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p38丝裂原活化蛋白激酶和诱导型一氧化氮合酶参与激素剥夺后小鼠和人类雄性生殖细胞的凋亡信号传导。

Involvement of p38 mitogen-activated protein kinase and inducible nitric oxide synthase in apoptotic signaling of murine and human male germ cells after hormone deprivation.

作者信息

Vera Yanira, Erkkilä Krista, Wang Christina, Nunez Concepcion, Kyttänen Sauli, Lue Yanhe, Dunkel Leo, Swerdloff Ronald S, Sinha Hikim Amiya P

机构信息

Division of Endocrinology, Harbor-University of California at Los Angeles Medical Center, Los Angeles Biomedical Research Institute, Torrance, California 90509, USA.

出版信息

Mol Endocrinol. 2006 Jul;20(7):1597-609. doi: 10.1210/me.2005-0395. Epub 2006 Feb 9.

DOI:10.1210/me.2005-0395
PMID:16469770
Abstract

This study investigates the role of p38 MAPK, inducible nitric oxide synthase (iNOS), and the intrinsic pathway signaling in male germ cell death in rats after hormonal deprivation by a potent GnRH antagonist treatment. Germ cell apoptosis, involving exclusively middle (VII-VIII) stages, was activated by d 5 after GnRH antagonist treatment. Initiation of germ cell apoptosis was preceded by p38 MAPK activation and induction of iNOS. p38 MAPK activation and iNOS induction were further accompanied by a marked perturbation of the BAX/BCL-2 rheostat, cytochrome c, and DIABLO release from mitochondria, caspase activation, and poly(ADP-ribose) polymerase cleavage. Concomitant administration of aminoguanidine, a selective iNOS inhibitor, significantly prevented hormone deprivation-induced germ cell apoptosis. Inhibitors of iNOS or p38 MAPK were also effective in preventing human male germ cell apoptosis induced by hormone-free culture conditions. Together, these results establish a new signal transduction pathway involving p38 MAPK and iNOS that, through activation of the intrinsic pathway signaling, promotes male germ cell death in response to a lack of hormonal stimulation across species.

摘要

本研究通过强效促性腺激素释放激素(GnRH)拮抗剂处理,调查了p38丝裂原活化蛋白激酶(MAPK)、诱导型一氧化氮合酶(iNOS)以及内在信号通路在大鼠激素剥夺后雄性生殖细胞死亡中的作用。仅涉及中期(VII - VIII期)的生殖细胞凋亡在GnRH拮抗剂处理后第5天被激活。生殖细胞凋亡的起始先于p38 MAPK的激活和iNOS的诱导。p38 MAPK的激活和iNOS的诱导还伴随着BAX/BCL - 2平衡、细胞色素c以及线粒体中DIABLO的释放、半胱天冬酶激活和聚(ADP - 核糖)聚合酶裂解的显著扰动。同时给予选择性iNOS抑制剂氨基胍可显著预防激素剥夺诱导的生殖细胞凋亡。iNOS或p38 MAPK的抑制剂在预防无激素培养条件诱导的人类雄性生殖细胞凋亡方面也有效。总之,这些结果建立了一条涉及p38 MAPK和iNOS的新信号转导途径,该途径通过激活内在信号通路,促进跨物种对激素刺激缺乏的反应中雄性生殖细胞的死亡。

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