Yuh K C, Possley R M, Brabec R K, Keyes P L
J Reprod Fertil. 1986 Jan;76(1):267-77. doi: 10.1530/jrf.0.0760267.
On the day after ovulation, the thecal tissue and associated mural granulosa lutein cells of the rabbit corpus luteum were separated from the granulosa lutein 'core' by dissection and these tissues were cultured separately or together (whole corpus luteum) in defined medium for 10 days on stainless-steel grids. The medium was changed completely every 24 h. Replicate tissues were cultured with testosterone (10 ng/ml), but no other hormones were added to the medium. Progesterone production increased during the first 2 days of culture for whole corpus luteum, granulosa lutein cells and the thecal compartment which also included granulosa lutein cells. After 3 days, the production of progesterone declined gradually, but was still detectable on Day 10. The production of the metabolite, 20 alpha-dihydroprogesterone, by whole corpus luteum was equal to or greater than that of progesterone. Without the addition of testosterone, the granulosa lutein cells produced little (10 pg/culture) oestradiol during 1 day of culture, but the thecal compartment and whole corpus luteum each produced about 100 pg/culture on Day 1 and declining quantities over the next 2 days. In the presence of testosterone added to the medium, the formation of oestradiol was greatly increased for all tissues for 5-6 days of culture, after which time oestradiol was no longer detectable with or without testosterone in medium. Transmission electron microscopy of cells after 10-12 days of culture revealed fine structure that is characteristic of luteal cells, including abundant smooth endoplasmic reticulum, lipid droplets, and junctions between the luteal cells. The corpus luteum in culture resembles the corpus luteum in situ in that steroidogenesis and differentiation can proceed for a period after ovulation without extrinsic hormonal stimulation.
排卵后的第二天,通过解剖将兔黄体的膜组织及相关的壁颗粒黄体细胞与颗粒黄体“核心”分离,这些组织分别或一起(整个黄体)在限定培养基中于不锈钢网格上培养10天。每24小时完全更换一次培养基。复制的组织与睾酮(10 ng/ml)一起培养,但培养基中未添加其他激素。对于整个黄体、颗粒黄体细胞以及也包含颗粒黄体细胞的膜部分,在培养的前两天孕酮产量增加。3天后,孕酮产量逐渐下降,但在第10天仍可检测到。整个黄体产生的代谢产物20α - 二氢孕酮的产量等于或高于孕酮。不添加睾酮时,颗粒黄体细胞在培养1天期间产生少量(10 pg/培养物)雌二醇,但膜部分和整个黄体在第1天各产生约100 pg/培养物,在接下来的2天中产量下降。在培养基中添加睾酮的情况下,所有组织在培养5 - 6天时雌二醇的形成大幅增加,此后无论培养基中有无睾酮,都不再能检测到雌二醇。培养10 - 12天后细胞的透射电子显微镜检查显示出黄体细胞特有的精细结构,包括丰富的滑面内质网、脂滴以及黄体细胞之间的连接。培养的黄体类似于原位黄体,即排卵后在没有外部激素刺激的情况下,类固醇生成和分化可以持续一段时间。