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肝脏X受体在人皮肤及毛囊皮脂腺单位中的表达与功能特性

Characterization of liver X receptor expression and function in human skin and the pilosebaceous unit.

作者信息

Russell Louise E, Harrison Wesley J, Bahta Adiam W, Zouboulis Christos C, Burrin Jacky M, Philpott Michael P

机构信息

Centre for Cutaneous Research and Centre for Endocrinology, Bart's and The London Queen Mary's School of Medicine and Dentistry, Queen Mary College, University of London, London, UK.

出版信息

Exp Dermatol. 2007 Oct;16(10):844-52. doi: 10.1111/j.1600-0625.2007.00612.x.

Abstract

The nuclear receptors liver X receptor alpha (LXRalpha) and liver X-receptor beta (LXRbeta) have a well documented role in cholesterol homeostasis and lipid metabolism within tissues and cells including the liver, small intestine and macrophages. In keratinocytes, LXRs have been shown to up-regulate differentiation in vitro via increased transcription of proteins of the AP1 complex and to down-regulate proliferation in vivo. In this study, we provide a detailed description of the location and possible role of LXRs within human skin and its associated glands and appendages. Using RT-PCR, Western blotting and immunohistochemistry, we have demonstrated expression of LXRalpha and LXRbeta mRNA and proteins in whole human skin as well as within a range of primary and immortalized human cell lines derived from human skin, hair follicle and sebaceous glands. Furthermore, we have shown that synthetic LXR specific agonists GW683965 and TO901317 significantly inhibit cell proliferation in primary epidermal keratinocytes, immortalized N/TERT keratinocytes and the immortalized SZ95 sebocyte line, and significantly increase lipogenesis in SZ95 sebocytes. In addition, we showed that the synthetic agonist TO901317 significantly reduced hair growth, in vitro.

摘要

核受体肝X受体α(LXRα)和肝X受体β(LXRβ)在包括肝脏、小肠和巨噬细胞在内的组织和细胞内的胆固醇稳态和脂质代谢中具有充分记录的作用。在角质形成细胞中,LXRs已被证明在体外通过增加AP1复合物蛋白的转录来上调分化,并在体内下调增殖。在本研究中,我们详细描述了LXRs在人类皮肤及其相关腺体和附属器中的定位和可能作用。使用逆转录聚合酶链反应(RT-PCR)、蛋白质印迹法和免疫组织化学,我们已经证明了LXRα和LXRβ mRNA及蛋白质在全层人类皮肤以及一系列源自人类皮肤、毛囊和皮脂腺的原代和永生化人类细胞系中的表达。此外,我们已经表明,合成的LXR特异性激动剂GW683965和TO901317显著抑制原代表皮角质形成细胞、永生化N/TERT角质形成细胞和永生化SZ95皮脂腺细胞系中的细胞增殖,并显著增加SZ95皮脂腺细胞中的脂肪生成。此外,我们还表明,合成激动剂TO901317在体外显著减少毛发生长。

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