A neuroprotective astrocyte state is induced by neuronal signal EphB1 but fails in ALS models
Jazyk angličtina Země Anglie, Velká Británie Médium electronic
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
MR/M02492X/1
Medical Research Council - United Kingdom
MR/P008658/1
Medical Research Council - United Kingdom
101149/Z/13/A
Wellcome Trust - United Kingdom
PubMed
29079839
PubMed Central
PMC5660125
DOI
10.1038/s41467-017-01283-z
PII: 10.1038/s41467-017-01283-z
Knihovny.cz E-zdroje
- MeSH
- amyotrofická laterální skleróza metabolismus MeSH
- antiflogistika farmakologie MeSH
- astrocyty cytologie metabolismus MeSH
- axony metabolismus MeSH
- interleukin-6 metabolismus MeSH
- kultivované buňky MeSH
- lidé MeSH
- modely nemocí na zvířatech MeSH
- motorické neurony metabolismus MeSH
- myši inbrední C57BL MeSH
- myši MeSH
- nervus ischiadicus metabolismus MeSH
- neurony metabolismus MeSH
- neuroprotekce MeSH
- receptor EphB1 metabolismus MeSH
- signální transdukce MeSH
- transkripční faktor STAT3 metabolismus MeSH
- transkriptom MeSH
- zánět MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- antiflogistika MeSH
- interleukin-6, mouse MeSH Prohlížeč
- interleukin-6 MeSH
- receptor EphB1 MeSH
- Stat3 protein, mouse MeSH Prohlížeč
- transkripční faktor STAT3 MeSH
Astrocyte responses to neuronal injury may be beneficial or detrimental to neuronal recovery, but the mechanisms that determine these different responses are poorly understood. Here we show that ephrin type-B receptor 1 (EphB1) is upregulated in injured motor neurons, which in turn can activate astrocytes through ephrin-B1-mediated stimulation of signal transducer and activator of transcription-3 (STAT3). Transcriptional analysis shows that EphB1 induces a protective and anti-inflammatory signature in astrocytes, partially linked to the STAT3 network. This is distinct from the response evoked by interleukin (IL)-6 that is known to induce both pro inflammatory and anti-inflammatory processes. Finally, we demonstrate that the EphB1-ephrin-B1 pathway is disrupted in human stem cell derived astrocyte and mouse models of amyotrophic lateral sclerosis (ALS). Our work identifies an early neuronal help-me signal that activates a neuroprotective astrocytic response, which fails in ALS, and therefore represents an attractive therapeutic target.
Addenbrooke's Hospital Cambridge University Hospitals Hills Road Cambridge CB2 0QQ UK
The Francis Crick Institute 1 Midland Road London NW1 1AT UK
Waisman Center University of Wisconsin 1500 Highland Avenue Madison WI 53705 USA
Zobrazit více v PubMed
Tyzack GE, et al. Astrocyte response to motor neuron injury promotes structural synaptic plasticity via STAT3-regulated TSP-1 expression. Nat. Commun. 2014;5:4294. doi: 10.1038/ncomms5294. PubMed DOI PMC
Faulkner JR, et al. Reactive astrocytes protect tissue and preserve function after spinal cord injury. J. Neurosci. 2004;24:2143–2155. doi: 10.1523/JNEUROSCI.3547-03.2004. PubMed DOI PMC
Anderson MA, et al. Astrocyte scar formation aids central nervous system axon regeneration. Nature. 2016;532:195–200. doi: 10.1038/nature17623. PubMed DOI PMC
Burda JE, Sofroniew MV. Reactive gliosis and the multicellular response to CNS damage and disease. Neuron. 2014;81:229–248. doi: 10.1016/j.neuron.2013.12.034. PubMed DOI PMC
