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孕酮对人子宫内膜器官培养物中蜕膜催乳素产生的影响。

Effects of progesterone on decidual prolactin production by organ cultures of human endometrium.

作者信息

Maslar I A, Ansbacher R

出版信息

Endocrinology. 1986 May;118(5):2102-8. doi: 10.1210/endo-118-5-2102.

Abstract

The effects of progesterone on decidual PRL (dPRL) production by human endometrium were investigated by culturing explants of proliferative (n = 20) and secretory (n = 12) endometrium in Dulbecco's Modified Eagle's Medium supplemented with 10 mM HEPES buffer, 0.1% gelatin (wt/vol), and antibiotics for 6 days and in medium containing 50 ng/ml of progesterone for 6-28 days. The culture medium was replaced daily, and the spent medium was assayed for dPRL. Representative explants were fixed for histological examination after 1, 2, 7, 14, and 28 days in vitro. When explants of endometrium obtained throughout the cycle were cultured in the presence of progesterone, dPRL production was stimulated. Proliferative endometria required 2-5 days in culture before dPRL was measured in the medium. Thereafter, dPRL production increased gradually for the duration of the experiment. Progesterone also induced glandular secretion and stromal differentiation (decidualization) in these tissues. Cultures of proliferative endometrium that did not receive progesterone did not produce detectable amounts of dPRL. When explants of secretory endometrium were cultured in DMEM without exogenous progesterone, dPRL was released into the medium for 2-5 days; however, dPRL production by the cultures that did not receive progesterone declined to undetectable levels, while that by the progesterone-treated cultures increased steadily. Explants of both proliferative and secretory endometrium that were fixed for histological examination after 28 days of culture in the presence of progesterone were composed predominately of large stromal cells that resembled the decidual cells of pregnancy endometrium.

摘要

通过在补充有10 mM HEPES缓冲液、0.1%明胶(重量/体积)和抗生素的杜尔贝科改良伊格尔培养基中培养增殖期(n = 20)和分泌期(n = 12)子宫内膜外植体6天,并在含有50 ng/ml孕酮的培养基中培养6 - 28天,研究了孕酮对人子宫内膜蜕膜催乳素(dPRL)产生的影响。每天更换培养基,并对用过的培养基进行dPRL检测。在体外培养1、2、7、14和28天后,将代表性外植体固定用于组织学检查。当在整个周期获得的子宫内膜外植体在孕酮存在下培养时,dPRL的产生受到刺激。增殖期子宫内膜在培养基中检测到dPRL之前需要培养2 - 5天。此后,在实验期间dPRL的产生逐渐增加。孕酮还诱导这些组织中的腺体分泌和基质分化(蜕膜化)。未接受孕酮的增殖期子宫内膜培养物未产生可检测量的dPRL。当分泌期子宫内膜外植体在无外源性孕酮的DMEM中培养时,dPRL释放到培养基中持续2 - 5天;然而,未接受孕酮的培养物中dPRL的产生下降到检测不到的水平,而接受孕酮处理的培养物中dPRL的产生则稳步增加。在孕酮存在下培养28天后固定用于组织学检查的增殖期和分泌期子宫内膜外植体,主要由类似于妊娠子宫内膜蜕膜细胞的大基质细胞组成。

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