Kiya T, Endo T, Goto T, Yamamoto H, Ito E, Kudo R, Behrman H R
Department of Obstetrics and Gynecology, Sapporo Medical University School of Medicine, Japan.
J Endocrinol Invest. 1998 May;21(5):276-83. doi: 10.1007/BF03350329.
There are two stages of luteal regression. The first stage is functional regression that is characterized by a decreased production of progesterone secretion; the second stage of structural involution is referred to as a structural luteolysis. In rodents, prolactin has a biphasic action on the corpus luteum. It is luteotrophic, but when exposed to functionally regressed corpora lutea it causes luteolysis. The objective of the present studies was to examine mechanisms of prolactin action in structural luteolysis, whether apoptosis is involved in this process, and to examine the possible association of cell proliferation signals as mediators of structural luteolysis. Prolactin-induced structural luteolysis was associated with apoptosis verified by terminal deoxynucleotidyl transferase (TdT)-mediated dUTP-biotin nick end labeling (TUNEL). Apoptotic cells made up about 3% of the cells 24 hours after the first injection of prolactin, a level that remained constant at all stages of structural luteolysis. Total ovarian weight and DNA content were decreased about 50% in 72 hours after induction of structural luteolysis by prolactin, The finding of about 3% of cells in apoptosis indicates apoptosis is a rapid process. Proliferating cell nuclear antigens (PCNA) of luteal cells were significantly decreased during functional luteal regression, but were conversely increased in structural luteolysis as shown by western blotting and immunohistochemistry. In general PCNA expression is reported to be decreased during structural involution, and there are no reports that have linked excess expression of PCNA with apoptosis and structural luteolysis. We speculate that an excessive increase in expression of PCNA which signals activation of cell proliferation creates a disorder in the signals involved with DNA synthesis. This disorder results in mitotic catastrophe and in the induction of apoptosis. Therefore the disorder of cell cycle signals in luteal cells are associated with prolactin induced apoptosis in structural luteolysis.
黄体退化有两个阶段。第一阶段是功能性退化,其特征是孕酮分泌减少;第二阶段是结构退化,称为结构性黄体溶解。在啮齿动物中,催乳素对黄体有双相作用。它具有黄体营养作用,但当作用于功能性退化的黄体时会导致黄体溶解。本研究的目的是研究催乳素在结构性黄体溶解中的作用机制,是否有细胞凋亡参与此过程,并研究细胞增殖信号作为结构性黄体溶解介质的可能关联。催乳素诱导的结构性黄体溶解与通过末端脱氧核苷酸转移酶(TdT)介导的dUTP-生物素缺口末端标记(TUNEL)验证的细胞凋亡相关。首次注射催乳素后24小时,凋亡细胞约占细胞总数的3%,在结构性黄体溶解的所有阶段该水平保持恒定。在催乳素诱导结构性黄体溶解72小时后,卵巢总重量和DNA含量下降约50%。约3%的细胞发生凋亡这一发现表明细胞凋亡是一个快速过程。黄体细胞的增殖细胞核抗原(PCNA)在功能性黄体退化期间显著降低,但如蛋白质印迹法和免疫组织化学所示,在结构性黄体溶解中反而增加。一般报道称在结构退化期间PCNA表达降低,且没有报道将PCNA的过度表达与细胞凋亡和结构性黄体溶解联系起来。我们推测,标志着细胞增殖激活的PCNA表达过度增加会导致参与DNA合成的信号紊乱。这种紊乱导致有丝分裂灾难并诱导细胞凋亡。因此,黄体细胞中细胞周期信号的紊乱与催乳素诱导的结构性黄体溶解中的细胞凋亡相关。