LaPolt P S, Soto D, Su J G, Campen C A, Vaughan J, Vale W, Hsueh A J
Department of Reproductive Medicine, University of California, San Diego School of Medicine, La Jolla 92093.
Mol Endocrinol. 1989 Oct;3(10):1666-73. doi: 10.1210/mend-3-10-1666.
Recent reports suggest that activin (the dimer of inhibin beta subunits with FSH-releasing activity) has specific receptors on ovarian granulosa cells. The present study examined the effects of purified porcine activin on inhibin secretion and mRNA levels in granulosa cells obtained from immature, estrogen-treated rats. Cells were cultured for 48 h in culture media, or media containing FSH (10 ng/ml) and/or activin (30 ng/ml). Western blot analyses performed with affinity-purified antisera to inhibin alpha- and beta A-subunits revealed that treatment with either FSH or activin increased the secretion of inhibin alpha beta dimer (Mr 30,000), with a further increase after cotreatment. These results were confirmed by an inhibin alpha-subunit RIA, which revealed 7-, 14-, and 71-fold increases in the secretion of immunoreactive inhibin-alpha by activin, FSH, and activin plus FSH, respectively. TGF beta, a structural homolog of activin, also stimulated inhibin release, whereas follistatin was ineffective. Total RNA from cultured cells was hybridized with 32P-labeled inhibin alpha-subunit cRNA or beta-actin cDNA probes, and inhibin-alpha message levels were normalized with beta-actin mRNA levels. Northern blot analysis revealed that treatment with FSH and activin increased hybridization of a 1.5 kilobase (kb) message, corresponding to the inhibin alpha-subunit mRNA. Slot blot analyses indicated a 6- and 8-fold stimulation of inhibin alpha-subunit mRNA levels by FSH and activin, respectively.(ABSTRACT TRUNCATED AT 250 WORDS)
最近的报告表明,激活素(具有促卵泡生成素释放活性的抑制素β亚基二聚体)在卵巢颗粒细胞上有特异性受体。本研究检测了纯化的猪激活素对从未成熟、经雌激素处理的大鼠获得的颗粒细胞中抑制素分泌及mRNA水平的影响。细胞在培养基中培养48小时,或在含有促卵泡生成素(10 ng/ml)和/或激活素(30 ng/ml)的培养基中培养。用针对抑制素α和βA亚基的亲和纯化抗血清进行的蛋白质印迹分析显示,促卵泡生成素或激活素处理均可增加抑制素αβ二聚体(分子量30,000)的分泌,联合处理后进一步增加。这些结果通过抑制素α亚基放射免疫分析得到证实,该分析显示激活素、促卵泡生成素以及激活素加促卵泡生成素处理后,免疫反应性抑制素α的分泌分别增加了7倍、14倍和71倍。激活素的结构同源物转化生长因子β也刺激抑制素释放,而卵泡抑素则无效。将培养细胞的总RNA与32P标记的抑制素α亚基cRNA或β-肌动蛋白cDNA探针杂交,并用β-肌动蛋白mRNA水平对抑制素α信息水平进行标准化。Northern印迹分析显示,促卵泡生成素和激活素处理增加了对应于抑制素α亚基mRNA的1.5千碱基(kb)信息的杂交。狭缝印迹分析表明,促卵泡生成素和激活素分别对抑制素α亚基mRNA水平有6倍和8倍的刺激作用。(摘要截短至250字)