TRPM4 inhibition slows neuritogenesis progression of cortical neurons

TRPM4 is a non-selective cation channel activated by intracellular Ca<sup>2+</sup> but only permeable to monovalent cations, its activation regulates membrane potential and intracellular calcium. This channel participates in the migration and adhesion of non-excitable cells and forms an integral part of the focal adhesion complex. In neurons, TRPM4 expression starts before birth and its function at this stage is not clear, but it may function in processes such as neurite development. Here we investigate the role of TRPM4 in neuritogenesis. We found that neurons at DIV 0 express TRPM4, the inhibition of TRPM4 using 9-Ph reduces neurite number and slows the progression of neurite development, keeping neurons in stage 1. The genetic suppression of TRPM4 using an shRNA at later stages (DIV2) reduces neurite length. Conversely, at DIV 0, TRPM4 inhibition augments the Cch-induced Ca<sup>2 +</sup> <sub>i</sub> increase, altering the calcium homeostasis. Together, these results show that TRPM4 participates in progression of neurite development and suggest a critical role of the calcium modulation during this stage of neuronal development.

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Publication Details

Journal
Molecular Brain
Published
2024-09-12
DOI
https://doi.org/10.1186/s13041-024-01140-3
Citations
2
Primary Topic
Ion Channels and Receptors
Type
article
Field-Weighted Citation Impact
0.72

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article

TRPM4 inhibition slows neuritogenesis progression of cortical neurons

Elías Leiva‐Salcedo, D. Riquelme, Nicole Juanchuto-Viertel, Carlos Álamos
2 citations
Molecular Brain
Ion Channels and Receptors
0.72
article

TRPM4 inhibition slows neuritogenesis progression of cortical neurons

Elías Leiva‐Salcedo, D. Riquelme, Nicole Juanchuto-Viertel, Carlos Álamos
article en
2 citations

Abstract

TRPM4 is a non-selective cation channel activated by intracellular Ca<sup>2+</sup> but only permeable to monovalent cations, its activation regulates membrane potential and intracellular calcium. This channel participates in the migration and adhesion of non-excitable cells and forms an integral part of the focal adhesion complex. In neurons, TRPM4 expression starts before birth and its function at this stage is not clear, but it may function in processes such as neurite development. Here we investigate the role of TRPM4 in neuritogenesis. We found that neurons at DIV 0 express TRPM4, the inhibition of TRPM4 using 9-Ph reduces neurite number and slows the progression of neurite development, keeping neurons in stage 1. The genetic suppression of TRPM4 using an shRNA at later stages (DIV2) reduces neurite length. Conversely, at DIV 0, TRPM4 inhibition augments the Cch-induced Ca<sup>2 +</sup> <sub>i</sub> increase, altering the calcium homeostasis. Together, these results show that TRPM4 participates in progression of neurite development and suggest a critical role of the calcium modulation during this stage of neuronal development.

Molecular BrainVol. 17(1)
Universidad de Santiago de Chile (CL), University of Chile (CL)
Universidad de Santiago de Chile, Agencia Nacional de Investigación y Desarrollo, Departamento de Investigaciones Científicas y Tecnológicas, Universidad de Santiago de Chile
Openalex Percentile: Top 31%
Ion Channels and Receptors
0.72
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