RESEARCH ARTICLE

Sarm1-mediated neurodegeneration within the enteric nervous system protects against local inflammation of the colon

  • Yue Sun 1 ,
  • Qi Wang 1 ,
  • Yi Wang 1 ,
  • Wenran Ren 6 ,
  • Ying Cao 1 ,
  • Jiali Li 2,7 ,
  • Xin Zhou 5 ,
  • Wei Fu 5 ,
  • Jing Yang , 1,2,3,4
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  • 1. State Key Laboratory of Membrane Biology, School of Life Sciences, Center for Life Sciences, Peking University, Beijing 100871, China
  • 2. IDG/McGovern Institute for Brain Research, Peking University, Beijing 100871, China
  • 3. Chinese Institute for Brain Research, Beijing 102206, China
  • 4. Shenzhen Bay Laboratory, Institute of Molecular Physiology, Shenzhen 518055, China
  • 5. Department of General Surgery, Peking University Third Hospital, Beijing 100191, China
  • 6. School of Medicine, Tsinghua University, Beijing 100084, China
  • 7. Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming 650223, China

Received date: 07 Jan 2021

Accepted date: 01 Mar 2021

Published date: 15 Aug 2021

Copyright

2021 The Author(s)

Abstract

Axonal degeneration is one of the key features of neurodegenerative disorders. In the canonical view, axonal degeneration destructs neural connections and promotes detrimental disease defects. Here, we assessed the enteric nervous system (ENS) of the mouse, nonhuman primate, and human by advanced 3D imaging. We observed the profound neurodegeneration of catecholaminergic axons in human colons with ulcerative colitis, and similarly, in mouse colons during acute dextran sulfate sodium-induced colitis. However, we unexpectedly revealed that blockage of such axonal degeneration by the Sarm1 deletion in mice exacerbated the colitis condition. In contrast, pharmacologic ablation or chemogenetic inhibition of catecholaminergic axons suppressed the colon inflammation. We further showed that the catecholaminergic neurotransmitter norepinephrine exerted a pro-inflammatory function by enhancing the expression of IL-17 cytokines. Together, this study demonstrated that Sarm1-mediated neurodegeneration within the ENS mitigated local inflammation of the colon, uncovering a previously-unrecognized beneficial role of axonal degeneration in this disease context.

Cite this article

Yue Sun , Qi Wang , Yi Wang , Wenran Ren , Ying Cao , Jiali Li , Xin Zhou , Wei Fu , Jing Yang . Sarm1-mediated neurodegeneration within the enteric nervous system protects against local inflammation of the colon[J]. Protein & Cell, 2021 , 12(8) : 621 -638 . DOI: 10.1007/s13238-021-00835-w

1
Brown MC, Lunn ER, Perry VH (1992) Consequences of slow Wallerian degeneration for regenerating motor and sensory axons. J Neurobiol 23:521–536

DOI

2
Cain DW, Cidlowski JA (2017)Immune regulation by glucocorticoids. Nat Rev Immunol 17:233–247

DOI

3
Chassaing B, Aitken JD, Malleshappa M, Vijay-Kumar M (2014) Dextran sulfate sodium (DSS)-induced colitis in mice. Curr Protoc Immunol 104:15–25

DOI

4
Coleman M (2005) Axon degeneration mechanisms: commonality amid diversity. Nat Rev Neurosci 6:889–898

DOI

5
Coleman MP, Hoke A (2020) Programmed axon degeneration: from mouse to mechanism to medicine. Nat Rev Neurosci 21:183–196

DOI

6
De Giorgio R, Guerrini S,Barbara G, Stanghellini V, De Ponti F, Corinaldesi R, Moses PL, Sharkey KA, Mawe GM (2004) Inflammatory neuropathies of the enteric nervous system. Gastroenterology 126:1872–1883

DOI

7
Erben U, Loddenkemper C, Doerfel K, Spieckermann S, Haller D, Heimesaat MM, Zeitz M, Siegmund B, Kuhl AA (2014) A guide to histomorphological evaluation of intestinal inflammation in mouse models. Int J Clin Exp Pathol 7:4557–4576

