. 1-1 D, available at https://doi.org/10.1523/ JNEUROSCI.2324-19.2020.f1-1). Weights of other tissues or organs were also identical, and showed similar pathological dam- age between NTg and TMFN littermates (Fig. 1-1 D, E, available at https://doi.org/10.1523/JNEUROSCI.2324-19.2020.f1-1), suggesting that peripheral inflammatory responses and gross or- gan constitution are likely analogous in TMFN and NTg mice with LPS injection. Three independent lines of TMFN mice with similar transgene expression were tested and there was no phe- notypic difference between them. Nonspecific psychological and behavioral symptoms, usually referred to as “sickness behavior”, virtually accompany all acute inflammatory illnesses (Dantzer et al., 2008). To further investigate whether LPS-induced sickness be- havior was improved in TMFN mice, we assessed the performance of mice in the open field test at 2 dpi. Compared with mice with PBS injection, NTg mice with LPS injection showed greatly reduced trav- eling distance and stayed largely immobile in proximity to the walls of the maze (Fig. 1C,D), indicative of both locomotor impairment and anxiety-related behavior. TMFN mice with LPS injection exhib- ited greater overall movement throughout the test with augmented distance traveled, reduced time spent immobile, and less wall- hugging behavior (Fig. 1C,D). Together, these data demonstrate that forced expression of Mfn2 in neurons is sufficient to greatly alleviate LPS-induced endotoxic shock and associated behavioral sickness.

LPS-induced neuroinflammation is attenuated in TMFN mice Peripheral LPS challenge causes widespread immune activation, including lasting neuroinflammation and neuronal dysfunction in mice (Catorce and Gevorkian, 2016). However, TMFN and NTg mice with the same injection type showed no differences in leukopenia and levels of plasma proinflammatory cytokines

Figure 1. Forced Mfn2 expression in neurons attenuates LPS-induced mortality and behavioral sickness. A, Experimental design for the intraperitoneal LPS injection experiment. Three-month-old TMFN and NTg littermates were intraperitoneally injected with a single dose of LPS (10 mg/kg bodyweight) or PBS and survival was assessed up to 14 dpi, whereas all other assays were conducted at 2 dpi. B, Kaplan–Meier survival curve of TMFN and NTg mice following LPS injection (n 10 mice/group). C, D, Representative track plots (C) and quantifications (D) of average distance traveled, immobility duration, average speed, and body rotations of TMFN and NTg mice at 2 dpi in open-field tests (n 10 mice/group). Error bars represent mean � SEM, representative of triplicate experiments. Student’s t test or one-way ANOVA followed by Tukey’s multiple-comparison test. **p 0.01, ***p 0.001, ****p 0.0001. ns, Nonsignificant. For further details on Mfn2 expression and pathology in TMFN mice see Figure 1-1, available at https://doi.org/10.1523/JNEUROSCI.2324-19.2020.f1-1. For cardiac dysfunction see Figure 1-2, available at https://doi. org/10.1523/JNEUROSCI.2324-19.2020.f1-2.

Harland et al. • Mitochondria for Neuroinflammation J. Neurosci., February 19, 2020 • 40(8):1756 –1765 • 1759

IL-1� and TNF� (Fig. 2-1 A–C, available at https://doi.org/ 10.1523/JNEUROSCI.2324-19.2020.f2-1), further supporting that peripheral inflammation is unaltered in TMFN mice. Since plasma is specific to the circulatory system and does not consti- tute the entire immune environment, we then examined IL-1� and TNF� in multiple tissues from TMFN and NTg mice at 2 dpi, including the brain, spinal cord, heart, lung, and spleen. Consis- tent with their elevated plasma levels, both IL-1� and TNF� were greatly increased in these tissues of TMFN and NTg mice with LPS challenge (Fig. 2 A, B). Surprisingly, although TNF� was sim- ilarly high in all surveyed tissues of LPS-treated TMFN and NTg mice, LPS-induced IL-1� increase was remarkably suppressed specifically in the brain and spinal cord of TMFN mice (Fig. 2 A, B, and Fig. 2-1 D, available at https://doi.org/10.1523/ JNEUROSCI.2324-19.2020.f2-1). Subsequent gene expression analyses validated the specific inhibition of IL-1� but not IL-6, IL-10, or TNF� at the mRNA level in the brains of TMFN mice with LPS injection compared with NTg mice with LPS (Fig. 2C). Of note, these cytokines were similar at basal levels in TMFN and NTg mice (Fig. 2A–C). These results indicate that forced Mfn2 expression in neurons attenuates peripherally induced neuroin- flammation, likely through specific diminished induction of pro- inflammatory IL-1�.

