MDFIC2 is a sensory neuron–specific PIEZO channel auxiliary subunit

Z Zijing Zhou (Molecular Cardiology and Biophysics, Victor Chang Cardiac Research Institute) F Fei Dai (Interdisciplinary Research Center on Biology and Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences) D Delfine Cheng (Molecular Cardiology and Biophysics, Victor Chang Cardiac Research Institute) X Xiaonuo Ma (Interdisciplinary Research Center on Biology and Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences) S Seyedeh Farzaneh Omidkhoda (Molecular Cardiology and Biophysics, Victor Chang Cardiac Research Institute) J Jack Clarke (Molecular Cardiology and Biophysics, Victor Chang Cardiac Research Institute) H Huijing Zhang (Interdisciplinary Research Center on Biology and Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences) M Michael Laden (Molecular Cardiology and Biophysics, Victor Chang Cardiac Research Institute) Y Yang Guo (Department of Materials Science and Engineering, City University of Hong Kong, 83 Tat Chee Avenue, Kowloon 999077, Hong Kong SAR, China) J Jinyuan Vero Li (Molecular Cardiology and Biophysics, Victor Chang Cardiac Research Institute) R Renjing Liu (Molecular Cardiology and Biophysics, Victor Chang Cardiac Research Institute) E Emily S. Wong Y Yixiao Zhang C Charles D. Cox (Molecular Cardiology and Biophysics, Victor Chang Cardiac Research Institute)

Abstract

PIEZO channels are critical for sensory mechanotransduction. While MyoD-family inhibitor proteins were identified as PIEZO1 auxiliary subunits, their broader regulatory roles, particularly in sensory cells, remained unclear. Here, we demonstrate native MDFIC and MDFI regulate endogenous PIEZO channel currents in various nonsensory cell types. However, neither MDFIC nor MDFI are expressed in primary sensory neurons. In these cell types, we identified an uncharacterized third member of this family, Mdfic2 / Gm765 , that shares the ability to physically bind to PIEZO1 and PIEZO2. MDFIC2 is selectively expressed in subsets of mechanosensitive neurons, including dorsal root ganglia, trigeminal ganglia, and vagal sensory neurons. Like its paralogues, MDFIC2 alters PIEZO1/2 mechanosensitivity and inactivation kinetics, converting them into high-threshold slowly inactivating mechanoreceptors. Extensive cryo-EM reveals a conserved binding pocket for these auxiliary subunits in the pore modules of both PIEZO1 and PIEZO2 mediated by the posttranslationally modified distal C termini of MyoD-family inhibitor proteins. This structural and functional characterization of MyoD-family inhibitor proteins as PIEZO1/2 channel auxiliary subunits offers insights into the mechanobiology of nonsensory and sensory cells.

Article Details

Volume / Issue Vol. 123, Issue 15
Published April 14, 2026
ISSN 0027-8424
Publisher National Academy of Sciences

Authors (14)

Z

Zijing Zhou

Molecular Cardiology and Biophysics, Victor Chang Cardiac Research Institute

F

Fei Dai

Interdisciplinary Research Center on Biology and Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences

D

Delfine Cheng

Molecular Cardiology and Biophysics, Victor Chang Cardiac Research Institute

X

Xiaonuo Ma

Interdisciplinary Research Center on Biology and Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences

S

Seyedeh Farzaneh Omidkhoda

Molecular Cardiology and Biophysics, Victor Chang Cardiac Research Institute

J

Jack Clarke

Molecular Cardiology and Biophysics, Victor Chang Cardiac Research Institute

H

Huijing Zhang

Interdisciplinary Research Center on Biology and Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences

M

Michael Laden

Molecular Cardiology and Biophysics, Victor Chang Cardiac Research Institute

Y

Yang Guo

Department of Materials Science and Engineering, City University of Hong Kong, 83 Tat Chee Avenue, Kowloon 999077, Hong Kong SAR, China

J

Jinyuan Vero Li

Molecular Cardiology and Biophysics, Victor Chang Cardiac Research Institute

R

Renjing Liu

Molecular Cardiology and Biophysics, Victor Chang Cardiac Research Institute

E

Emily S. Wong

Y

Yixiao Zhang

C

Charles D. Cox

Molecular Cardiology and Biophysics, Victor Chang Cardiac Research Institute