Loss of endothelial TRPC1 aggravates metabolic dysfunction in obesity via disrupting adipose tissue homeostasis

This study, for the first time, elucidates the pivotal role of endothelial TRPC1 in maintaining metabolic homeostasis by orchestrating an "inflammation-thermogenesis-metabolite" regulatory network. Specifically, the deficiency of endothelial TRPC1 exacerbates metabolic dysfunction associated with obesity, whereas its overexpression exerts significant protective effects. These findings highlight the centrality of endothelial ion channels in vascular-metabolic coupling, thereby establishing a theoretical rationale for targeting TRPC1 as a therapeutic strategy against metabolic syndrome.

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Publication Details

Journal
Frontiers in Molecular Biosciences
Published
2025-06-11
DOI
https://doi.org/10.3389/fmolb.2025.1619559
Citations
1
Primary Topic
Adipose Tissue and Metabolism
Type
article
Field-Weighted Citation Impact
1.16
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article

Loss of endothelial TRPC1 aggravates metabolic dysfunction in obesity via disrupting adipose tissue homeostasis

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Frontiers in Molecular Biosciences
Adipose Tissue and Metabolism
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article

Loss of endothelial TRPC1 aggravates metabolic dysfunction in obesity via disrupting adipose tissue homeostasis

Yifei Zhu, Yingxia Lan, Yuan Chu, Shiquan Wang, Lei Feng, Yizhi Zhang, Yu Fan, Yuan Liu
article en
1 citations

Abstract

This study, for the first time, elucidates the pivotal role of endothelial TRPC1 in maintaining metabolic homeostasis by orchestrating an "inflammation-thermogenesis-metabolite" regulatory network. Specifically, the deficiency of endothelial TRPC1 exacerbates metabolic dysfunction associated with obesity, whereas its overexpression exerts significant protective effects. These findings highlight the centrality of endothelial ion channels in vascular-metabolic coupling, thereby establishing a theoretical rationale for targeting TRPC1 as a therapeutic strategy against metabolic syndrome.

Frontiers in Molecular BiosciencesVol. 12
Jiangnan University (CN)
Openalex Percentile: Top 21%
Adipose Tissue and Metabolism
1.16
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