Ye Xiaoqin, Skinner Michael K, Kennedy Grace, Chun Jerold
Department of Molecular Biology, The Helen L. Dorris Child and Adolescent Neuropsychiatric Disorder Institute, The Scripps Research Institute, La Jolla, California 92037, USA.
Biol Reprod. 2008 Aug;79(2):328-36. doi: 10.1095/biolreprod.108.068783. Epub 2008 Apr 30.
Approximately half of all infertility cases can be attributed to male reproductive dysfunction for which low sperm count is a major contributing factor. The current study identified receptor-mediated lysophosphatidic acid (LPA) signaling as a new molecular component influencing male fertility. LPA is a small signaling phospholipid, the effects of which are mediated through at least five G protein-coupled receptors, named LPA 1-5. LPA1/2/3, but not LPA4/5, show high expression in mouse testis. Mice deficient in LPA1/2/3 showed a testosterone-independent reduction of mating activity and sperm production, with an increased prevalence of azoospermia in aging animals. A significant increase of germ cell apoptosis also was observed in testes. Germ cell apoptosis led to a reduction in germ cell proliferation. These data demonstrate a novel in vivo function for LPA signaling as a germ cell survival factor during spermatogenesis.
大约一半的不孕病例可归因于男性生殖功能障碍,而精子数量少是一个主要因素。当前研究确定受体介导的溶血磷脂酸(LPA)信号传导是影响男性生育能力的一个新的分子成分。LPA是一种小的信号磷脂,其作用通过至少五种G蛋白偶联受体介导,命名为LPA 1-5。LPA1/2/3在小鼠睾丸中高表达,而LPA4/5则不然。缺乏LPA1/2/3的小鼠表现出与睾酮无关的交配活动和精子产生减少,老龄动物无精子症的患病率增加。在睾丸中也观察到生殖细胞凋亡显著增加。生殖细胞凋亡导致生殖细胞增殖减少。这些数据证明LPA信号传导在精子发生过程中作为生殖细胞存活因子具有新的体内功能。