LPS-induced microglia activation is suppressed in TMFN mice IL-1� is the main inflammatory mediator of the CNS and, when augmented, is commonly accompanied by microglia activation (Liu and Quan, 2018). Because TMFN mice displayed reduced IL-1� in the CNS following LPS injection, we next sought to determine whether microglia were differentially activated in TMFN mice. Brain sections from TMFN and NTg mice at 2 dpi were stained for ionized calcium binding adaptor molecule 1 (Iba1), a well established marker of microglia activation (Hoogland et al., 2015). Microglia of NTg mice with LPS injec- tion exhibited fewer processes and increased Iba1 staining, indi- cating microglia activation in the brain (Fig. 3 A, B). In contrast,

TMFN microglia maintained ramified, inactive morphology with weak Iba1 staining after peripheral LPS challenge (Fig. 3 A, B). Staining for GFAP, a marker of astrocyte activation, was in- creased to similar levels in the brains and spinal cords of TMFN and NTg mice with LPS injection (Fig. 3-1 A, B, available at https://doi.org/10.1523/JNEUROSCI.2324-19.2020.f3-1). To further quantify whether microglia were inactive in TMFN mice following LPS injection, we conducted immunofluorescent staining for Iba1 in the brains of TMFN and NTg mice at 2 dpi. Microglia in NTg mice with LPS had rounded morphology with fewer processes that were shorter on average (Fig. 3C,D, and Fig. 3-1C, available at https://doi.org/10.1523/JNEUROSCI.2324- 19.2020.f3-1). Contrastingly, microglia morphology, process number, and Iba1 intensity were unaltered by LPS injection in TMFN mice with average process length only decreasing slightly compared with PBS injected control mice (Fig. 3C,D). To con- firm that microglia were explicitly inactive in TMFN mice, we immunoblotted for Iba1 and GFAP in brain extracts from TMFN and NTg mice at 2 dpi. Iba1 levels were greatly increased in NTg mice with LPS injection, but only marginally increased in TMFN mice with LPS (Fig. 3-1 D, available at https://doi.org/10.1523/ JNEUROSCI.2324-19.2020.f3-1). GFAP was increased equally in brains of TMFN and NTg mice with LPS injection (Fig. 3-1 D, available at https://doi.org/10.1523/JNEUROSCI.2324-19.2020.f3-1), suggesting that microglia quiescence is likely driving reduced neuroin- flammation in TMFN mouse brains.

LPS-induced mitochondrial fragmentation in neurons is inhibited in TMFN mice To determine whether LPS could induce mitochondrial fragmen- tation in neurons of mice and whether forced Mfn2 expression could prevent this, mitochondrial morphology was assessed by immunofluorescent staining for mitochondria marker VDAC1 in brain sections from TMFN and NTg mice at 2 dpi. Compared with neurons of NTg mice, mitochondria in TMFN mouse neurons became elongated as evidenced by the increase in mitochondrial length; Fig. 4 A, B, and Fig. 4-1 A, B, available at

Figure 2. TMFN mice are protected from peripheral LPS-induced neuroinflammation. IL-1� (A) and TNF� (B) concentrations in the indicated tissues of TMFN and NTg mice at 2 dpi. Concentra- tions are per milligram of organ tissue (n 3 mice/group). C, Quantification of IL-1�, IL-6, IL-10, and TNF� mRNA levels in brains of TMFN and NTg mice at 2 dpi. Quantifications are normalized to GAPDH mRNA (n 3 mice/group). Error bars represent mean � SEM, representative of triplicate experiments. Student’s t test or one-way ANOVA followed by Tukey’s multiple-comparison test. *p 0.05, **p 0.01, ***p 0.001, ****p 0.0001. ns, Nonsignificant. For further details on peripheral inflammation see Figure 2-1, available at https://doi.org/10.1523/JNEUROSCI.2324- 19.2020.f2-1. For the necessity of Mfn2 for neuroinflammation see Figure 2-2, available at https://doi.org/10.1523/JNEUROSCI.2324-19.2020.f2-2.

