Identification of a human mitochondrial isoform of TRPV1: a thermostat regulating mitochondrial maximal temperature?

Abstract Mitochondria are well known to produce ATP for cell energy requirements and thermogenesis simultaneously by the respiratory chain, with a potential optimum temperature of 50 °C, while deleterious overheating should be prevented by a yet unknown system. Here, we report the identification of a human Transient Receptor Potential Vanilloid 1 (mitoTRPV1) alternative isoform located in the mitochondrial inner membrane, which acts as a thermostat regulating mitochondrial maximal temperature. The ubiquitously expressed mitoTRPV1 open reading frame overlaps TRPV1 exons 1 and 2 and intron 2 in a + 1 frame, encoding for an effective 150 amino-acid N-terminal mitochondrial targeting sequence (MTS) conserved amongst mammalian species, followed by the 687 amino acids of the TRPV1 C-terminal sequence. Pharmacological activation of mitoTRPV1 induces a low cytoplasmic Ca 2+ increase and mitochondrial cooling without modification of mitochondrial respiration and ATP production. We conclude that, in our experimental conditions, mitoTRPV1 acts as a thermostat to promote mitochondrial thermolysis without impairing respiration and ATP production. They point to the potential implication of mitoTRPV1 in human diseases related to temperature dysregulation, and should be further studied in physiological conditions in cellular and animal models expressing mitoTRPV1 endogenously.

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Publication Details

Journal
Cellular and Molecular Life Sciences
Published
2026-07-23
DOI
https://doi.org/10.1007/s00018-026-06360-5
Primary Topic
Adipose Tissue and Metabolism
Type
article
Field-Weighted Citation Impact
0.00

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article

Identification of a human mitochondrial isoform of TRPV1: a thermostat regulating mitochondrial maximal temperature?

Sylvie Ducreux, Salim Khiati, Florian Beignon, Artur Wardaszka et al.
Cellular and Molecular Life Sciences
Adipose Tissue and Metabolism
article

Identification of a human mitochondrial isoform of TRPV1: a thermostat regulating mitochondrial maximal temperature?

Sylvie Ducreux, Salim Khiati, Florian Beignon, Artur Wardaszka, Naïg Guéguen, Méline Wery, César Mattei, Yannick Le Dantec, Adélie Mellinger, Caroline Bosson, Florentin Moulin, David Goudenège, Arnaud Chevrollier, Morgane Lemao, Hélène Tricoire-Leignel, Guy Lenaers, Léa Tuifua, Nathalie Roux-Buisson, J Faure, Piotr Bednarczyk, Lucie Maujean, Camille Blaecke, Joanna K. Bujak
article en

Abstract

Abstract Mitochondria are well known to produce ATP for cell energy requirements and thermogenesis simultaneously by the respiratory chain, with a potential optimum temperature of 50 °C, while deleterious overheating should be prevented by a yet unknown system. Here, we report the identification of a human Transient Receptor Potential Vanilloid 1 (mitoTRPV1) alternative isoform located in the mitochondrial inner membrane, which acts as a thermostat regulating mitochondrial maximal temperature. The ubiquitously expressed mitoTRPV1 open reading frame overlaps TRPV1 exons 1 and 2 and intron 2 in a + 1 frame, encoding for an effective 150 amino-acid N-terminal mitochondrial targeting sequence (MTS) conserved amongst mammalian species, followed by the 687 amino acids of the TRPV1 C-terminal sequence. Pharmacological activation of mitoTRPV1 induces a low cytoplasmic Ca 2+ increase and mitochondrial cooling without modification of mitochondrial respiration and ATP production. We conclude that, in our experimental conditions, mitoTRPV1 acts as a thermostat to promote mitochondrial thermolysis without impairing respiration and ATP production. They point to the potential implication of mitoTRPV1 in human diseases related to temperature dysregulation, and should be further studied in physiological conditions in cellular and animal models expressing mitoTRPV1 endogenously.

Cellular and Molecular Life Sciences
Université Claude Bernard Lyon 1 (FR), Centre National de la Recherche Scientifique (FR), Inserm (FR), Warsaw University of Life Sciences (PL), Centre Hospitalier Universitaire de Grenoble (FR), Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement (FR), Centre Hospitalier Universitaire d'Angers (FR), Laboratoire de recherche en cardiovasculaire, métabolisme, diabétologie et nutrition (FR), Grenoble Institute of Neurosciences (FR), Université d'Angers (FR), Université Grenoble Alpes (FR)
Agence Nationale de la Recherche, Institut National de la Santé et de la Recherche Médicale, Narodowe Centrum Nauki, Délégation Générale pour l'Armement, Université Claude Bernard Lyon 1, Universite Angers, Conseil Régional des Pays de la Loire
Affordable and clean energy
Openalex Percentile: Top 9%
Adipose Tissue and Metabolism
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