The emerging roles of piezo1 channels in animal models of multiple sclerosis

Abstract

Multiple sclerosis (MS) is a chronic inflammatory, demyelinating, and neurodegenerative disease in the central nervous system (CNS). Its pathogenesis is quite complex: Accumulated evidence suggests that biochemical signals as well as mechanical stimuli play important roles in MS. In both patients and animal models of MS, brain viscoelasticity is reduced during disease progression. Piezo mechanosensitive channels are recently discovered, and their three-dimensional structure has been solved. Both the membrane dome mechanism and the membrane footprint hypothesis have been proposed to explain their mechanosensitivity. While membrane-mediated forces alone appear to be sufficient to induce Piezo gating, tethers attached to the membrane or to the channel itself also seem to play a role. Current research indicates that Piezo1 channels play a key role in multiple aspects of MS pathogenesis. Activation of Piezo1 channels in axon negatively regulates CNS myelination. in addition, the inhibition of Piezo1 in CD4+ T cells and/or T regulatory cells (Treg) attenuates experimental autoimmune encephalitis (EAE) symptoms. Although more work has to be done to clarify the roles of Piezo1 channels in MS, they might be a promising future drug target for MS treatment.

Roles of TRP and PIEZO receptors in autoimmune diseases

“…PIEZO1 depletion in T cells can selectively promote regulatory T-cell proliferation, thereby reducing EAE severity. However, it does not affect thymus development, lymph node homing, T-cell receptor priming, T-cell proliferation and differentiation (Refs 142, 143).…”

Mechanobiological insight into brain diseases based on mechanosensitive channels: Common mechanisms and clinical potential

“…The cerebral softening is also observed in patients with multiple sclerosis, another neurodegenerative disease featuring progressively demyelinating. 106 The stiffness of the brain is a potential biomarker for reporting multiple sclerosis. 95 …”