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https://doi.org/10.1523/JNEUROSCI.2324-19.2020.f4-1, which was expected. In systemic LPS models, mitochondrial fragmen- tation has been demonstrated in multiple peripheral tissues (Gonzalez et al., 2014; Hansen et al., 2015; Haileselassie et al., 2019). Consistently, the significant reduction in mitochondrial length could also be noted in neurons of NTg mice with LPS injection (Fig. 4 A, B). Mitochondria in TMFN neurons, however, still remained elongated after LPS challenge (Fig. 4 A, B), demon- strating that peripheral LPS-induced mitochondrial fragmenta- tion in neurons could be prevented by forced Mfn2 expression. We also investigated the expression of mitochondrial fission and fusion key regulators in brain and spinal cord tissues from TMFN and NTg mice with and without LPS injection. Immunoblot analysis confirmed significantly higher Mfn2 levels in TMFN mice. However, no significant changes in Mfn2 or other fusion regulators Mfn1 and Opa1 were noted in LPS versus PBS-injected NTg or TMFN mice (Fig. 4-1C,D, available at https://doi.org/ 10.1523/JNEUROSCI.2324-19.2020.f4-1). Fission related pro- teins Drp1 and MFF were also unaltered (Fig. 4-1C,D, available at https://doi.org/10.1523/JNEUROSCI.2324-19.2020.f4-1), sug- gesting that mitochondrial fragmentation is unlikely because of the altered expression of fission and fusion regulators. Of note, overall mitochondrial contents were similar among all samples as evidenced by the constant expression of mitochondrial marker VDAC1 (Fig. 4-1C,D, available at https://doi.org/10.1523/ JNEUROSCI.2324-19.2020.f4-1). These data collectively impli- cate that peripheral inflammation can induce mitochondrial fragmentation in neurons and that increased fusion protein Mfn2 can alleviate fragmented mitochondrial morphology caused by LPS.

Microglia activation inhibitor CX3CL1 is an indispensable factor for Mfn2-mediated microglia inhibition In the brain, CX3CL1 is produced by neurons and acts as the sole ligand of microglia expressed chemokine receptor CX3CR1 to mediate microglia activation in response to inflammatory stimuli such as LPS, IL-1�, and TNF� (Zujovic et al., 2000, 2001; Mizuno et al., 2003; Biber et al., 2007). Although quantitative PCR (qPCR) analyses found the greatly increased level of CX3CL1 mRNA in the TMFN brains, CX3CR1 mRNA was found to be unchanged (Fig. 5A), implying a likely specific effect of neuronal Mfn2 on CX3CL1 transcription. Notably, LPS injection induced strong downregulation of CX3CL1 mRNA in the brains of NTg, which was not observed in TMFN mouse brains, whereas CX3CR1 mRNA expression was similar between genotypes and injection groups (Fig. 5A). Consistently, the protein level of CX3CL1 was greatly augmented in TMFN brains and remained at similarly high levels after LPS injection, even though NTg mice with LPS injection only exhibited a trend, but not statistically significant, toward reduced expression of CX3CL1 at the protein level in brains (Fig. 5B). We next virally knocked down CX3CL1 in the hippocampi of TMFN and NTg mice and injected periph- eral LPS to determine whether CX3CL1 was critical for prevent- ing microglia activation in TMFN mice and whether its knockdown could exacerbate neuroinflammation in LPS- injected NTg mice. Astonishingly, CX3CL1 knockdown restored microglia activation in the hippocampi of TMFN mice with LPS and augmented microglia activation in LPS-injected NTg mice as evidenced by increased Iba1/IL-1� staining and increased num- ber of Iba1� microglia at the injection site compared with scrambled-control injected side (Fig. 5C,D, and Fig. 5-1, available

