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从初级和次级卵泡分离的猪颗粒细胞在体外对促卵泡激素、8-溴环磷酸腺苷和表皮生长因子的反应。

Response of porcine granulosa cells isolated from primary and secondary follicles to FSH, 8-bromo-cAMP and epidermal growth factor in vitro.

作者信息

Morbeck D E, Flowers W L, Britt J H

机构信息

Department of Animal Science, North Carolina State University, Raleigh 27695-7621.

出版信息

J Reprod Fertil. 1993 Nov;99(2):577-84. doi: 10.1530/jrf.0.0990577.

Abstract

A cell culture system was developed to study the function of porcine granulosa cells from primary and secondary follicles. Primary follicles were isolated from 1- to 3-day-old pigs. Secondary follicles were isolated from 50- to 60-day-old pigs. Follicles were isolated after a digestion for 15 min with 0.25% trypsin followed by 15 min with 1000 U DNAase. Follicles were plated at 100 primary follicles or 30 secondary follicles per well in 48-well plates and cultured in media containing 10% fetal bovine serum (FBS). During initial plating, follicles attached to the plate and cells spread from the point of attachment. This resulted in monolayer cultures of granulosa cells from primary or secondary follicles. On day 4 of culture, media were replaced with 0.5 ml media containing one of the following treatments: control (media only); 10% FBS; 100 ng FSH; 2 mmol 8-bromo-cAMP l-1 or 50 ng epidermal growth factor (EGF). Media and cells were harvested on day 6, after 2 days of treatment. FBS and EGF increased DNA in granulosa cell cultures from primary or secondary follicles (P < 0.01). Treatment with 8-bromo-cAMP increased DNA in granulosa cell cultures from primary but not from secondary follicles (P < 0.05). Conversely, treatment with FSH increased DNA in granulosa cell cultures from secondary but not from primary follicles (P < 0.05).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

开发了一种细胞培养系统,用于研究来自初级和次级卵泡的猪颗粒细胞的功能。初级卵泡从1至3日龄的猪中分离。次级卵泡从50至60日龄的猪中分离。卵泡先用0.25%胰蛋白酶消化15分钟,然后用1000 U脱氧核糖核酸酶消化15分钟后进行分离。将卵泡以每孔100个初级卵泡或30个次级卵泡接种到48孔板中,并在含有10%胎牛血清(FBS)的培养基中培养。在最初接种时,卵泡附着在板上,细胞从附着点扩散。这导致了来自初级或次级卵泡的颗粒细胞单层培养。在培养的第4天,将培养基换成0.5 ml含有以下处理之一的培养基:对照(仅培养基);10% FBS;100 ng促卵泡激素(FSH);2 mmol 8-溴环磷酸腺苷(8-bromo-cAMP)l-1或50 ng表皮生长因子(EGF)。在处理2天后的第6天收集培养基和细胞。FBS和EGF增加了来自初级或次级卵泡的颗粒细胞培养物中的DNA(P < 0.01)。用8-溴环磷酸腺苷处理增加了来自初级卵泡而非次级卵泡的颗粒细胞培养物中的DNA(P < 0.05)。相反,用FSH处理增加了来自次级卵泡而非初级卵泡的颗粒细胞培养物中的DNA(P < 0.05)。(摘要截断于250字)

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