Yamanaka K, et al. Astrocytes as determinants of disease progression in inherited amyotrophic lateral sclerosis. Nat. Neurosci. 2008;11:251–253. doi: 10.1038/nn2047. PubMed DOI PMC
Di Giorgio FP, Carrasco Ma, Siao MC, Maniatis T, Eggan K. Non-cell autonomous effect of glia on motor neurons in an embryonic stem cell-based ALS model. Nat. Neurosci. 2007;10:608–614. doi: 10.1038/nn1885. PubMed DOI PMC
Nagai M, et al. Astrocytes expressing ALS-linked mutated SOD1 release factors selectively toxic to motor neurons. Nat. Neurosci. 2007;10:615–622. doi: 10.1038/nn1876. PubMed DOI PMC
Zamanian JL, et al. Genomic analysis of reactive astrogliosis. J. Neurosci. 2012;32:6391–6410. doi: 10.1523/JNEUROSCI.6221-11.2012. PubMed DOI PMC
Sofroniew MV. Multiple roles for astrocytes as effectors of cytokines and inflammatory mediators. Neuroscientist. 2013;20:160–172. doi: 10.1177/1073858413504466. PubMed DOI
Streit WJ, Hurley SD, McGraw TS, Semple-Rowland SL. Comparative evaluation of cytokine profiles and reactive gliosis supports a critical role for interleukin-6 in neuron-glia signaling during regeneration. J. Neurosci. Res. 2000;61:10–20. doi: 10.1002/1097-4547(20000701)61:1<10::AID-JNR2>3.0.CO;2-E. PubMed DOI
Aldskogius H, Kozlova EN. Central neuron-glial and glial-glial interactions following axon injury. Prog. Neurobiol. 1998;55:1–26. doi: 10.1016/S0301-0082(97)00093-2. PubMed DOI
Murphy PG, Borthwick LS, Johnston RS, Kuchel G, Richardson PM. Nature of the retrograde signal from injured nerves that induces interleukin-6 mRNA in neurons. J. Neurosci. 1999;19:3791–3800. PubMed PMC
Xin J, et al. IL-10 within the CNS is necessary for CD4+ T cells to mediate neuroprotection. Brain Behav. Immun. 2011;25:820–829. doi: 10.1016/j.bbi.2010.08.004. PubMed DOI PMC
Lu T-Y, et al. Axon degeneration induces glial responses through Draper-TRAF4-JNK signalling. Nat. Commun. 2017;8:14355. doi: 10.1038/ncomms14355. PubMed DOI PMC
Liddelow SA, et al. Neurotoxic reactive astrocytes are induced by activated microglia. Nature. 2017;541:481–487. doi: 10.1038/nature21029. PubMed DOI PMC
Kania A, Klein R. Mechanisms of ephrin–Eph signalling in development, physiology and disease. Nat. Rev. Mol. Cell Biol. 2016;17:240–256. doi: 10.1038/nrm.2015.16. PubMed DOI
Wang Y, et al. Induction of ephrin-B1 and EphB receptors during denervation-induced plasticity in the adult mouse hippocampus. Eur. J. Neurosci. 2005;21:2336–2346. doi: 10.1111/j.1460-9568.2005.04093.x. PubMed DOI
Song X-J, et al. Upregulation and redistribution of ephrinB and EphB receptor in dorsal root ganglion and spinal dorsal horn neurons after peripheral nerve injury and dorsal rhizotomy. Eur. J. Pain. 2008;12:1031–1039. doi: 10.1016/j.ejpain.2008.01.011. PubMed DOI
Coulthard MG, et al. Eph/Ephrin signaling in injury and inflammation. Am. J. Pathol. 2012;181:1493–1503. doi: 10.1016/j.ajpath.2012.06.043. PubMed DOI
Pasquale EB. Eph-ephrin bidirectional signaling in physiology and disease. Cell. 2008;133:38–52. doi: 10.1016/j.cell.2008.03.011. PubMed DOI
Van Hoecke A, et al. EPHA4 is a disease modifier of amyotrophic lateral sclerosis in animal models and in humans. Nat. Med. 2012;18:1418–1422. doi: 10.1038/nm.2901. PubMed DOI
