首页> 美国卫生研究院文献>The Journal of Biophysical and Biochemical Cytology >Development of Phodopus sungorus brown preadipocytes in primary cell culture: effect of an atypical beta-adrenergic agonist insulin and triiodothyronine on differentiation mitochondrial development and expression of the uncoupling protein UCP
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Development of Phodopus sungorus brown preadipocytes in primary cell culture: effect of an atypical beta-adrenergic agonist insulin and triiodothyronine on differentiation mitochondrial development and expression of the uncoupling protein UCP

机译:初级细胞培养中日光藻棕色前脂肪细胞的发育:非典型β-肾上腺素能激动剂胰岛素和三碘甲状腺素对分化线粒体发育和解偶联蛋白UCP的表达的影响

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摘要

A new cellular model for the study of brown adipocyte development and differentiation in vitro is presented. Preadipocytes isolated from brown adipose tissue (BAT) of the djungarian dwarf hamster Phodopus sungorus are able to proliferate and differentiate in vitro into true brown adipocytes able to express the BAT marker protein the uncoupling protein (UCP). Whereas basal UCP expression is very low, its mRNA levels as well as the UCP detected by immunoblotting are highly increased by beta-adrenergic stimulation. The novel, atypical beta- adrenergic compound D7114 (ICI Pharmaceuticals, Macclesfield, Cheshire, England) was found to increase the number of adipocytes as well as UCP mRNA and UCP content of mitochondria, indicating the involvement of an atypical or beta 3 receptor. Insulin was found to play an important role in brown adipocyte differentiation and mitochondrial development, whereas T3 seemed to be implicated more directly in UCP expression. In a defined, serum-free medium a synergistic stimulatory action of insulin and T3 on UCP expression was found, which seems to involve a pathway different from that of beta-adrenergic UCP stimulation.
机译:提出了一种新的细胞模型,用于研究棕色脂肪细胞的体外发育和分化。从幼年侏儒仓鼠褐藻的棕色脂肪组织(BAT)中分离出的前脂肪细胞能够在体外增殖并分化为能够表达BAT标记蛋白解偶联蛋白(UCP)的真正的褐色脂肪细胞。尽管基础UCP表达非常低,但β-肾上腺素能刺激可大大提高其mRNA水平以及通过免疫印迹检测到的UCP。发现新型的,非典型的β-肾上腺素化合物D7114(ICI Pharmaceuticals,Macclesfield,英格兰柴郡)增加了线粒体的脂肪细胞数量以及UCP mRNA和UCP含量,表明其参与了非典型或β3受体。发现胰岛素在褐色脂肪细胞分化和线粒体发育中起重要作用,而T3似乎与UCP表达更直接相关。在确定的无血清培养基中,发现了胰岛素和T3对UCP表达的协同刺激作用,这似乎涉及与β-肾上腺素UCP刺激不同的途径。

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