The Purinergic Receptor P2X5 Modulates Glucose Metabolism and Expression of Thermogenic Genes in Brown Adipose Tissue

Next to adrenergic signalling, purinergic pathways mediated by extracellular adenine nucleotides have been described to shape thermogenic and metabolic functions in brown adipose tissue (BAT). Here we describe high expression of P2X5 that is activated by ATP in mature adipocytes of BAT and differentiated brown adipocytes in vitro. The levels of other P2X family members were much lower, or expression was restricted to tissue-resident macrophages or endothelial cells. Global and brown adipocyte-specific P2rx5 deficiency resulted in lower expression of the uncoupling protein 1 (UCP1). However, indirect calorimetry studies showed that P2X5 did not affect systemic energy expenditure. Of note, glucose tolerance was impaired under chow and obesogenic high-fat diet conditions, which can be explained by lower glucose disposal into BAT but not into other organs. In summary, these data indicate a modulatory role of P2X5 in systemic and BAT-specific glucose metabolism.

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Publication Details

Journal
International Journal of Molecular Sciences
Published
2025-07-04
DOI
https://doi.org/10.3390/ijms26136474
Citations
1
Primary Topic
Adipose Tissue and Metabolism
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article
Field-Weighted Citation Impact
1.16
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article

The Purinergic Receptor P2X5 Modulates Glucose Metabolism and Expression of Thermogenic Genes in Brown Adipose Tissue

Jöerg Heeren, Michelle Y. Jaeckstein, Björn‐Philipp Diercks, Janina Behrens et al.
1 citations
International Journal of Molecular Sciences
Adipose Tissue and Metabolism
1.16
article

The Purinergic Receptor P2X5 Modulates Glucose Metabolism and Expression of Thermogenic Genes in Brown Adipose Tissue

Jöerg Heeren, Michelle Y. Jaeckstein, Björn‐Philipp Diercks, Janina Behrens, Friedrich Koch‐Nolte, Markus Heine, Tobias Stähler, Lisa Miegel
article en
1 citations

Abstract

Next to adrenergic signalling, purinergic pathways mediated by extracellular adenine nucleotides have been described to shape thermogenic and metabolic functions in brown adipose tissue (BAT). Here we describe high expression of P2X5 that is activated by ATP in mature adipocytes of BAT and differentiated brown adipocytes in vitro. The levels of other P2X family members were much lower, or expression was restricted to tissue-resident macrophages or endothelial cells. Global and brown adipocyte-specific P2rx5 deficiency resulted in lower expression of the uncoupling protein 1 (UCP1). However, indirect calorimetry studies showed that P2X5 did not affect systemic energy expenditure. Of note, glucose tolerance was impaired under chow and obesogenic high-fat diet conditions, which can be explained by lower glucose disposal into BAT but not into other organs. In summary, these data indicate a modulatory role of P2X5 in systemic and BAT-specific glucose metabolism.

International Journal of Molecular SciencesVol. 26(13)
Universität Hamburg (DE), University Medical Center Hamburg-Eppendorf (DE)
Openalex Percentile: Top 20%
Adipose Tissue and Metabolism
1.16
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