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利用生物活性瘦素免疫黏附素克隆和鉴定人瘦素受体

Cloning and characterization of a human leptin receptor using a biologically active leptin immunoadhesin.

作者信息

Luoh S M, Di Marco F, Levin N, Armanini M, Xie M H, Nelson C, Bennett G L, Williams M, Spencer S A, Gurney A, de Sauvage F J

机构信息

Department of Molecular Oncology, Genentech Inc., South San Francisco, California 94080, USA.

出版信息

J Mol Endocrinol. 1997 Feb;18(1):77-85. doi: 10.1677/jme.0.0180077.

Abstract

Leptin, the product of the ob gene, is a hormone secreted by fat cells which is primarily involved in the regulation of body weight. We have generated a leptin immunoadhesin (leptin-IgG) which was more potent than leptin alone at reducing body weight and food intake when injected into ob/ob mice. This molecule was used to identify high affinity binding sites on human embryonic 293 kidney cells and subsequently to isolate a cDNA encoding the leptin receptor from this cell line by expression cloning. This receptor corresponds to the short form of the recently isolated leptin receptor. Analysis of the expression pattern of the two forms of receptor by Northern blot, in situ hybridization and quantitative PCR showed that the receptor is expressed in most tissues but that the long form is prevalent in the hypothalamus.

摘要

瘦素是ob基因的产物,是一种由脂肪细胞分泌的激素,主要参与体重调节。我们制备了一种瘦素免疫粘附素(瘦素-IgG),当将其注射到ob/ob小鼠体内时,它在减轻体重和食物摄入量方面比单独的瘦素更有效。该分子用于鉴定人胚胎293肾细胞上的高亲和力结合位点,随后通过表达克隆从该细胞系中分离出编码瘦素受体的cDNA。该受体对应于最近分离的瘦素受体的短形式。通过Northern印迹、原位杂交和定量PCR分析两种形式受体的表达模式表明,该受体在大多数组织中表达,但长形式在下丘脑中普遍存在。

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