Tilly J L, Tilly K I, Kenton M L, Johnson A L
Department of Population Dynamics, Johns Hopkins University, Baltimore, Maryland 21205-2179.
Endocrinology. 1995 Jan;136(1):232-41. doi: 10.1210/endo.136.1.7828536.
The loss of ovarian follicles through atresia, which accounts for greater than 99% of postnatal female germ cell depletion, is mediated through apoptotic cell death. Although recent data have shown that apoptosis in granulosa cells of ovarian follicles can be hormonally manipulated, the molecular mechanisms responsible for transducing external signals remain to be elucidated. Herein we have characterized changes in the expression of the bcl-2 protooncogene (an inhibitor of apoptosis), the bax gene (an inducer of apoptosis), and the bcl-x gene (which encodes both bcl-xlong, an inhibitor of apoptosis, and bcl-xshort, an inducer of apoptosis) during gonadotropin-stimulated follicular development in vivo and during atresia of antral follicles incubated in vitro. Complementary DNA fragments corresponding to rat bcl-2, rat bax, and rat bcl-x coding sequences were obtained by the reverse transcription-polymerase chain reaction (RT-PCR) technique using total RNA prepared from immature rat ovaries. Northern blot analysis of steady-state bcl-2, bax, and bcl-x messenger RNA (mRNA) levels in total RNA prepared from ovaries of immature rats before and after in vivo priming with 10 IU equine CG (eCG) revealed that eCG-induced follicular growth and survival were associated with a relatively constitutive level of bcl-2 and bcl-x expression but markedly reduced levels of bax mRNA (29 +/- 5% of saline-treated control animals). Using the RT-PCR technique coupled with Southern blot hybridization analysis to distinguish the long vs. short forms of bcl-x (which differ in size by 189 base pairs), it was determined that bcl-xlong was the predominant message expressed by granulosa cells of eCG-primed ovaries. The eCG-mediated decrease in bax expression, coupled with a maintenance of bcl-2 and bcl-xlong mRNA levels, were associated with a pronounced reduction in the extent of granulosa cell apoptosis. In contrast, the induction of apoptosis in a homogeneous population of healthy antral follicles by incubation in vitro without tropic support was associated with an significant increase in bax mRNA levels to 220 +/- 10% of those detected in freshly isolated, healthy follicles. Moreover, bcl-xlong message levels were significantly reduced in follicles incubated for 24 h to 69 +/- 4% of those levels detected in freshly isolated, healthy follicles. However, no significant change in the level of bcl-2 mRNA was detected.(ABSTRACT TRUNCATED AT 250 WORDS)
通过闭锁导致的卵巢卵泡丢失占出生后雌性生殖细胞耗竭的99%以上,这是由凋亡性细胞死亡介导的。尽管最近的数据表明卵巢卵泡颗粒细胞中的凋亡可通过激素调控,但负责转导外部信号的分子机制仍有待阐明。在此,我们描述了在体内促性腺激素刺激的卵泡发育过程中以及体外培养的窦状卵泡闭锁过程中,bcl-2原癌基因(一种凋亡抑制剂)、bax基因(一种凋亡诱导剂)和bcl-x基因(其编码bcl-xlong,一种凋亡抑制剂,以及bcl-xshort,一种凋亡诱导剂)表达的变化。使用从未成熟大鼠卵巢制备的总RNA,通过逆转录-聚合酶链反应(RT-PCR)技术获得了与大鼠bcl-2、大鼠bax和大鼠bcl-x编码序列相对应的互补DNA片段。对用10 IU马绒毛膜促性腺激素(eCG)进行体内预处理前后的未成熟大鼠卵巢制备的总RNA中稳态bcl-2、bax和bcl-x信使RNA(mRNA)水平进行Northern印迹分析,结果显示eCG诱导的卵泡生长和存活与bcl-2和bcl-x相对稳定的表达水平相关,但bax mRNA水平显著降低(为盐水处理对照动物的29±5%)。使用RT-PCR技术结合Southern印迹杂交分析来区分bcl-x的长、短形式(其大小相差189个碱基对),确定bcl-xlong是eCG预处理卵巢颗粒细胞表达的主要信息。eCG介导的bax表达降低,以及bcl-2和bcl-xlong mRNA水平的维持,与颗粒细胞凋亡程度的显著降低相关。相反,在无促性腺激素支持的体外培养中,健康窦状卵泡均匀群体中凋亡的诱导与bax mRNA水平显著增加至新鲜分离的健康卵泡中检测水平的220±10%相关。此外,培养24小时的卵泡中bcl-xlong信息水平显著降低至新鲜分离的健康卵泡中检测水平的69±4%。然而,未检测到bcl-2 mRNA水平有显著变化。(摘要截短于250字)