PIEZO2 ion channels in proprioception.

Curr Opin Neurobiol

Sensory Cells and Circuits Section, National Center for Complementary and Integrative Health, 35 Convent Drive, Bethesda, MD, 20892, USA. Electronic address:

Published: August 2022

AI Article Synopsis

  • PIEZO2 is a crucial ion channel in somatosensory neurons, and mutations in its gene lead to significant mechanosensory issues, including loss of proprioception in humans.
  • Studies on both humans with PIEZO2 mutations and knockout mouse models reveal the gene's essential role in detecting mechanical stimuli, affecting everyday activities.
  • Recent discoveries emphasize the complexity of proprioceptors and their functions, paving the way for better understanding of how our body senses and responds to mechanical input to enhance posture and motor control.

Article Abstract

PIEZO2 is a stretch-gated ion channel that is expressed at high levels in somatosensory neurons. Humans with rare mutations in the PIEZO2 gene have profound mechanosensory deficits that include a loss of the sense of proprioception. These striking phenotypes match those seen in conditional knockout mouse models demonstrating the highly conserved function for this gene. Here, we review the ramifications of loss of PIEZO2 function on normal daily activities and what studies like these have revealed about proprioception at the molecular and cellular level. Additionally, we highlight recent work that has uncovered the surprising functional and molecular diversity of proprioceptors. Together, these findings pioneer a path toward determining how the detection of mechanosensory input from muscles and tendons is used to control posture and refine motor performance.

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Source
http://dx.doi.org/10.1016/j.conb.2022.102572DOI Listing

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