Aberrant Deactivation-Induced Gain of Function in TRPM4 Mutant Is Associated with Human Cardiac Conduction Block

Xian W, Hui X, Tian Q, Wang H, Moretti A, Laugwitz KL, Flockerzi V, Ruppenthal S, Lipp P (2018)

Publication Type: Journal article

Publication year: 2018

Journal

Cell Reports Elsevier (Cell Press)

Book Volume: 24

Pages Range: 724-731

Journal Issue: 3

DOI: 10.1016/j.celrep.2018.06.034

Abstract

A gain-of-function mutation in the Ca²⁺-activated transient receptor potential melastatin member 4 (TRPM4^A432T) is linked to life-threatening cardiac conduction disturbance, but the underlying mechanism is unclear. For deeper insights, we used photolysis of caged Ca²⁺, quantitative Ca²⁺, and electrophysiological measurements. TRPM4^A432T’s 2-fold larger membrane current was associated with 50% decreased plasma membrane expression. Kinetic analysis unveiled 4-fold slower deactivation that was responsible for the augmented membrane current progressively rising during repetitive human cardiac action potentials. Rational mutagenesis of TRPM4 at position 432 revealed that the bulkiness of the amino acid was key to TRPM4^A432T’s aberrant gating. Charged amino acids rendered the channel non-functional. The slow deactivation caused by an amino acid substitution at position 432 from alanine to the bulkier threonine represents a key contributor to the gain of function in TRPM4^A432T. Thus, our results add a mechanism in the etiology of TRP channel-linked human cardiac channelopathies. A mutation in TRPM4 (A432T) is linked to life-threatening cardiac conduction disturbances in patients. Using a combination of biophysical techniques, Xian et al. demonstrate that calcium-dependent deactivation between heartbeats is aberrant and highlights the etiology of human cardiac channelopathies. These findings offer putative new pharmacological targets for disease management in human patients.

Involved external institutions

Universität des Saarlandes (UdS)

Germany (DE) Technische Universität München (TUM)

Germany (DE)

How to cite

APA:

Xian, W., Hui, X., Tian, Q., Wang, H., Moretti, A., Laugwitz, K.-L.,... Lipp, P. (2018). Aberrant Deactivation-Induced Gain of Function in TRPM4 Mutant Is Associated with Human Cardiac Conduction Block. Cell Reports, 24(3), 724-731. https://doi.org/10.1016/j.celrep.2018.06.034

MLA:

Xian, Wenying, et al. "Aberrant Deactivation-Induced Gain of Function in TRPM4 Mutant Is Associated with Human Cardiac Conduction Block." Cell Reports 24.3 (2018): 724-731.

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