TY - JOUR
T1 - Mechanosensing in Metabolism
AU - Tranter, John D.
AU - Kumar, Ashutosh
AU - Nair, Vinayak K.
AU - Sah, Rajan
N1 - Publisher Copyright:
© American Physiological Society.
PY - 2024/1
Y1 - 2024/1
N2 - Electrical mechanosensing is a process mediated by specialized ion channels, gated directly or indirectly by mechanical forces, which allows cells to detect and subsequently respond to mechanical stimuli. The activation of mechanosensitive (MS) ion channels, intrinsically gated by mechanical forces, or mechanoresponsive (MR) ion channels, indirectly gated by mechanical forces, results in electrical signaling across lipid bilayers, such as the plasma membrane. While the functions of mechanically gated channels within a sensory context (e.g., proprioception and touch) are well described, there is emerging data demonstrating functions beyond touch and proprioception, including mechanoregulation of intracellular signaling and cellular/systemic metabolism. Both MR and MS ion channel signaling have been shown to contribute to the regulation of metabolic dys-function, including obesity, insulin resistance, impaired insulin secretion, and inflammation. This review summarizes our current understanding of the contributions of several MS/MR ion channels in cell types implicated in metabolic dysfunction, namely, adipocytes, pancreatic β-cells, hepa-tocytes, and skeletal muscle cells, and discusses MS/MR ion channels as possible therapeutic targets.
AB - Electrical mechanosensing is a process mediated by specialized ion channels, gated directly or indirectly by mechanical forces, which allows cells to detect and subsequently respond to mechanical stimuli. The activation of mechanosensitive (MS) ion channels, intrinsically gated by mechanical forces, or mechanoresponsive (MR) ion channels, indirectly gated by mechanical forces, results in electrical signaling across lipid bilayers, such as the plasma membrane. While the functions of mechanically gated channels within a sensory context (e.g., proprioception and touch) are well described, there is emerging data demonstrating functions beyond touch and proprioception, including mechanoregulation of intracellular signaling and cellular/systemic metabolism. Both MR and MS ion channel signaling have been shown to contribute to the regulation of metabolic dys-function, including obesity, insulin resistance, impaired insulin secretion, and inflammation. This review summarizes our current understanding of the contributions of several MS/MR ion channels in cell types implicated in metabolic dysfunction, namely, adipocytes, pancreatic β-cells, hepa-tocytes, and skeletal muscle cells, and discusses MS/MR ion channels as possible therapeutic targets.
UR - http://www.scopus.com/inward/record.url?scp=85181414736&partnerID=8YFLogxK
U2 - 10.1002/cphy.c230005
DO - 10.1002/cphy.c230005
M3 - Article
C2 - 38158369
AN - SCOPUS:85181414736
SN - 2040-4603
VL - 14
SP - 5269
EP - 5290
JO - Comprehensive Physiology
JF - Comprehensive Physiology
IS - 1
ER -