Suppr超能文献

嘌呤能受体P2X5调节棕色脂肪组织中的葡萄糖代谢和产热基因表达。

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

作者信息

Jaeckstein Michelle Y, Miegel Lisa, Behrens Janina, Stähler Tobias, Diercks Björn-Philipp, Heine Markus, Koch-Nolte Friedrich, Heeren Joerg

机构信息

Department of Biochemistry and Molecular Cell Biology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.

Institute of Immunology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.

出版信息

Int J Mol Sci. 2025 Jul 4;26(13):6474. doi: 10.3390/ijms26136474.

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.

摘要

除了肾上腺素能信号传导外,由细胞外腺嘌呤核苷酸介导的嘌呤能途径已被描述为可调节棕色脂肪组织(BAT)的产热和代谢功能。在此,我们描述了P2X5在BAT成熟脂肪细胞和体外分化的棕色脂肪细胞中被ATP激活后的高表达。其他P2X家族成员的水平则低得多,或者其表达仅限于组织驻留巨噬细胞或内皮细胞。全身性和棕色脂肪细胞特异性的P2rx5缺陷导致解偶联蛋白1(UCP1)的表达降低。然而,间接量热法研究表明,P2X5并不影响全身能量消耗。值得注意的是,在正常饮食和致肥胖的高脂肪饮食条件下,葡萄糖耐量均受损,这可以通过BAT而非其他器官中葡萄糖处理减少来解释。总之,这些数据表明P2X5在全身和BAT特异性葡萄糖代谢中具有调节作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8b9/12249994/db30a2b80948/ijms-26-06474-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验