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Cytoskeleton社 Neuropathy-causing TRPV4 mutations disrupt TRPV4-RhoA interactions

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Neuropathy-causing_TRPV4_mutations_disrupt_TRPV4-RhoA_interactions_1.jpgNeuropathy-causing TRPV4 mutations disrupt TRPV4-RhoA interactions

Transient receptor potential vanilloid 4 (TRPV4) is a homotetrameric ion channel that coordinates a variety of cellular processes in response to extracellular environmental stimuli. Interestingly, mutations in TRPV4 result in an array of pathologies such as neuropathy and skeletal dysplasia; nonetheless, the cause of these diseases appears to have a common underlying factor, that is, a dysfunction in cytoskeletal processes. Recently, McCray et al. sought to understand the mechanisms by which TRPV4-mutations alter cytoskeletal function and neuropathy.  ... 

 

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Neuropathy-causing_TRPV4_mutations_disrupt_TRPV4-RhoA_interactions_2.gifAbove: Schematic for TRPV4–RhoA functional interactions. Inactive TRPV4 channels bind GDP-bound RhoA. Activation of TRPV4 ion channel leads to release of RhoA, calcium-dependent RhoA activation, and enhanced cytoskeletal changes.

Link to Citation:

 

McCray B. et al. Neuropathy-causing TRPV4 mutations disrupt TRPV4-RhoA interactions and impair neurite extension. Nat Commun. 2021 Mar 4;12(1):1444. doi: 10.1038/s41467-021-21699-y.

 

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