4.5 Article

Enteric Glial Cells: A New Frontier in Neurogastroenterology and Clinical Target for Inflammatory Bowel Diseases

Journal

INFLAMMATORY BOWEL DISEASES
Volume 22, Issue 2, Pages 433-449

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1097/MIB.0000000000000667

Keywords

enteric glial cells; motility; tipartite synapse; calcium signaling; gliotransmission; neuroglial communication; inflammatory bowel diseases; GI infection; human enteric glial cell; postoperative ileus; enteric nervous system; reactive hEGC phenotype; purinergic signaling

Funding

  1. NINDS Diabetes and Kidney Diseases [DK093499]
  2. NCRR shared instrumentation Grant [S10RR11434]
  3. department of Anesthesiology and Neuroscience Signature Program at Wexner Medical Center
  4. Dr. R. Cuomo's group at the University of Naples, Italy
  5. Italian Ministry of University and Research, COFIN [2009HLNNRL]
  6. NIH Loan Repayment Program grant
  7. Davis Bremmer Foundation pre-K Award through NIH CTSA

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The word glia is derived from the Greek word , glue of the enteric nervous system, and for many years, enteric glial cells (EGCs) were believed to provide mainly structural support. However, EGCs as astrocytes in the central nervous system may serve a much more vital and active role in the enteric nervous system, and in homeostatic regulation of gastrointestinal functions. The emphasis of this review will be on emerging concepts supported by basic, translational, and/or clinical studies, implicating EGCs in neuron-to-glial (neuroglial) communication, motility, interactions with other cells in the gut microenvironment, infection, and inflammatory bowel diseases. The concept of the reactive glial phenotype is explored as it relates to inflammatory bowel diseases, bacterial and viral infections, postoperative ileus, functional gastrointestinal disorders, and motility disorders. The main theme of this review is that EGCs are emerging as a new frontier in neurogastroenterology and a potential therapeutic target. New technological innovations in neuroimaging techniques are facilitating progress in the field, and an update is provided on exciting new translational studies. Gaps in our knowledge are discussed for further research. Restoring normal EGC function may prove to be an efficient strategy to dampen inflammation. Probiotics, palmitoylethanolamide (peroxisome proliferator-activated receptor-), interleukin-1 antagonists (anakinra), and interventions acting on nitric oxide, receptor for advanced glycation end products, S100B, or purinergic signaling pathways are relevant clinical targets on EGCs with therapeutic potential.

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