The DOI matches its Crossref record; 177 of the 177 references it cites were found in a registry or an index.
Enteric glial biology, intercellular signalling and roles in gastrointestinal disease
Open accessAbstract
One of the most transformative developments in neurogastroenterology is the realization that many functions normally attributed to enteric neurons involve interactions with enteric glial cells: a large population of peripheral neuroglia associated with enteric neurons throughout the gastrointestinal tract. The notion that glial cells function solely as passive support cells has been refuted by compelling evidence that demonstrates that enteric glia are important homeostatic cells of the intestine. Active signalling mechanisms between enteric glia and neurons modulate gastrointestinal reflexes and, in certain circumstances, function to drive neuroinflammatory processes that lead to long-term dysfunction. Bidirectional communication between enteric glia and immune cells contributes to gastrointestinal immune homeostasis, and crosstalk between enteric glia and cancer stem cells regulates tumorigenesis. These neuromodulatory and immunomodulatory roles place enteric glia in a unique position to regulate diverse gastrointestinal disease processes. In this Review, we discuss current concepts regarding enteric glial development, heterogeneity and functional roles in gastrointestinal pathophysiology and pathophysiology, with a focus on interactions with neurons and immune cells. We also present a working model to differentiate glial states based on normal function and disease-induced dysfunctions. Enteric glia regulate homeostasis in the enteric nervous system and influence gastrointestinal function. This Review provides an update on enteric glial biology and the underlying mechanisms by which enteric glia regulate gastrointestinal function and disease, with a focus on neuronal and immune interactions. Enteric glia are a heterogeneous population of peripheral neuroglia that regulate homeostasis in the enteric nervous system. Bidirectional communication between enteric glia and neurons modulates intestinal reflexes. Enteric glia are central players in neuroinflammation and contribute to neuroplasticity through interactions with neurons and immune cells. Enteric glia regulate disease processes involved in tumorigenesis and extragastrointestinal diseases. Therapies targeting glial mechanisms, such as gliotransmitter release or signalling pathways that promote gliosis, could substantially advance the treatment of common gastrointestinal diseases. Enteric glia are a heterogeneous population of peripheral neuroglia that regulate homeostasis in the enteric nervous system. Bidirectional communication between enteric glia and neurons modulates intestinal reflexes. Enteric glia are central players in neuroinflammation and contribute to neuroplasticity through interactions with neurons and immune cells. Enteric glia regulate disease processes involved in tumorigenesis and extragastrointestinal diseases. Therapies targeting glial mechanisms, such as gliotransmitter release or signalling pathways that promote gliosis, could substantially advance the treatment of common gastrointestinal diseases.
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Cited by
Aburto, M. R., & Cryan, J. F. (2024) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-023-00890-0 · Cited by 359
Toll-like receptor-mediated neuroinflammation: relevance for cognitive dysfunctions
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Role of the endocannabinoid system in the regulation of intestinal homeostasis
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Metadata
- Authors
- Seguella, L., & Gulbransen, B. D.
- Venue
- Nature Reviews Gastroenterology & Hepatology
- Published
- 2021-03-17
- Volume
- 18
- Issue
- 8
- Pages
- 571-587
- ISSN
- 1759-5045 (ISSN-L)
- 1759-5053
- OpenAlex
- W3137619127
- Cited by
- 323
- References
- 177
- FWCI
- 12.04
- Type
- journal article
- Language
- en
- Open access
- green
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- Seguella, L., & Gulbransen, B. D. (2021). Enteric glial biology, intercellular signalling and roles in gastrointestinal disease. Nature Reviews Gastroenterology & Hepatology. https://doi.org/10.1038/s41575-021-00423-7
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