Evidence map›Paper›PMID 34593632›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2021

Circuit-specific enteric glia regulate intestinal motor neurocircuits.

Mohammad M Ahmadzai, Luisa Seguella, Brian D Gulbransen

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
–field-weighted citation impact
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

36 citing papers in PubMed.

  1. Article
  2. Article
  3. Macrophage-glia interactions regulate immune damage to enteric neurons during West Nile virus infection.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  4. Transgenic Mouse Models to Study Enteric Glia.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  5. Article
  6. Review
  7. Calcium Imaging Studies in Enteric Glia.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  8. Review
  9. Review
  10. Review
  11. Review
  12. Purinergic P2YPurinergic signalling · 2025
    Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Unique properties of proximal and distal colon reflect distinct motor functions.American journal of physiology. Gastrointestinal and liver physiology · 2025
    Review
  18. The Physiology of Enteric Glia.Annual review of physiology · 2025
    Review
  19. Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Mohammad M AhmadzaiDepartment of Physiology, Neuroscience Program, Michigan State University, East Lansing, MI 48824.ORCID 0000-0002-3715-8587
Luisa SeguellaDepartment of Physiology, Neuroscience Program, Michigan State University, East Lansing, MI 48824.ORCID 0000-0003-2346-9912
Brian D GulbransenDepartment of Physiology, Neuroscience Program, Michigan State University, East Lansing, MI 48824; gulbrans@msu.edu.ORCID 0000-0003-1145-3227

Funding

Role of enteric glia in the death of neurons during gut inflammationR01DK103723 · NIDDK · MICHIGAN STATE UNIVERSITY · PI BRIAN D. GULBRANSEN · 2015 to 2026
$4.7M
Enteric glia and visceral painR01DK120862 · NIDDK · MICHIGAN STATE UNIVERSITY · PI BRIAN D. GULBRANSEN · 2019 to 2026
$3.0M
NIDDK NIH HHS R01 DK103723NIDDK NIH HHS R01 DK120862
6 · The paper itself

Abstract

Glia in the central nervous system exert precise spatial and temporal regulation over neural circuitry on a synapse-specific basis, but it is unclear if peripheral glia share this exquisite capacity to sense and modulate circuit activity. In the enteric nervous system (ENS), glia control gastrointestinal motility through bidirectional communication with surrounding neurons. We combined glial chemogenetics with genetically encoded calcium indicators expressed in enteric neurons and glia to study network-level activity in the intact myenteric plexus of the proximal colon. Stimulation of neural fiber tracts projecting in aboral, oral, and circumferential directions activated distinct populations of enteric glia. The majority of glia responded to both oral and aboral stimulation and circumferential pathways, while smaller subpopulations were activated only by ascending and descending pathways. Cholinergic signaling functionally specifies glia to the descending circuitry, and this network plays an important role in repressing the activity of descending neural pathways, with some degree of cross-inhibition imposed upon the ascending pathway. Glial recruitment by purinergic signaling functions to enhance activity within ascending circuit pathways and constrain activity within descending networks. Pharmacological manipulation of glial purinergic and cholinergic signaling differentially altered neuronal responses in these circuits in a sex-dependent manner. Collectively, our findings establish that the balance between purinergic and cholinergic signaling may differentially control specific circuit activity through selective signaling between networks of enteric neurons and glia. Thus, enteric glia regulate the ENS circuitry in a network-specific manner, providing profound insights into the functional breadth and versatility of peripheral glia.

Indexed as

AnimalsCell CommunicationEnteric Nervous SystemFemaleGastrointestinal MotilityMaleMiceMyenteric PlexusNeurogliaNeuronsSignal Transductionautonomicenteric nervous systemgastrointestinalglianeuroglia

Identifiers

PMID34593632
PMCPMC8501758

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.