8
Essuman K, Summers DW, Sasaki Y, Mao X, DiAntonio A, Milbrandt J (2017) The SARM1 toll/interleukin-1 receptor domain possesses intrinsic NAD(+) cleavage activity that promotes pathological axonal degeneration. Neuron 93(1334–1343):

DOI

9
Figley MD, DiAntonio A (2020) The SARM1 axon degeneration pathway: control of the NAD(+) metabolome regulates axon survival in health and disease. Curr Opin Neurobiol 63:59–66

DOI

10
Furness JB (2012) The enteric nervous system and neurogastroenterology. Nat Rev Gastroenterol Hepatol 9:286–294

DOI

11
Gabanyi I, Muller PA, Feighery L, Oliveira TY, Costa-Pinto FA, Mucida D (2016) Neuro-immune interactions drive tissue programming in intestinal macrophages. Cell 164:378–391

DOI

12
Geisler S, Doan RA, Strickland A, Huang X, Milbrandt J, DiAntonio A (2016) Prevention of vincristine-induced peripheral neuropathy by genetic deletion of SARM1 in mice. Brain 139:3092–3108

DOI

13
Gerdts J, Summers DW, Sasaki Y, DiAntonio A, Milbrandt J (2013) Sarm1-mediated axon degeneration requires both SAM and TIR interactions. J Neurosci 33:13569–13580

DOI

14
Gerdts J, Brace EJ, Sasaki Y, DiAntonio A, Milbrandt J (2015) SARM1 activation triggers axon degeneration locally via NAD(+) destruction. Science 348:453–457

DOI

15
Glaser R, Kiecolt-Glaser JK (2005) Stress-induced immune dysfunction: implications for health. Nat Rev Immunol 5:243–251

DOI

16
Glass CK, Ogawa S (2006) Combinatorial roles of nuclear receptors in inflammation and immunity. Nat Rev Immunol 6:44–55

DOI

17
Godzik K, Coleman MP (2015) The axon-protective WLD(S) protein partially rescues mitochondrial respiration and glycolysis after axonal injury. J Mol Neurosci 55:865–871

DOI

18
Goyal RK, Hirano I (1996) The enteric nervous system. The New England journal of medicine 334:1106–1115

DOI

19
Graham KD, Lopez SH, Sengupta R, Shenoy A, Schneider S, Wright CM, Feldman M, Furth E, Valdivieso F, Lemke A (2020) Robust, 3-dimensional visualization of human colon enteric nervous system without tissue sectioning. Gastroenterology. 158(8):2221–2235

DOI

20
Gulbransen BD, Bashashati M, Hirota SA, Gui X, Roberts JA, MacDonald JA, Muruve DA, McKay DM, Beck PL, Mawe GM (2012) Activation of neuronal P2X7 receptor-pannexin-1 mediates death of enteric neurons during colitis. Nat Med 18:600–604

DOI

21
Hoopfer ED, McLaughlin T, Watts RJ, Schuldiner O, O’Leary DD, Luo L (2006) Wlds protection distinguishes axon degeneration following injury from naturally occurring developmental pruning. Neuron 50:883–895

DOI

22
Ito R, Kita M, Shin-Ya M, Kishida T, Urano A, Takada R, Sakagami J, Imanishi J,Iwakura Y, Okanoue T (2008) Involvement of IL-17A in the pathogenesis of DSS-induced colitis in mice. Biochem Biophys Res Commun 377:12–16

DOI

23
Ivanov II, McKenzie BS, Zhou L, Tadokoro CE, Lepelley A, Lafaille JJ, Cua DJ, Littman DR (2006) The orphan nuclear receptor RORgammat directs the differentiation program of proinflammatory IL-17+ T helper cells. Cell 126:1121–1133

DOI

24
Iwakura Y, Ishigame H, Saijo S, Nakae S(2011) Functional specialization of interleukin-17 family members. Immunity 34:149–162