Figure 3. Microglia in TMFN mice are quiescent during peripheral LPS challenge. A, Representative IHC staining for Iba1 (microglia) in hippocampi of TMFN and NTg mice at 2 dpi. Enlarged images from boxed regions show individual microglia morphology (n 5 mice/group). B, Quantification of Iba1 intensity in frontal cortices of TMFN and NTg mice at 2 dpi from Iba1 IHC staining. AU, arbitrary units (n 5 mice/group). C, Representative brain CA1 region immunofluorescent staining for Iba1 (AF568; green) and nuclei (DAPI; blue) of TMFN and NTg mice at 2 dpi of LPS. Enlarged images from boxed regions show individual microglia morphology (n 4 mice/group). D, Quantification of average microglia process length and process number from Iba1 (AF568) immunoflu- orescent staining of brains from TMFN and NTg mice at 2 dpi. The longest process on each microglia and number of processes per microglia were averaged from images of the hippocampus and frontal cortex for each mouse. Data points represent the average process lengths or process numbers for individual mice (n 4 mice/group). Error bars represent mean � SEM, representative of triplicate experiments. Student’s t test or one-way ANOVA followed by Tukey’s multiple-comparison test. *p 0.05, **p 0.01, ****p 0.0001. ns, Nonsignificant. For further details on microglia and astrocyte activation see Figure 3-1, available at https://doi.org/10.1523/JNEUROSCI.2324-19.2020.f3-1. For the effect of microglia depletion see Figure 3-2, available at https://doi.org/10.1523/ JNEUROSCI.2324-19.2020.f3-2.

Harland et al. • Mitochondria for Neuroinflammation J. Neurosci., February 19, 2020 • 40(8):1756 –1765 • 1761

at https://doi.org/10.1523/JNEUROSCI.2324-19.2020.f5-1), supporting the necessity of CX3CL1 for Mfn2-mediated micro- glia inhibition. While further mechanistic insight is needed to identify how mitochondrial dynamics or Mfn2 expression regu- late CX3CL1 expression in neurons, these data suggest that forced Mfn2 expression in neurons drives expression of microglia inhibitory CX3CL1, potentially blocking peripheral-induced neuroinflammation.

Discussion In this study we demonstrate for the first time that genetic up- regulation of Mfn2 in neurons is sufficient to remarkably prevent sepsis lethality and sickness behavior induced by peripheral in- jection of lethal dose LPS. Interestingly, neuronal Mfn2 overex- pression resulted in the specific inhibition of microglia but not astrocytes. Likewise, LPS-induced IL-1� but not TNF�, IL-6, or IL-10 increase was also specifically suppressed by neuronal Mfn2. Because microglial inhibitor CX3CL1 produced by neurons was found greatly upregulated by neuronal Mfn2, Mfn2 likely acts as an unrecognized neuroinflammatory modulator in neurons. Neuronal Mfn2 ablation alone induces IL-1� release (Fig. 2-2 A–C, available at https://doi.org/10.1523/JNEUROSCI.2324-

19.2020.f2-2), implying its necessity for neuroinflammation. No- tably, Mfn2 is reduced in patients with AD or ALS (Wang et al., 2009, 2018). Therefore, neuronal Mfn2 may be a point of conver- gence for neuronal mitochondria dysfunction and neuroinflam- mation in neurodegeneration, worthy of further detailed investigation.

One of the most important and surprising findings of this study was that upregulation of Mfn2 in neurons was associated with almost completely abolished mortality in mice injected with a lethal dose of LPS. Mfn2 is only upregulated in the brain and spinal cord of TMFN mice. Even though the Thy1 promoter can drive transgene expression in enteric neurons (Goto et al., 2013), TMFN mouse peripheral tissues did not show increased Mfn2 expression (Fig. 1-1 A, B, available at https://doi.org/10.1523/ JNEUROSCI.2324-19.2020.f1-1). On top of these, TMFN mice exhibited LPS-induced peripheral inflammatory responses similar to NTg mice, together excluding the involvement of pe- ripheral immune system in the resistance of TMFN mice to LPS- induced lethality. Cardiac dysfunction is a prominent feature of septic shock in response to infection and has been implicated as an important component contributing to its high mortality (Ru-

Figure 4. Mfn2 overexpression alleviates peripheral LPS-induced mitochondrial fragmentation in neurons. A, Representative single plane (top) and 3D z-stack illustrations (middle/bottom) of immunofluorescent staining for VDAC1 (AF488; green) and nuclei (DAPI; blue) in CA1 neurons of TMFN and NTg mice at 2 dpi. Red boxes indicate region enlarged in the bottom panels (n 4 mice/group). B, Quantification of mitochondrial length in wide-field VDAC1 (AF488) immunofluorescent images of CA1 neurons of TMFN and NTg mice at 2 dpi. Measurements were averaged for individual CA1 neuronal images from each mouse. Data points represent the average mitochondrial length for individual mice (PBS injection: n 6 mice/group; LPS injection: n 5 mice/group). Error bars represent mean � SEM, representative of triplicate experiments. One-way ANOVA followed by Tukey’s multiple-comparison test. ***p 0.001. ns, Nonsignificant. For further details on mitochondrial dynamics see Figure 4-1, available at https://doi.org/10.1523/JNEUROSCI.2324-19.2020.f4-1. For neuronal viability see Figure 4-2, available at https://doi.org/10.1523/ JNEUROSCI.2324-19.2020.f4-2.

