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脂联素与儿茶酚胺的串扰。

The crosstalks between adipokines and catecholamines.

机构信息

Division of Bioengineering, Nanyang Technological University, 70 Nanyang Drive, Singapore 637457, Singapore.

出版信息

Mol Cell Endocrinol. 2011 Jan 30;332(1-2):261-70. doi: 10.1016/j.mce.2010.11.002. Epub 2010 Nov 9.

Abstract

Adipocytes, which secrete a spectrum of adipokines, play an integral role in metabolism via communications with other endocrine cells. In the present work, we have studied the interplays between adipokines and catecholamines, using 3T3-L1 adipocytes and PC12 cells as the cell models and an integrative experimental platform. We demonstrate that all catecholamines inhibit vesicle trafficking and secretion of leptin and resistin through β-adrenergic receptors, while leptin and resistin enhance the vesicle trafficking and secretion of catecholamines through PKC, PKA, MAPK kinase and Ca(2+) dependent pathways. The crosstalks between adipokines and catecholamines were further corroborated by co-culturing 3T3-L1 adipocytes and PC12 cells. Our findings highlight the importance of adipo-adrenal axis in energy metabolism and the intricate interactions between metabolic hormones.

摘要

脂肪细胞通过与其他内分泌细胞的通讯,分泌一系列脂肪因子,在代谢中发挥着重要作用。在本工作中,我们使用 3T3-L1 脂肪细胞和 PC12 细胞作为细胞模型,并采用综合实验平台,研究了脂肪因子和儿茶酚胺之间的相互作用。我们证明,所有儿茶酚胺均通过β-肾上腺素能受体抑制瘦素和抵抗素的囊泡运输和分泌,而瘦素和抵抗素则通过 PKC、PKA、MAPK 激酶和 Ca(2+)依赖途径增强儿茶酚胺的囊泡运输和分泌。脂肪因子和儿茶酚胺之间的串扰进一步通过共培养 3T3-L1 脂肪细胞和 PC12 细胞得到证实。我们的研究结果强调了脂肪-肾上腺轴在能量代谢中的重要性以及代谢激素之间错综复杂的相互作用。

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