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细胞因子、儿茶酚胺和过氧化物酶体增殖物激活受体γ对3T3-L1脂肪细胞中触珠蛋白基因表达的调控

Regulation of haptoglobin gene expression in 3T3-L1 adipocytes by cytokines, catecholamines, and PPARgamma.

作者信息

do Nascimento Claudia Oller, Hunter Leif, Trayhurn Paul

机构信息

Liverpool Centre for Nutritional Genomics, Neuroendocrine and Obesity Biology Unit, Department of Medicine, University of Liverpool, University Clinical Departments, Duncan Building, Liverpool L69 3GA, UK.

出版信息

Biochem Biophys Res Commun. 2004 Jan 16;313(3):702-8. doi: 10.1016/j.bbrc.2003.12.008.

Abstract

Factors which regulate expression of the haptoglobin (acute phase reactant) gene in adipocytes have been examined using 3T3-L1 cells. Haptoglobin expression was observed by Northern blotting in each of the major white adipose tissue depots of mice (epididymal, subcutaneous, mesenteric, and perirenal) and in interscapular brown fat. Expression occurred in mature adipocytes, but not in the stromal-vascular fraction. In 3T3-L1 cells, haptoglobin mRNA was detected from day 4 after the induction of differentiation into adipocytes. Lipopolysaccharide and the cytokines, TNFalpha and interleukin-6, resulted in substantial increases in haptoglobin mRNA in 3T3-L1 adipocytes; the increase (7-fold) was highest with TNFalpha. Increases in haptoglobin mRNA level were also induced by dexamethasone, noradrenaline, isoprenaline, and a beta3-adrenoceptor agonist. In contrast, haptoglobin mRNA was reduced by nicotinic acid and the PPARgamma agonist, rosiglitazone. RT-PCR showed that the haptoglobin gene was expressed in human adipose tissue (subcutaneous, omental). It is concluded that haptoglobin gene expression in adipocytes is stimulated by inflammatory cytokines, glucocorticoids, and the sympathetic system, while activation of the PPARgamma nuclear receptor is strongly inhibitory.

摘要

利用3T3-L1细胞对调节脂肪细胞中触珠蛋白(急性期反应物)基因表达的因素进行了研究。通过Northern印迹法在小鼠的每个主要白色脂肪组织储存部位(附睾、皮下、肠系膜和肾周)以及肩胛间棕色脂肪中观察到了触珠蛋白的表达。表达发生在成熟脂肪细胞中,而不在基质血管部分。在3T3-L1细胞中,从诱导分化为脂肪细胞后的第4天开始检测到触珠蛋白mRNA。脂多糖以及细胞因子TNFα和白细胞介素-6导致3T3-L1脂肪细胞中触珠蛋白mRNA大幅增加;TNFα引起的增加(7倍)最高。地塞米松、去甲肾上腺素、异丙肾上腺素和β3-肾上腺素能受体激动剂也诱导了触珠蛋白mRNA水平的增加。相反,烟酸和PPARγ激动剂罗格列酮降低了触珠蛋白mRNA水平。RT-PCR表明触珠蛋白基因在人脂肪组织(皮下、网膜)中表达。得出的结论是,脂肪细胞中触珠蛋白基因的表达受到炎性细胞因子、糖皮质激素和交感神经系统的刺激,而PPARγ核受体的激活具有强烈的抑制作用。

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