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diger and Singer, 2007). Although inflammatory cytokine release and Mfn2 expression were similar in NTg and TMFN heart tis- sues, there was clear absence of ischemic QT depression and a decrease in myocardial ischemia and infarction indicators HIF-1� and Ki-67 in TMFN mice (Fig. 1-2 A–F, available at https://doi.org/10.1523/JNEUROSCI.2324-19.2020.f1-2), indi- cating that neuronal Mfn2-regulated cardiac function, poten- tially through autonomic regulation, is likely an important mechanism for the suppression of lethality associated with septic shock in TMFN mice. In support of this notion, previous studies have identified autonomic control of myocardial dysfunction in LPS rodent models, particularly through cholinergic neurons of the sympathovagal system (Plaschke et al., 2018; Sallam et al., 2018; Ndongson-Dongmo et al., 2019). Nevertheless, additional work is still needed to clarify whether autonomic neurotransmis- sion is altered by Mfn2 overexpression in neurons. LPS has been reported to severely affect neural activity and dopamine release in reward-related brain regions in association with reduced motiva- tion and anhedonia (Felger et al., 2016). Accordingly, despite the absence of neuronal loss or altered expression of neuronal markers NeuN, MAP2, and synaptophysin in our results (Fig. 4-2 A–D, available at https://doi.org/10.1523/JNEUROSCI.2324- 19.2020.f4-2), mitigated LPS-induced sickness behavior was noted in TMFN mice. Therefore, Mfn2 may regulate neural ac- tivity and dopamine release in preventing the development of

cognitive and behavioral complications, worthy of further explo- ration. In addition to heart injury, systematic ischemic organ damage is present in murine LPS models (Cecconi et al., 2018). Because TMFN animals challenged with LPS displayed signifi- cantly alleviated bodyweight loss, future studies will also be inter- esting to investigate the possible Mfn2-mediated autonomic protection of other peripheral organs and tissues, which are known to be tightly controlled by the CNS and PNS.

Another interesting finding of the present study was the spe- cific inhibition of LPS-induced IL-1� but not IL-6, IL-10, or TNF� increase in the CNS by forced overexpression of neuronal Mfn2. IL-1� is a proinflammatory cytokine that is upregulated in AD and many neurodegenerative diseases, and believed to be the key player driving the neuroinflammatory process (Shaftel et al., 2008). By binding to its cognate receptor, IL-1� initiates a signal- ing cascade through the type I IL-1 receptor to activate NF-�B- dependent transcription of inflammatory gene expression (Weber et al., 2010). The majority of IL-1� research has been conducted on peripheral cells, but it appears that similar signal- ing mechanisms could be involved in IL-1�-mediated neuroin- flammation in CNS cells. IL-1� and other members of the IL-1 family can be constitutively synthesized by neural cells in the brain and have long been implied as neuromodulators in addi- tion to proinflammatory factors (Vitkovic et al., 2000). Although the specific cellular source and the regulation mechanisms for

Figure 5. CX3CL1 is upregulated and required for microglia inhibition in TMFN mice. A, CX3CL1 (top) and CX3CR1 (bottom) mRNA levels in brains of TMFN and NTg mice at 2 dpi were determined by qPCR. Fold changes were standardized to GAPDH mRNA for each mouse (n 3 mice/group). B, CX3CL1 protein levels in brains of TMFN and NTg mice at 2 dpi were assessed by ELISA. AU, Arbitrary units (n 4 mice/group). C, Representative whole brain and hippocampus IHC staining for Iba1 and IL-1� in LPS-injected TMFN mice with intrahippocampal AAV1-shCX3CL1 (right) and AAV1-Scrambled (left, control). Brains were isolated from TMFN and NTg mice 17 dpi of AAV1 and 2 dpi LPS. Arrowheads show hippocampal injection sites with increased Iba1� cell number and IL-1� staining in AAV1-shCX3CL1-injected mice (n 4 mice/group). D, Quantifications from IHC of Iba1� cell count (left), Iba1 intensity (middle), and IL-1� intensity (right) in hippocampal injection sites of TMFN and NTg mice from C (n 4 mice/group). Error bars represent mean � SEM, representative of triplicate experiments. Student’s t test and one-way ANOVA followed by Tukey’s multiple-comparison test. *p 0.05, **p 0.01, ***p 0.001, ****p 0.0001. ns, Nonsignificant. For further details on CX3CL1 ablation see Figure 5-1, available at https://doi.org/ 10.1523/JNEUROSCI.2324-19.2020.f5-1.