DOI

25
Jiang Y, Liu Y, Lu H, Sun SC, Jin W, Wang X, Dong C (2018) Epigenetic activation during T helper 17 cell differentiation is mediated by Tripartite motif containing 28. Nat Commun 9:1424

DOI

26
Jiang Y, Liu T, Lee CH, Chang Q, Yang J, Zhang Z (2020) The NAD (+)-mediated self-inhibition mechanism of pro-neurodegenerative SARM1. Nature 588:658–663

DOI

27
Kiesler P, Fuss IJ, Strober W (2015) Experimental models of inflammatory bowel diseases. Cell Mol Gastroenterol Hepatol 1:154–170

DOI

28
Kim Y, Zhou P, Qian L, Chuang JZ, Lee J, Li C, Iadecola C, Nathan C, Ding A (2007) MyD88-5 links mitochondria, microtubules, and JNK3 in neurons and regulates neuronal survival. J Exp Med 204:2063–2074

DOI

29
Lai NY, Musser MA, Pinho-Ribeiro FA, Baral P,Jacobson A, Ma P,Potts DE, Chen Z, Paik D, Soualhi S (2020) Gut-innervating nociceptor neurons regulate peyer’s patch microfold cells and SFB levels to mediate salmonella host defense. Cell 180(33–49):

DOI

30
Liu T, Yang L, Han X, Ding X, Li J, Yang J (2020) Local sympathetic innervations modulate the lung innate immune responses. Science advances 6:eaay1497

DOI

31
Loreto A, Hill CS, Hewitt VL, Orsomando G, Angeletti C, Gilley J, Lucci C, Sanchez-Martinez A, Whitworth AJ, Conforti L (2020) Mitochondrial impairment activates the Wallerian pathway through depletion of NMNAT2 leading to SARM1-dependent axon degeneration. Neurobiol Dis 134:

DOI

32
Lunn ER, Perry VH, Brown MC, Rosen H, Gordon S (1989) Absence of wallerian degeneration does not hinder regeneration in peripheral nerve. Eur J Neurosci 1:27–33

DOI

33
Luo L, O’Leary DD (2005) Axon retraction and degeneration in development and disease. Annu Rev Neurosci 28:127–156

DOI

34
Mack TG, Reiner M, Beirowski B, Mi W, Emanuelli M, Wagner D, Thomson D, Gillingwater T, Court F, Conforti L (2001) Wallerian degeneration of injured axons and synapses is delayed by a Ube4b/Nmnat chimeric gene. Nat Neurosci 4:1199–1206

DOI

35
Madden KS, Sanders VM, Felten DL (1995) Catecholamine influences and sympathetic neural modulation of immune responsiveness. Annu Rev Pharmacol Toxicol 35:417–448

DOI

36
Matheis F, Muller PA, Graves CL, Gabanyi I,Kerner ZJ, Costa-Borges D, Ahrends T, Rosenstiel P, Mucida D (2020) Adrenergic signaling in muscularis macrophages limits infection-induced neuronal loss. Cell 180(64–78):

DOI

37
Miossec P, Kolls JK (2012) Targeting IL-17 and TH17 cells in chronic inflammation. Nat Rev Drug Discov 11:763–776

DOI

38
Murthy SN, Cooper HS, Shim H, Shah RS, Ibrahim SA, Sedergran DJ (1993) Treatment of dextran sulfate sodium-induced murine colitis by intracolonic cyclosporin. Dig Dis Sci 38:1722–1734

DOI

39
Neckel PH, Mattheus U, Hirt B, Just L, Mack AF (2016) Large-scale tissue clearing (PACT): Technical evaluation and new perspectives in immunofluorescence, histology, and ultrastructure. Sci Rep 6:34331

DOI

40
Neukomm LJ, Freeman MR (2014) Diverse cellular and molecular modes of axon degeneration. Trends Cell Biol 24:515–523

DOI

41
Obermayr F, Hotta R, Enomoto H, Young HM (2013) Development and developmental disorders of the enteric nervous system. Nat Rev Gastroenterol Hepatol 10:43–57