Cissé M, Checler F. Eph receptors: new players in Alzheimer’s disease pathogenesis. Neurobiol. Dis. 2015;73:137–149. doi: 10.1016/j.nbd.2014.08.028. PubMed DOI
Kim Y-S, et al. Correction of humoral derangements from mutant superoxide dismutase 1 spinal cord. Ann. Neurol. 2006;60:716–728. doi: 10.1002/ana.21034. PubMed DOI
Kim RB, Irvin CW, Tilva KR, Mitchell CS. State of the field: an informatics-based systematic review of the SOD1-G93A amyotrophic lateral sclerosis transgenic mouse model. Amyotroph. Lateral Scler. Frontotemporal. Degener. 2015;8421:1–14. PubMed PMC
Sun S, et al. Translational profiling identifies a cascade of damage initiated in motor neurons and spreading to glia in mutant SOD1-mediated ALS. Proc. Natl Acad. Sci. USA. 2015;112:E6993–E7002. doi: 10.1073/pnas.1520639112. PubMed DOI PMC
Papadimitriou D, et al. Inflammation in ALS and SMA: sorting out the good from the evil. Neurobiol. Dis. 2010;37:493–502. doi: 10.1016/j.nbd.2009.10.005. PubMed DOI PMC
Frakes AE, et al. Microglia induce motor neuron death via the classical NF-κB pathway in amyotrophic lateral sclerosis. Neuron. 2014;81:1009–1023. doi: 10.1016/j.neuron.2014.01.013. PubMed DOI PMC
Mesnard Na, Sanders VM, Jones KJ. Differential gene expression in the axotomized facial motor nucleus of presymptomatic SOD1 mice. J. Comp. Neurol. 2011;519:3488–3506. doi: 10.1002/cne.22718. PubMed DOI PMC
Shibata N, et al. Activation of STAT3 and inhibitory effects of pioglitazone on STAT3 activity in a mouse model of SOD1-mutated amyotrophic lateral sclerosis. Neuropathology. 2010;30:353–360. doi: 10.1111/j.1440-1789.2009.01078.x. PubMed DOI
Tyzack G, Lakatos A, Patani R. Human stem cell-derived astrocytes: specification and relevance for neurological disorders. Curr. Stem Cell Rep. 2016;2:236–247. doi: 10.1007/s40778-016-0049-1. PubMed DOI PMC
Scheller J, Chalaris A, Schmidt-Arras D, Rose-John S. The pro- and anti-inflammatory properties of the cytokine interleukin-6. Biochim. Biophys. Acta. 2011;1813:878–888. doi: 10.1016/j.bbamcr.2011.01.034. PubMed DOI
Wootz H, Enjin A, Wallén-Mackenzie Å, Lindholm D, Kullander K. Reduced VGLUT2 expression increases motor neuron viability in Sod1G93A mice. Neurobiol. Dis. 2010;37:58–66. doi: 10.1016/j.nbd.2009.09.006. PubMed DOI
Courville J. The nucleus of the facial nerve: the relation be- tween cellular groups and peripheral branches of the facial nerve. Brain. Res. 1966;1:338–354. doi: 10.1016/0006-8993(66)90126-0. PubMed DOI
Sherwood CC. Comparative anatomy of the facial motor nucleus in mammals, with an analysis of neuron numbers in primates. Anat. Rec. 2005;287A:1067–1079. doi: 10.1002/ar.a.20259. PubMed DOI
Herrmann JE, et al. STAT3 is a critical regulator of astrogliosis and scar formation after spinal cord injury. J. Neurosci. 2008;28:7231–7243. doi: 10.1523/JNEUROSCI.1709-08.2008. PubMed DOI PMC
Sarafian TA, et al. Disruption of astrocyte STAT3 signaling decreases mitochondrial function and increases oxidative stress in vitro. PLoS ONE. 2010;5:e9532. doi: 10.1371/journal.pone.0009532. PubMed DOI PMC
Baorto DM, Mellado W, Shelanski ML. Astrocyte process growth induction by actin breakdown. J. Cell. Biol. 1992;117:357–367. doi: 10.1083/jcb.117.2.357. PubMed DOI PMC
Nicchia GP, et al. New possible roles for aquaporin-4 in astrocytes: cell cytoskeleton and functional relationship with connexin43. FASEB J. 2005;19:1674–1676. PubMed
