Yamamoto Yuri, Kuwahara Akira, Taniguchi Yuka, Yamasaki Mikio, Tanaka Yu, Mukai Yukari, Yamashita Mizuho, Matsuzaki Toshiya, Yasui Toshiyuki, Irahara Minoru
Department of Obstetrics and Gynecology, The University of Tokushima, Institute for Health Biosciences, 3-18-15 Kuramoto-cho, Tokushima, 770-8503 Japan.
Reprod Med Biol. 2015;14(3):107-115. doi: 10.1007/s12522-014-0201-5. Epub 2014 Dec 13.
We evaluated the role of tumor necrosis factor alpha (TNFα) in rat ovulation and granulosa cell death of ovarian follicles during the periovulatory stage.
Immature rats primed with pregnant mare serum gonadotropin were injected intraperitoneally with human chorionic gonadotropin (hCG), and TNFα was injected into the bursa 48 h later. The total number of released oocytes was counted. Apoptosis was measured with terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) and the expression of cleaved caspase 3 and Bax/Bcl-2. Autophagy was assessed by the expression of light chain protein 3 (LC3) and autophagosomes under transmission electron microscopy.
TNFα significantly decreased the number of released oocytes, and many unruptured follicles were observed. TUNEL analysis revealed a larger number of apoptotic cells, and the cleaved caspase 3 and Bax/Bcl-2 increased more than that of the control 12 h after hCG administration. Furthermore, the expression of LC3 wwas significantly higher than that of the control, and autophagosomes were observed in the cytoplasm.
Our data indicated that TNFα is an important mediator of ovulation in terms of decreasing the number of released oocytes and inducing granulosa cell death of unruptured follicles via apoptosis and autophagy for remodeling ovarian tissues.
我们评估了肿瘤坏死因子α(TNFα)在大鼠排卵以及围排卵期卵巢卵泡颗粒细胞死亡过程中的作用。
用孕马血清促性腺激素预处理的未成熟大鼠腹腔注射人绒毛膜促性腺激素(hCG),48小时后将TNFα注射到囊腔中。计算排出的卵母细胞总数。采用末端脱氧核苷酸转移酶介导的dUTP缺口末端标记法(TUNEL)检测细胞凋亡,并检测裂解的半胱天冬酶3以及Bax/Bcl-2的表达。通过轻链蛋白3(LC3)的表达以及透射电子显微镜下自噬体的观察来评估自噬。
TNFα显著降低了排出的卵母细胞数量,并且观察到许多未破裂的卵泡。TUNEL分析显示凋亡细胞数量更多,在给予hCG 12小时后,裂解的半胱天冬酶3以及Bax/Bcl-2的增加幅度大于对照组。此外,LC3的表达显著高于对照组,并且在细胞质中观察到了自噬体。
我们的数据表明,TNFα是排卵的重要调节因子,它通过诱导未破裂卵泡的颗粒细胞凋亡和自噬来减少排出的卵母细胞数量并重塑卵巢组织。