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对人脂肪细胞进行慢性肿瘤坏死因子α(TNFalpha)和环磷酸腺苷(cAMP)预处理可改变激素敏感性脂肪酶(HSL)、脂肪甘油三酯脂肪酶(ATGL)和 perilipin,从而调节基础和刺激后的脂肪分解。

Chronic TNFalpha and cAMP pre-treatment of human adipocytes alter HSL, ATGL and perilipin to regulate basal and stimulated lipolysis.

作者信息

Bézaire Véronic, Mairal Aline, Anesia Rodica, Lefort Corinne, Langin Dominique

机构信息

Laboratoire de Recherches sur Obésités, Inserm U858, Toulouse, France.

出版信息

FEBS Lett. 2009 Sep 17;583(18):3045-9. doi: 10.1016/j.febslet.2009.08.019. Epub 2009 Aug 18.

Abstract

We examined the effects of chronic TNFalpha and dibutyryl-cAMP (Db-cAMP) pre-treatment on the lipolytic machinery of human hMADS adipocytes. TNFalpha decreased adipose triglyceride lipase (ATGL) and hormone-sensitive lipase (HSL) protein content and triglycerides (TG)-hydrolase activity but increased basal lipolysis due to a marked reduction in perilipin (PLIN) protein content. Conversely, Db-cAMP increased ATGL and HSL protein content but prevented PLIN phosphorylation, the net result being accentuated basal lipolysis. In forskolin-stimulated conditions, TNFalpha and Db-cAMP pre-treatment decreased stimulated TG-hydrolase activity and impaired PLIN phosphorylation. Together, this resulted in a severely attenuated response to forskolin-stimulated lipolysis.

摘要

我们研究了慢性肿瘤坏死因子α(TNFα)和二丁酰环磷腺苷(Db-cAMP)预处理对人hMADS脂肪细胞脂解机制的影响。TNFα降低了脂肪甘油三酯脂肪酶(ATGL)和激素敏感性脂肪酶(HSL)的蛋白质含量以及甘油三酯(TG)水解酶活性,但由于围脂滴蛋白(PLIN)蛋白质含量显著降低,基础脂解增加。相反,Db-cAMP增加了ATGL和HSL的蛋白质含量,但阻止了PLIN磷酸化,最终结果是基础脂解增强。在福斯高林刺激的条件下,TNFα和Db-cAMP预处理降低了刺激后的TG水解酶活性,并损害了PLIN磷酸化。这些共同导致对福斯高林刺激的脂解反应严重减弱。

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