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促黄体生成激素释放激素(LHRH)在无血清培养中未能影响大鼠垂体原基中促黄体生成素(LH)细胞的分化。

Failure of luteinizing hormone-releasing hormone (LHRH) to affect the differentiation of LH cells in the rat hypophysial primordium in serum-free culture.

作者信息

Watanabe Y G

机构信息

Department of Anatomy, Sapporo Medical College, Japan.

出版信息

Cell Tissue Res. 1987 Oct;250(1):35-42. doi: 10.1007/BF00214651.

Abstract

The aims of this study were to investigate the differentiating capacity of adenohypophysial LH cells in a serum-free culture medium and to test whether cytogenesis is affected by synthetic LHRH. The adenohypophysial primordia of fetal rats were isolated on days 11.5 and 12.5 of gestation and cultured without serum for 10 and 9 days, respectively, in synthetic Medium 199 or alpha MEM. Immunohistochemical examination using the PAP method revealed that most culture explants, apart from a few degenerate ones, contained LH cells. In comparison with Medium 199, which has been widely used as a culture medium for hypophysial explants, alpha MEM gave far better results and the primordia cultured in this medium showed better tissue growth and contained a greater number of LH cells. Administration of synthetic LHRH (10 ng/ml) on the first day of culturing had no effect on the number of LH cells, no matter whether or not the culture medium was supplemented with insulin, transferrin or thyroxine. These results suggest that at the early developmental stage LHRH is not essential for the differentiation and/or proliferation of LH cells.

摘要

本研究的目的是研究腺垂体促黄体生成素(LH)细胞在无血清培养基中的分化能力,并测试细胞生成是否受合成促性腺激素释放激素(LHRH)的影响。在妊娠第11.5天和12.5天分离胎鼠的腺垂体原基,分别在合成199培养基或α-改良 Eagle 培养基(α-MEM)中无血清培养10天和9天。使用过氧化物酶抗过氧化物酶(PAP)法进行免疫组织化学检查显示,除了少数退化的外植体,大多数培养外植体都含有LH细胞。与广泛用作垂体外植体培养基的199培养基相比,α-MEM的效果要好得多,在此培养基中培养的原基显示出更好的组织生长,并且含有更多的LH细胞。在培养的第一天添加合成LHRH(10 ng/ml)对LH细胞的数量没有影响,无论培养基是否添加胰岛素、转铁蛋白或甲状腺素。这些结果表明,在发育早期,LHRH对于LH细胞的分化和/或增殖不是必需的。

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