Laboratory of Cell Biochemistry, Department of Biochemistry and Molecular Biology, Faculty of Medicine, University of Debrecen, Debrecen, 4032, Hungary.
Universitas Muhammadiyah Bangka Belitung, Pangkalpinang, 33134, Indonesia.
Sci Rep. 2024 Nov 16;14(1):28272. doi: 10.1038/s41598-024-79634-2.
Brown and beige adipocytes can be activated by β-adrenergic agonist via cAMP-dependent signaling. Performing RNA-sequencing analysis in human cervical area-derived adipocytes, we found that dibutyryl-cAMP, which can mimic in vivo stimulation of browning and thermogenesis, enhanced the expression of browning and batokine genes and upregulated several signaling pathway genes linked to thermogenesis. We observed that the expression of inhibitor of DNA binding and cell differentiation (ID) 1 and particularly ID3 was strongly induced by the adrenergic stimulation. The degradation of ID1 and ID3 elicited by the ID antagonist AGX51 during thermogenic activation prevented the induction of proton leak respiration that reflects thermogenesis and abrogated cAMP analogue-stimulated upregulation of thermogenic genes and mitochondrial complex I, II, and IV subunits, independently of the proximal cAMP-PKA signaling pathway. The presented data suggests that ID proteins contribute to efficient thermogenic response of adipocytes during adrenergic stimulation.
棕色和米色脂肪细胞可以通过β-肾上腺素能激动剂通过 cAMP 依赖性信号通路被激活。在人宫颈脂肪细胞中进行 RNA 测序分析,我们发现,二丁酰环腺苷酸(可模拟体内棕色化和产热的刺激)增强了棕色化和 batokine 基因的表达,并上调了几个与产热相关的信号通路基因。我们观察到,抑制 DNA 结合和细胞分化(ID)1 的表达,特别是 ID3,被肾上腺素刺激强烈诱导。在产热激活期间,ID 拮抗剂 AGX51 降解 ID1 和 ID3 可防止质子泄漏呼吸的诱导,该呼吸反映产热,并消除 cAMP 类似物刺激的产热基因和线粒体复合物 I、II 和 IV 亚基的上调,而不依赖于近端 cAMP-PKA 信号通路。所呈现的数据表明,ID 蛋白有助于脂肪细胞在肾上腺素刺激期间的有效产热反应。