Bicsak T A, Cajander S B, Peng X R, Ny T, LaPolt P S, Lu J K, Kristensen P, Tsafriri A, Hsueh A J
Department of Reproductive Medicine, University of California-San Diego, La Jolla 92093.
Endocrinology. 1989 Jan;124(1):187-94. doi: 10.1210/endo-124-1-187.
The regulation of tissue-type plasminogen activator (tPA) in rat oocytes during the periovulatory period, in early embryos, and in oocytes during induced follicular atresia was studied using a quantitative chromogenic substrate assay. Oocytes and early embryos were collected from three ovulation models: 1) intact immature female rats treated with PMSG, followed by hCG 48 h later; 2) hypophysectomized immature rats treated with PMSG, followed by a GnRH agonist (GnRHa) 56 h later; and 3) adult cyclic rats on the mornings of proestrus and estrus and up to 5 days after fertilization. In addition, follicular atresia was induced by either withdrawal of diethylstilbestrol (DES) for 2 days or injection of GnRHa for 2 days in hypophysectomized DES-implanted immature rats. Treatment with PMSG alone did not increase oocyte tPA content (5-20 microIU/oocyte) in either immature rat model, but treatment with either hCG or GnRHa induced meiotic maturation and ovulation and increased tPA activity to 80 and 140 microIU/oocyte 24 h after hCG and GnRHa treatment, respectively. Northern blot analysis of total RNA extracted from oocytes of PMSG-treated rats indicated the presence of a specific tPA message at 22S. tPA levels were low in preovulatory oocytes obtained on proestrus morning and increased in ovulated oocytes on estrus morning. After fertilization, tPA levels remained high in the embryos on days 1-4 of pregnancy, but dropped dramatically on day 5. Furthermore, oocytes from atretic follicles of hypophysectomized DES-implanted rats after either DES withdrawal or GnRHa treatment contained elevated levels of tPA, coincident with germinal vesicle breakdown (GVBD). Immunohistochemical staining revealed tPA antigen only in those oocytes that had undergone apparent meiotic maturation, as confirmed by GVBD. Thus, oocytes contain tPA mRNA and synthesize the active protease under a variety of stimuli which result in GVBD. The observed periovulatory increase in oocyte tPA activity, its maintenance until day 5 of pregnancy, and expression of tPA in nonovulatory oocytes of atretic follicles suggest diverse functions for the oocyte and embryo tPA.
利用定量显色底物分析法,研究了大鼠卵母细胞在排卵期、早期胚胎以及诱导卵泡闭锁期间组织型纤溶酶原激活物(tPA)的调控情况。卵母细胞和早期胚胎取自三种排卵模型:1)用孕马血清促性腺激素(PMSG)处理的未成熟雌性大鼠,48小时后再用绒毛膜促性腺激素(hCG)处理;2)垂体切除的未成熟大鼠,先用PMSG处理,56小时后再用促性腺激素释放激素激动剂(GnRHa)处理;3)成年周期性大鼠,在动情前期和动情期早晨以及受精后长达5天收集样本。此外,在垂体切除并植入己烯雌酚(DES)的未成熟大鼠中,通过停用DES 2天或注射GnRHa 2天诱导卵泡闭锁。单独用PMSG处理,在两种未成熟大鼠模型中均未增加卵母细胞tPA含量(5 - 20微国际单位/卵母细胞),但用hCG或GnRHa处理可诱导减数分裂成熟和排卵,并分别在hCG和GnRHa处理后24小时将tPA活性增加至80和140微国际单位/卵母细胞。对PMSG处理大鼠的卵母细胞提取的总RNA进行Northern印迹分析,结果表明在22S处存在特定的tPA信息。在动情前期早晨获得的排卵前卵母细胞中tPA水平较低,而在动情期早晨的排卵卵母细胞中tPA水平升高。受精后,妊娠第1 - 4天胚胎中的tPA水平保持较高,但在第5天急剧下降。此外,在垂体切除并植入DES的大鼠中,无论是停用DES还是GnRHa处理后,闭锁卵泡中的卵母细胞tPA水平升高,同时伴有生发泡破裂(GVBD)。免疫组织化学染色显示,tPA抗原仅存在于那些经历明显减数分裂成熟的卵母细胞中,这已通过GVBD得到证实。因此,卵母细胞含有tPA mRNA,并在导致GVBD的各种刺激下合成活性蛋白酶。观察到的卵母细胞tPA活性在排卵期增加、在妊娠第5天之前保持以及tPA在闭锁卵泡的未排卵卵母细胞中的表达,提示卵母细胞和胚胎tPA具有多种功能。