Tsuji M, Shima H, Cunha G R
Department of Anatomy, University of California, San Francisco 94143.
Endocrinology. 1991 Apr;128(4):1805-11. doi: 10.1210/endo-128-4-1805.
Male mouse urogenital ridges (URs) at 15.5 days of gestation (vaginal plug = day 0) containing Wolffian (WDs) and Mullerian ducts were cultured for 4 days with or without gonads in serum-free medium (1:1 mixture of Dulbecco's modified Eagle's medium and Ham's F-12 supplemented with insulin, transferrin, cholera toxin, epidermal growth factor, and BSA). URs without gonads were grown in serum-free medium with testosterone (T, 10(-7) M), 5 alpha-dihydrotestosterone (DHT, 10(-8) M), T (10(-7) M) plus cyproterone acetate (antiandrogen, 10(-5) M), or T (10(-8) M) plus 390 MSD (17 beta-N, N-diisopropylcarbamoyl-4-aza-5 alpha- androstan-3-one, an inhibitor of 5 alpha-reductase, 10(-5) M). After 4 days of culture the number of epididymal curvatures that appeared in the upper portion of WDs were quantified. DNA content of URs grown in serum-free medium was also measured. Both T and DHT increased DNA contents in a dose- (T = 10(-8) to 10(-10) M, DHT = 10(-9) to 10(-11) M) and time-dependent manner. DHT was approximately 10-fold more effective than T in eliciting epididymal coiling and increasing DNA content of URs. The effects of T or DHT were mimicked by coculture with fetal testes. Epididymal coiling and an increase in DNA content occurred in URs grown in the presence of T plus 390 MSD. By contrast, URs cultured without androgens or with T plus cyproterone acetate failed to undergo epididymal coiling and to increase DNA content. The conversion rate per mg protein of [1 beta, 2 beta-3H]T into [3H]DHT was 0.30-fold lower in 15.5 day URs cultured over a 4-day period in comparison to urogenital sinuses whose development is known to be dependent upon DHT. These data suggest that T is an important hormone in the development of the upper portion of WDs, although it is not possible to exclude a role for DHT in the development of the epididymis.
取妊娠15.5天(以出现阴栓日为第0天)的雄性小鼠泌尿生殖嵴(URs),其包含中肾管(WDs)和苗勒管,在无血清培养基(由杜氏改良 Eagle 培养基和哈姆氏F-12按1:1混合,添加胰岛素、转铁蛋白、霍乱毒素、表皮生长因子和牛血清白蛋白)中培养4天,培养过程中有无性腺。无性腺的泌尿生殖嵴在含睾酮(T,10⁻⁷ M)、5α-双氢睾酮(DHT,10⁻⁸ M)、T(10⁻⁷ M)加醋酸环丙孕酮(抗雄激素,10⁻⁵ M)或T(10⁻⁸ M)加390 MSD(17β-N,N-二异丙基氨基甲酰-4-氮杂-5α-雄甾-3-酮,5α-还原酶抑制剂,10⁻⁵ M)的无血清培养基中培养。培养4天后,对中肾管上部出现的附睾曲度数量进行定量。同时测定在无血清培养基中培养的泌尿生殖嵴的DNA含量。T和DHT均以剂量依赖(T = 10⁻⁸至10⁻¹⁰ M,DHT = 10⁻⁹至10⁻¹¹ M)和时间依赖的方式增加DNA含量。在引发附睾卷曲和增加泌尿生殖嵴的DNA含量方面,DHT的效力约为T的10倍。与胎儿睾丸共培养可模拟T或DHT的作用。在T加390 MSD存在下培养的泌尿生殖嵴出现附睾卷曲且DNA含量增加。相比之下,在无雄激素或T加醋酸环丙孕酮培养的泌尿生殖嵴未发生附睾卷曲且DNA含量未增加。在15.5天的泌尿生殖嵴中培养4天,每毫克蛋白质将[1β, 2β-³H]T转化为[³H]DHT的转化率比已知其发育依赖DHT的泌尿生殖窦低0.30倍。这些数据表明,T是中肾管上部发育中的一种重要激素,尽管不能排除DHT在附睾发育中的作用。