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大鼠垂体促性腺激素释放激素受体在非洲爪蟾卵母细胞中的功能表达

Functional expression of rat pituitary gonadotrophin-releasing hormone receptors in Xenopus oocytes.

作者信息

Eidne K A, McNiven A I, Taylor P L, Plant S, House C R, Lincoln D W, Yoshida S

机构信息

MRC Reproductive Biology Unit, Centre for Reproductive Biology, Edinburgh, United Kingdom.

出版信息

J Mol Endocrinol. 1988 Nov;1(3):R9-12. doi: 10.1677/jme.0.001r009.

Abstract

Expression of receptors for the hypothalamic regulatory peptide, gonadotrophin-releasing hormone (GnRH), was investigated by intracellular recording from Xenopus oocytes injected with poly(A)+ mRNA isolated from rat anterior pituitary glands. Membrane depolarizations were induced in oocytes in a dose-dependent fashion following the application of GnRH (10nM - 1 microM) or a GnRH superactive agonist, buserelin (1nM - 1 microM). The response was reversibly blocked by the addition of a GnRH antagonist (1 microM). TRH (10nM - 1 microM) had no effect on most of these oocytes. In contrast, some other oocytes which showed no responses to GnRH or to the GnRH agonist, displayed depolarizing responses to TRH (10nM - 1 microM). A relatively small number of oocytes responded to both ligands. Control oocytes did not respond to the GnRH analogues or to TRH. This successful expression of the GnRH receptor could provide a new approach to the study of the receptor, and serve as a means for the isolation and cloning of the encoding genes.

摘要

利用从大鼠垂体前叶分离的聚腺苷酸尾(poly(A)+)信使核糖核酸(mRNA)注射非洲爪蟾卵母细胞,通过细胞内记录法研究下丘脑调节肽促性腺激素释放激素(GnRH)受体的表达。在应用GnRH(10纳摩尔 - 1微摩尔)或GnRH超活性激动剂布舍瑞林(1纳摩尔 - 1微摩尔)后,卵母细胞以剂量依赖方式诱导膜去极化。加入GnRH拮抗剂(1微摩尔)可使反应可逆性阻断。促甲状腺激素释放激素(TRH,10纳摩尔 - 1微摩尔)对大多数这些卵母细胞无作用。相反,一些对GnRH或GnRH激动剂无反应的其他卵母细胞,对TRH(10纳摩尔 - 1微摩尔)呈现去极化反应。相对少数的卵母细胞对两种配体均有反应。对照卵母细胞对GnRH类似物或TRH无反应。GnRH受体的这种成功表达可为受体研究提供新方法,并作为分离和克隆编码基因的手段。

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