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未成熟大鼠睾丸间质细胞DNA合成对生长因子的需求

Growth factor requirements for DNA synthesis by Leydig cells from the immature rat.

作者信息

Khan S, Teerds K, Dorrington J

机构信息

Banting and Best Department of Medical Research, University of Toronto, Canada.

出版信息

Biol Reprod. 1992 Mar;46(3):335-41. doi: 10.1095/biolreprod46.3.335.

Abstract

Puberty in the male is dependent upon the elevated production of testosterone by the Leydig cells. LH affects this increase in testosterone output by increasing the total number of Leydig cells in the testis and by stimulating the steroidogenic pathway in these cells. Since Leydig cell proliferation is a prerequisite for the onset of puberty, we have examined the ability of LH and growth factors known to be present in the testis to promote DNA synthesis. Leydig cells were isolated from 21-day-old rats, cultured in serum-free medium for 48 h to become quiescent, and then treated with LH and growth factors for 18 h. [3H]Thymidine incorporation into DNA was assessed over the subsequent 4-h incubation period. Cells in control cultures incorporated low levels of [3H]thymidine into DNA and were stimulated after treatment with LH (100 ng/ml). Insulin/insulin-like growth factor-1 (IGF-1) and transforming growth factor-alpha (TGF-alpha), previously localized in Leydig cells by immunohistochemistry, also stimulated [2H]thymidine incorporation into DNA. The responses of the Leydig cells to maximum levels of insulin and TGF-alpha were dependent on the cell density. Insulin and TGF-alpha alone and in combination increased the number of cells labeled with [3H]thymidine, as assessed by autoradiography. TGF-beta, known to be secreted by Sertoli cells, also stimulated DNA synthesis under basal conditions, but the maximum response was significantly lower than that achieved in the presence of TGF-alpha.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

男性青春期依赖于睾丸间质细胞睾酮分泌增加。促黄体生成素(LH)通过增加睾丸间质细胞总数和刺激这些细胞的类固醇生成途径来影响睾酮分泌增加。由于间质细胞增殖是青春期开始的先决条件,我们研究了已知存在于睾丸中的LH和生长因子促进DNA合成的能力。从21日龄大鼠分离间质细胞,在无血清培养基中培养48小时使其静止,然后用LH和生长因子处理18小时。在随后4小时的孵育期内评估[3H]胸腺嘧啶掺入DNA的情况。对照培养物中的细胞将低水平的[3H]胸腺嘧啶掺入DNA,用LH(100 ng/ml)处理后受到刺激。胰岛素/胰岛素样生长因子-1(IGF-1)和转化生长因子-α(TGF-α),先前通过免疫组织化学定位在间质细胞中,也刺激[3H]胸腺嘧啶掺入DNA。间质细胞对最大水平胰岛素和TGF-α的反应取决于细胞密度。通过放射自显影评估,单独和联合使用胰岛素和TGF-α增加了用[3H]胸腺嘧啶标记的细胞数量。已知由支持细胞分泌的TGF-β在基础条件下也刺激DNA合成,但最大反应明显低于存在TGF-α时的反应。(摘要截短至250字)

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