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促性腺激素释放激素受体与培养的垂体促性腺细胞的反应

Gonadotrophin releasing hormone receptors and the response of pituitary gonadotrophs in culture.

作者信息

Bérault A, Jansen de Almeida Catanho M T, Théoleyre M, Jutisz M

出版信息

J Endocrinol. 1983 Sep;98(3):391-9. doi: 10.1677/joe.0.0980391.

Abstract

We have investigated the effect of the time of culture on cell number, cell content of LH, cell responsiveness to gonadotrophin releasing hormone (GnRH) and binding parameters of GnRH in rat anterior pituitary cells in culture. Although a decrease in the cell number was observed during the culture period, the cell content of LH remained unchanged. The receptor affinity (Ka) in acutely dispersed cells was 0.86 X 10(7) l/mol for [3H]GnRH and 1.36 X 10(10) l/mol for a highly potent agonist, [D-Ser(But)6]GnRH(1-9)nonapeptide-ethylamide (GnRH-A). The affinity and binding capacity (0.3 fmol/10(6) cells) for iodinated GnRH-A did not change significantly during the 6-day culture period. On the contrary, the values of Ka and binding capacity (257 fmol/10(6) cells) for tritiated GnRH decreased by about 50% between days 1 and 6 of culture. Our results suggest that 125I-labelled GnRH-A binds mostly to high-affinity and low-capacity receptor sites, while [3H]GnRH, which must be used at a higher concentration, also binds to low-affinity, high-capacity binding sites and is therefore useless for the measurement of GnRH receptor binding affinity and binding capacity. Since the biological response of the cells to GnRH increased with the time of culture, it is concluded that although GnRH action is receptor-mediated, binding capacity and biological activity are not necessarily correlated.

摘要

我们研究了培养时间对培养的大鼠垂体前叶细胞数量、促黄体生成素(LH)的细胞含量、细胞对促性腺激素释放激素(GnRH)的反应性以及GnRH结合参数的影响。尽管在培养期间观察到细胞数量减少,但LH的细胞含量保持不变。急性分散细胞中,[³H]GnRH的受体亲和力(Ka)为0.86×10⁷ l/mol,高效激动剂[D-Ser(But)⁶]GnRH(1-9)九肽乙酰胺(GnRH-A)的受体亲和力为1.36×10¹⁰ l/mol。在6天的培养期内,碘化GnRH-A的亲和力和结合容量(0.3 fmol/10⁶细胞)没有明显变化。相反,在培养的第1天至第6天之间,氚标记GnRH的Ka值和结合容量(257 fmol/10⁶细胞)下降了约50%。我们的结果表明,¹²⁵I标记的GnRH-A主要与高亲和力、低容量的受体位点结合,而[³H]GnRH必须以更高的浓度使用,它也与低亲和力、高容量的结合位点结合,因此对于测量GnRH受体结合亲和力和结合容量没有用处。由于细胞对GnRH的生物学反应随培养时间增加,因此得出结论,尽管GnRH作用是受体介导的,但结合容量和生物学活性不一定相关。

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