Harland et al. • Mitochondria for Neuroinflammation J. Neurosci., February 19, 2020 • 40(8):1756 –1765 • 1763

expression, cleavage, and release remain largely elusive, activated microglia are generally believed the to be the primary source of IL-1� in the brain (Rothwell and Luheshi, 2000). In support of this notion, microglia depletion was found to suppress LPS-induced loco- motive deficits (Fig. 3-2 A–D, available at https://doi.org/10.1523/ JNEUROSCI.2324-19.2020.f3-2). Indeed, TMFN mice demon- strated greatly abrogated basal microglia activation. Furthermore, despite the fact that astrocytes also play a critical role in regulating neuroinflammation and that IL-1� alone is capable of eliciting as- trocyte and microglia activation in the rodent brain (Rothwell and Luheshi, 2000; Felger et al., 2016), neuronal Mfn2 appears to have no effect on basal or LPS-induced astrocyte activation. Therefore, our results indicate that neuronal Mfn2 may control IL-1� expression or release by specifically participating in microglia activation.

CX3CR1 and its sole ligand CX3CL1 are critical mediators between neurons and microglia in neurodegenerative diseases (Finneran and Nash, 2019). Despite the dependence of neuro- protective or neurotoxic functions of the CX3CL1/CX3CR1 sig- naling pathway on microglial activation stimuli or pathological condition, a large body of evidence has implicated CX3CL1 as a potent inhibitor of microglial activation (Biber et al., 2007). Ex- citingly, we found significantly increased expression of CX3CL1 but not CX3CR1 in the CNS of TMFN mice. Knockdown of CX3CL1 was also sufficient to restore microglia activation and IL-1� release in hippocampi of LPS-injected TMFN mice. There- fore, a plausible mechanistic explanation for the specific inhibi- tory effects of neuronal Mfn2 on microglial activation and related cytokine release is that Mfn2 in neurons might contribute to the regulation of CX3CL1/CX3CR1 signaling by modulating the ex- pression of CX3CL1. As a predominant mitochondrial outer membrane protein, Mfn2 unlikely regulates CX3CL1 expression or transcription directly. Since LPS-induced mitochondrial frag- mentation was alleviated in TMFN mice, it is highly possible that neuronal Mfn2 may regulate CX3CL1 expression via mitochon- drial dynamics-dependent metabolism or the transport of neu- ronal factors required for CX3CL1 expression. However, considering the functional role of Mfn2 in ER and mitochondria tethering, autophagy, and calpastatin transport, we could not exclude the possibility that Mfn2 acts via other pathways to reg- ulate neuroinflammation via CX3CL1. Future detailed investiga- tion of the dependence of Mfn2-mediated CX3CL1 expression on mitochondrial fission and fusion dynamics and the sufficiency of mitochondrial fission and fusion dynamics for CX3CL1 regula- tion will provide a clear answer.

Together, these data suggest that Mfn2 in neurons contributes to the regulation of neuroinflammation. Although mitochon- drial dysfunction and neuroinflammation are two prominent pathological features of neurodegenerative diseases, whether and how neuronal mitochondria and neuroinflammation are interre- lated is largely unknown. Based on the remarkable suppression of LPS-induced neuroinflammation and neurodegeneration- associated mitochondrial dysfunction and dynamic abnormal- ities by neuronal Mfn2 (Wang et al., 2011, 2012, 2018), this study centered on Mfn2-mediated neuroinflammation reveals novel molecular mechanisms that are involved in both mito- chondrial dysfunction and neuroinflammation in neurodegenera- tive diseases. The pharmacological targeting of Mfn2 may present a novel treatment for neuroinflammation-associated diseases.

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