Pekny M, Nilsson M. Astrocyte activation and reactive gliosis. Glia. 2005;50:427–434. doi: 10.1002/glia.20207. PubMed DOI
Falsig J, Pörzgen P, Lund S, Schrattenholz A, Leist M. The inflammatory transcriptome of reactive murine astrocytes and implications for their innate immune function. J. Neurochem. 2006;96:893–907. doi: 10.1111/j.1471-4159.2005.03622.x. PubMed DOI
Sofroniew MV. Astrogliosis. Cold Spring Harb. Perspect. Biol. 2015;7:a020420. doi: 10.1101/cshperspect.a020420. PubMed DOI PMC
Hall CE, et al. Progressive motor neuron pathology and the role of astrocytes in a human stem cell model of VCP-related ALS. Cell Rep. 2017;19:1739–1749. doi: 10.1016/j.celrep.2017.05.024. PubMed DOI PMC
Ferraiuolo L, et al. Dysregulation of astrocyte-motoneuron cross-talk in mutant superoxide dismutase 1-related amyotrophic lateral sclerosis. Brain. 2011;134:2627–2641. doi: 10.1093/brain/awr193. PubMed DOI PMC
Kawase T, et al. PH domain-only protein PHLDA3 is a p53-regulated repressor of Akt. Cell. 2009;136:535–550. doi: 10.1016/j.cell.2008.12.002. PubMed DOI
Viúdez A, et al. A new immunohistochemistry prognostic score (IPS) for recurrence and survival in resected pancreatic neuroendocrine tumors (PanNET) Oncotarget. 2016;7:24950–24961. doi: 10.18632/oncotarget.7436. PubMed DOI PMC
Sofroniew MV. Molecular dissection of reactive astrogliosis and glial scar formation. Trends Neurosci. 2009;32:638–647. doi: 10.1016/j.tins.2009.08.002. PubMed DOI PMC
Pasquale EB. Eph–ephrin promiscuity is now crystal clear. Nat. Neurosci. 2004;7:417–418. doi: 10.1038/nn0504-417. PubMed DOI
Lauterbach J, Klein R. Release of full-length EphB2 receptors from hippocampal neurons to cocultured glial cells. J. Neurosci. 2006;26:11575–11581. doi: 10.1523/JNEUROSCI.2697-06.2006. PubMed DOI PMC
Cowan CA, Henkemeyer M. The SH2/SH3 adaptor Grb4 transduces B-ephrin reverse signals. Nature. 2001;413:174–179. doi: 10.1038/35093123. PubMed DOI
Bong Y-S, et al. ephrinB1 signals from the cell surface to the nucleus by recruitment of STAT3. Proc. Natl Acad. Sci. USA. 2007;104:17305–17310. doi: 10.1073/pnas.0702337104. PubMed DOI PMC
Lo U, et al. p38α (MAPK14) critically regulates the immunological response and the production of specific cytokines and chemokines in astrocytes. Sci. Rep. 2014;4:7405. doi: 10.1038/srep07405. PubMed DOI PMC
Hutchins AP, Poulain S, Miranda-Saavedra D. Genome-wide analysis of STAT3 binding in vivo predicts effectors of the anti-inflammatory response in macrophages. Blood. 2012;119:e110–119. doi: 10.1182/blood-2011-09-381483. PubMed DOI
Oliva AA, Kang Y, Sanchez-Molano J, Furones C, Atkins CM. STAT3 signaling after traumatic brain injury. J. Neurochem. 2012;120:710–720. doi: 10.1111/j.1471-4159.2011.07610.x. PubMed DOI
Sofroniew MV. Neuroscientist reactive astrocytes in neural repair and protection. Neuroscientist. 2005;11:400–407. doi: 10.1177/1073858405278321. PubMed DOI
Stevens B, et al. The classical complement cascade mediates CNS synapse elimination. Cell. 2007;131:1164–1178. doi: 10.1016/j.cell.2007.10.036. PubMed DOI
Chung W-S, et al. Astrocytes mediate synapse elimination through MEGF10 and MERTK pathways. Nature. 2013;504:394–400. doi: 10.1038/nature12776. PubMed DOI PMC