DOI

42
Osterloh JM, Yang J, Rooney TM, Fox AN, Adalbert R, Powell EH, Sheehan AE, Avery MA, Hackett R, Logan MA (2012) dSarm/Sarm1 is required for activation of an injury-induced axon death pathway. Science 337:481–484

DOI

43
Padgett DA, Glaser R (2003) How stress influences the immune response. Trends Immunol 24:444–448

DOI

44
Rao M, Gershon MD (2016) The bowel and beyond: the enteric nervous system in neurological disorders. Nat Rev Gastroenterol Hepatol 13:517–528

DOI

45
Schraml BU, Hildner K, Ise W, Lee WL, Smith WA, Solomon B, Sahota G, Sim J, Mukasa R, Cemerski S (2009) The AP-1 transcription factor Batf controls T(H)17 differentiation. Nature 460:405–409

DOI

46
Simon DJ, Weimer RM, McLaughlin T, Kallop D, Stanger K, Yang J, O’Leary DD, Hannoush RN, Tessier-Lavigne M (2012) A caspase cascade regulating developmental axon degeneration. J Neurosci 32:17540–17553

DOI

47
Straub RH, Grum F, Strauch U, Capellino S, Bataille F, Bleich A, Falk W, Scholmerich J,Obermeier F (2008) Anti-inflammatory role of sympathetic nerves in chronic intestinal inflammation. Gut 57:911–921

DOI

48
Talbot J, Hahn P, Kroehling L,Nguyen H, Li D, Littman DR (2020) Feeding-dependent VIP neuron-ILC3 circuit regulates the intestinal barrier. Nature 579:575–580

DOI

49
Tang C,Kakuta S, Shimizu K, Kadoki M, Kamiya T, Shimazu T,Kubo S, Saijo S, Ishigame H, Nakae S (2018) Suppression of IL- 17F, but not of IL-17A, provides protection against colitis by inducing Treg cells through modification of the intestinal microbiota. Nat Immunol 19:755–765

DOI

50
Wang J, Zhai Q, Chen Y, Lin E, Gu W,McBurney MW, He Z (2005) A local mechanism mediates NAD-dependent protection of axon degeneration. J Cell Biol 170:349–355

DOI

51
Wang JT, Medress ZA, Barres BA (2012) Axon degeneration: molecular mechanisms of a self-destruction pathway. J Cell Biol 196:7–18

DOI

52
Wang Q, Liu K, Yang L, Wang H, Yang J(2019) BoneClear: wholetissue immunolabeling of the intact mouse bones for 3D imaging of neural anatomy and pathology. Cell Res 29:870–872

DOI

53
Webster JI, Tonelli L, Sternberg EM (2002) Neuroendocrine regulation of immunity. Annu Rev Immunol 20:125–163

DOI

54
Whitmore AV, Lindsten T,Raff MC, Thompson CB (2003) The proapoptotic proteins Bax and Bak are not involved in Wallerian degeneration. Cell Death Differ 10:260–261

DOI

55
Wong DL, Tai TC, Wong-Faull DC, Claycomb R, Meloni EG, Myers KM, Carlezon WA Jr,Kvetnansky R (2012) Epinephrine: a short- and long-term regulator of stress and development of illness : a potential new role for epinephrine in stress. Cell Mol Neurobiol 32:737–748

DOI

56
Yang XO, Chang SH, Park H, Nurieva R, Shah B, Acero L, Wang YH, Schluns KS, Broaddus RR, Zhu Z (2008) Regulation of inflammatory responses by IL-17F. J Exp Med 205:1063–1075

DOI

57
Yang J, Wu Z, Renier N, Simon DJ, Uryu K, Park DS, Greer PA, Tournier C, Davis RJ, Tessier-Lavigne M (2015) Pathological axonal death through a MAPK cascade that triggers a local energy deficit. Cell 160:161–176

DOI

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