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肿瘤坏死因子可提高脂肪细胞原代培养物中的脂肪分解速率,而不会改变激素敏感性脂肪酶的水平。

Tumor necrosis factor increases the rate of lipolysis in primary cultures of adipocytes without altering levels of hormone-sensitive lipase.

作者信息

Green A, Dobias S B, Walters D J, Brasier A R

机构信息

Department of Internal Medicine, University of Texas Medical Branch, Galveston 77555.

出版信息

Endocrinology. 1994 Jun;134(6):2581-8. doi: 10.1210/endo.134.6.8194485.

Abstract

To investigate the effects of cytokines on adipocyte lipolysis, a macrophage cell line (RAW 264.7) was treated with Escherichia coli lipopolysaccharide (1 microgram/ml) for 18 h to induce cytokine release. Conditioned medium (5%, vol/vol) from these cells was added to rat epididymal adipocytes isolated and incubated under sterile conditions. After incubation, the adipocytes were washed, and the rate of lipolysis (glycerol release) was determined after a further 1-h incubation. The conditioned medium caused an approximately 2.7-fold increase in lipolysis, detectable after 6-12 h, maximal by 24 h, and reversible by 48 h after washing the cells. The effect of conditioned medium was reversed by a neutralizing antibody to mouse tumor necrosis factor-alpha (TNF alpha), and the direct addition of recombinant human TNF alpha (0.1-50 ng/ml) reproduced the effect, with a half-maximally effective concentration of approximately 3 ng/ml. The effect of TNF on the expression of hormone-sensitive lipase (HSL; the rate-limiting enzyme for lipolysis) was investigated by Western immunoblots using an antibody raised to a bacterially expressed 96-amino acid portion of the HSL enzyme. TNF treatment did not alter the concentration of immunoreactive HSL. From these data we conclude that 1) macrophages release a cytokine(s) in response to lipopolysaccharide that stimulates lipolysis in freshly isolated adipocytes; 2) TNF alpha can account for most, or perhaps all, of this effect; 3) TNF alpha increases the rate of lipolysis by a mechanism that does not involve increased expression of HSL. Based on the time-dependent aspects of TNF alpha stimulation and the lack of change in immunoreactive HSL, the findings suggest a TNF-induced posttranslational modification of the enzyme.

摘要

为研究细胞因子对脂肪细胞脂解作用的影响,用大肠杆菌脂多糖(1微克/毫升)处理巨噬细胞系(RAW 264.7)18小时以诱导细胞因子释放。将这些细胞的条件培养基(5%,体积/体积)添加到无菌条件下分离并孵育的大鼠附睾脂肪细胞中。孵育后,洗涤脂肪细胞,并在进一步孵育1小时后测定脂解速率(甘油释放)。条件培养基使脂解增加约2.7倍,在6 - 12小时后可检测到,24小时达到最大值,在洗涤细胞后48小时可逆转。条件培养基的作用可被抗小鼠肿瘤坏死因子-α(TNFα)的中和抗体逆转,直接添加重组人TNFα(0.1 - 50纳克/毫升)可重现该作用,半数有效浓度约为3纳克/毫升。通过使用针对细菌表达的HSL酶96个氨基酸部分产生的抗体进行的Western免疫印迹法,研究了TNF对激素敏感性脂肪酶(HSL;脂解的限速酶)表达的影响。TNF处理未改变免疫反应性HSL的浓度。从这些数据我们得出结论:1)巨噬细胞响应脂多糖释放一种细胞因子,该细胞因子刺激新鲜分离的脂肪细胞中的脂解;2)TNFα可解释这种作用的大部分,甚至可能全部;3)TNFα通过不涉及HSL表达增加的机制增加脂解速率。基于TNFα刺激的时间依赖性方面以及免疫反应性HSL缺乏变化,这些发现提示该酶存在TNF诱导的翻译后修饰。

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