Ziegenfuss JS, Doherty J, Freeman MR. Distinct molecular pathways mediate glial activation and engulfment of axonal debris after axotomy. Nat. Neurosci. 2012;15:979–987. doi: 10.1038/nn.3135. PubMed DOI PMC
Moran LB, Graeber MB. The facial nerve axotomy model. Brain Res. Rev. 2004;44:154–178. doi: 10.1016/j.brainresrev.2003.11.004. PubMed DOI
Molofsky AV, et al. Astrocyte-encoded positional cues maintain sensorimotor circuit integrity. Nature. 2014;509:189–194. doi: 10.1038/nature13161. PubMed DOI PMC
Nikolakopoulou AM, et al. Astrocytic ephrin-B1 regulates synapse remodeling following traumatic brain injury. ASN Neuro. 2016;8:1759091416630220. doi: 10.1177/1759091416630220. PubMed DOI PMC
Sekizawa T, et al. Cerebrospinal fluid interleukin 6 in amyotrophic lateral sclerosis: immunological parameter and comparison with inflammatory and non-inflammatory central nervous system diseases. J. Neurol. Sci. 1998;154:194–199. doi: 10.1016/S0022-510X(97)00228-1. PubMed DOI
Han CY, Lim SW, Koo JH, Kim W, Kim SG. PHLDA3 overexpression in hepatocytes by endoplasmic reticulum stress via IRE1–Xbp1s pathway expedites liver injury. Gut. 2016;65:1377–1388. doi: 10.1136/gutjnl-2014-308506. PubMed DOI PMC
Ikiz B, et al. The regulatory machinery of neurodegeneration in in vitro models of amyotrophic lateral sclerosis. Cell Rep. 2015;12:335–345. doi: 10.1016/j.celrep.2015.06.019. PubMed DOI PMC
Heneka MT, et al. Neuroinflammation in Alzheimer’s disease. Lancet Neurol. 2015;14:388–405. doi: 10.1016/S1474-4422(15)70016-5. PubMed DOI PMC
Crisafulli, S. G., Brajkovic, S., Cipolat Mis, M. S., Parente, V. & Corti, S. Therapeutic strategies under development targeting inflammatory mechanisms in amyotrophic lateral sclerosis. Mol. Neurobiol. 10.1007/s12035-017-0532-4 (2017). PubMed
Lakatos A. State-of-art modelling of inflammatory astrocyte-synapse interactions in injury and amyotrophic lateral sclerosis. Neural Regen. Res. 2017;12:75–76. doi: 10.4103/1673-5374.198977. PubMed DOI PMC
Phani S, Re DB, Przedborski S. The role of the innate immune system in ALS. Front. Pharmacol. 2012;3:150. doi: 10.3389/fphar.2012.00150. PubMed DOI PMC
Lam L, et al. Anti-inflammatory therapies of amyotrophic lateral sclerosis guided by immune pathways. Am. J. Neurodegener. Dis. 2015;4:28–39. PubMed PMC
Kerstetter AE, Miller RH. Isolation and culture of spinal cord astrocytes. Methods Mol. Biol. 2012;814:93–104. doi: 10.1007/978-1-61779-452-0_7. PubMed DOI PMC
Beaudet M-J, et al. High yield extraction of pure spinal motor neurons, astrocytes and microglia from single embryo and adult mouse spinal cord. Sci. Rep. 2015;5:16763. doi: 10.1038/srep16763. PubMed DOI PMC
Mulvey CM, et al. Using hyperLOPIT to perform high-resolution mapping of the spatial proteome. Nat. Protoc. 2017;12:1110–1135. doi: 10.1038/nprot.2017.026. PubMed DOI
Young MD, Wakefield MJ, Smyth GK, Oshlack A. Gene ontology analysis for RNA-seq: accounting for selection bias. Genome. Biol. 2010;11:R14. doi: 10.1186/gb-2010-11-2-r14. PubMed DOI PMC
Vaquerizas JM, Kummerfeld SK, Teichmann SA, Luscombe NM. A census of human transcription factors: function, expression and evolution. Nat. Rev. Genet. 2009;10:252–263. doi: 10.1038/nrg2538. PubMed DOI
Glial Cells-The Strategic Targets in Amyotrophic Lateral Sclerosis Treatment