Fujihara Yoshitaka, Okabe Masaru, Ikawa Masahito
Research Institute for Microbial Diseases, Osaka University, Osaka, Japan.
Biol Reprod. 2014 Mar 20;90(3):60. doi: 10.1095/biolreprod.113.112888. Print 2014 Mar.
A disintegrin and metallopeptidase domain 3 (ADAM3) is a sperm membrane protein reported to be critical for both sperm migration from the uterus into the oviduct in vivo and sperm binding to the zona pellucida in vitro. In order for ADAM3 to be expressed on the sperm surface, the interaction with testis-expressed gene 101 (TEX101), a glycosylphosphatidylinositol (GPI)-anchored protein, is essential. Without TEX101, ADAM3 is degraded during sperm transition through the epididymis. However, it is also known that TEX101 has to be shed and to disappear from testicular germ cells (TGCs) by the GPI-anchored protein-releasing activity of angiotensin-converting enzyme (ACE) for the correct localization of ADAM3 on the mature sperm surface to take place. Here, we found that in a mouse line with a disruption for another testis-specific GPI-anchored protein, lymphocyte antigen 6 complex, locus K (LY6K), the male mice became infertile and demonstrated a phenotype similar to that found in Adam3(-/-), Tex101(-/-), and Ace(-/-) mice. LY6K interacted with TEX101 and ADAM3 in the TGCs but disappeared from mature spermatozoa. Differing from more than 10 previously known gene knockout mouse lines that showed male infertility by impaired sperm migration into the oviduct, spermatozoa from Ly6K(-/-) mice had no aberrance in ADAM3. Thus, LY6K is a newly identified factor involved in sperm fertilizing ability. The lack of effect on ADAM3 in Ly6K(-/-) mice is indicative of an as yet undefined pathway in the mouse.
解整合素金属蛋白酶结构域3(ADAM3)是一种精子膜蛋白,据报道,它对于体内精子从子宫向输卵管的迁移以及体外精子与透明带的结合都至关重要。为了使ADAM3在精子表面表达,与睾丸表达基因101(TEX101)(一种糖基磷脂酰肌醇(GPI)锚定蛋白)的相互作用必不可少。没有TEX101,ADAM3在精子通过附睾的过程中会被降解。然而,也已知TEX101必须通过血管紧张素转换酶(ACE)的GPI锚定蛋白释放活性从睾丸生殖细胞(TGCs)中脱落并消失,才能使ADAM3在成熟精子表面正确定位。在这里,我们发现,在另一种睾丸特异性GPI锚定蛋白淋巴细胞抗原6复合体基因座K(LY6K)缺失的小鼠品系中,雄性小鼠不育,表现出与Adam3(-/-)、Tex101(-/-)和Ace(-/-)小鼠相似的表型。LY6K在TGCs中与TEX101和ADAM3相互作用,但在成熟精子中消失。与之前已知的10多个因精子向输卵管迁移受损而导致雄性不育的基因敲除小鼠品系不同,Ly6K(-/-)小鼠的精子中ADAM3没有异常。因此,LY6K是一个新发现的参与精子受精能力的因素。Ly6K(-/-)小鼠对ADAM3没有影响,这表明小鼠中存在一条尚未明确的途径。