TY - JOUR
T1 - Enteric Glial Cells
T2 - A New Frontier in Neurogastroenterology and Clinical Target for Inflammatory Bowel Diseases
AU - Ochoa-Cortes, Fernando
AU - Turco, Fabio
AU - Linan-Rico, Andromeda
AU - Soghomonyan, Suren
AU - Whitaker, Emmett
AU - Wehner, Sven
AU - Cuomo, Rosario
AU - Christofi, Fievos L.
N1 - Publisher Copyright:
© 2016 Crohn's & Colitis Foundation of America, Inc.
PY - 2016/1/11
Y1 - 2016/1/11
N2 - The word glia is derived from the Greek word για, 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-α), 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.
AB - The word glia is derived from the Greek word για, 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-α), 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.
KW - GI infection
KW - calcium signaling
KW - enteric glial cells
KW - enteric nervous system
KW - gliotransmission
KW - human enteric glial cell
KW - inflammatory bowel diseases
KW - motility
KW - neuroglial communication
KW - postoperative ileus
KW - purinergic signaling
KW - reactive hEGC phenotype
KW - tipartite synapse
UR - http://www.scopus.com/inward/record.url?scp=84955580382&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84955580382&partnerID=8YFLogxK
U2 - 10.1097/MIB.0000000000000667
DO - 10.1097/MIB.0000000000000667
M3 - Article
C2 - 26689598
AN - SCOPUS:84955580382
SN - 1078-0998
VL - 22
SP - 433
EP - 449
JO - Inflammatory bowel diseases
JF - Inflammatory bowel diseases
IS - 2
ER -