Evidence map›Paper›PMID 33871822›Full record

ArticleProtein & cell2021

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

Yue Sun, Qi Wang, Yi Wang, Wenran Ren, Ying Cao, Jiali Li, Xin Zhou, Wei Fu, Jing Yang

Open access · diamondAbstract read
In one paragraph

Article in Protein & cell, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.0field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Blocking the mCellular & molecular immunology · 2026
    Article
  4. Peripheral Neuropathy in Metabolic Stress.International journal of molecular sciences · 2026
    Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Imaging the enteric nervous system.Frontiers in neuroanatomy · 2025
    Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. NADCell insight · 2022
    Review
  16. SARM1 can be a potential therapeutic target for spinal cord injury.Cellular and molecular life sciences : CMLS · 2022
    Review
  17. Editorial: Neuroimmune Interactions in Peripheral Neuropathy.Frontiers in molecular neuroscience · 2022
    Article
  18. Article
  19. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Yue Sun *State Key Laboratory of Membrane Biology, School of Life Sciences, Center for Life Sciences, Peking University, Beijing, 100871, China.
Qi Wang *State Key Laboratory of Membrane Biology, School of Life Sciences, Center for Life Sciences, Peking University, Beijing, 100871, China.
Yi WangState Key Laboratory of Membrane Biology, School of Life Sciences, Center for Life Sciences, Peking University, Beijing, 100871, China.
Wenran RenSchool of Medicine, Tsinghua University, Beijing, 100084, China.
Ying CaoState Key Laboratory of Membrane Biology, School of Life Sciences, Center for Life Sciences, Peking University, Beijing, 100871, China.
Jiali LiIDG/McGovern Institute for Brain Research, Peking University, Beijing, 100871, China.
Xin ZhouDepartment of General Surgery, Peking University Third Hospital, Beijing, 100191, China.
Wei FuDepartment of General Surgery, Peking University Third Hospital, Beijing, 100191, China.
Jing YangState Key Laboratory of Membrane Biology, School of Life Sciences, Center for Life Sciences, Peking University, Beijing, 100871, China. jing.yang@pku.edu.cn.ORCID 0000-0002-2048-735X
Peking University · CNKunming Institute of Zoology · CNTsinghua University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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, non-human 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.

Indexed as

AnimalsArmadillo Domain ProteinsCatecholaminesColitis, UlcerativeColonCytoskeletal ProteinsDextran SulfateDisease Models, AnimalEnteric Nervous SystemGene Expression RegulationHumansImaging, Three-DimensionalInterleukin-17Macaca mulattaMaleMiceArmadillo Domain ProteinsCatecholaminesCytoskeletal ProteinsDextran SulfateIl17a protein, mouseInterleukin-17NorepinephrineNuclear Receptor Subfamily 1, Group F, Member 3Rorc protein, mouseSARM1 protein, mouseTumor Necrosis Factor-alpha3D imagingaxonal degenerationcatecholaminergic axonscolitisenteric nervous systemneurodegenerationSarm1

Identifiers

PMID33871822
PMCPMC8310542
OpenAlexW3154970207

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.