From the Department of Neurobiology and.
the Core Facility for Electron Microscopy, Max Delbrück Center for Molecular Medicine, Helmholtz Association, D-13092 Berlin, Germany.
J Biol Chem. 2017 Dec 29;292(52):21490-21503. doi: 10.1074/jbc.RA117.000113. Epub 2017 Nov 9.
The Ig-like cell adhesion molecule (IgCAM) BT-IgSF (brain- and testis-specific Ig superfamily protein) plays a major role in male fertility in mice. However, the molecular mechanism by which BT-IgSF supports fertility is unclear. Here, we found that it is localized in Sertoli cells at the blood-testis barrier (BTB) and at the apical ectoplasmic specialization. The absence of BT-IgSF in Sertoli cells in both global and conditional mouse mutants ( AMHCre and Rosa26CreERT2 lines) resulted in male infertility, atrophic testes with vacuolation, azoospermia, and spermatogenesis arrest. Although transcripts of junctional proteins such as connexin43, ZO-1, occludin, and claudin11 were up-regulated in the absence of BT-IgSF, the functional integrity of the BTB was impaired, as revealed by injection of a BTB-impermeable component into the testes under conditions. Disruption of the BTB coincided with mislocalization of connexin43, which was present throughout the seminiferous epithelium and not restricted to the BTB as in wild-type tissues, suggesting impaired cell-cell communication in the BT-IgSF-KO mice. Because EM images revealed a normal BTB structure between Sertoli cells in the BT-IgSF-KO mice, we conclude that infertility in these mice is most likely caused by a functionally impaired BTB. In summary, our results indicate that BT-IgSF is expressed at the BTB and is required for male fertility by supporting the functional integrity of the BTB.
Ig 样细胞黏附分子(IgCAM)BT-IgSF(脑和睾丸特异性 Ig 超家族蛋白)在小鼠的雄性生育力中起着重要作用。然而,BT-IgSF 支持生育力的分子机制尚不清楚。在这里,我们发现它定位于血睾屏障(BTB)和顶外侧质膜特化处的支持细胞中。在全球和条件性小鼠突变体(AMHCre 和 Rosa26CreERT2 系)中,BT-IgSF 在支持细胞中的缺失导致雄性不育、睾丸萎缩伴空泡化、无精子症和精子发生停滞。尽管在没有 BT-IgSF 的情况下,连接蛋白 43、ZO-1、occludin 和 claudin11 等连接蛋白的转录本上调,但 BTB 的功能完整性受损,这是通过在条件下将 BTB 不可渗透的成分注入睾丸中得到证实的。BTB 的破坏伴随着连接蛋白 43 的定位错误,连接蛋白 43 存在于整个生精上皮中,而不是像在野生型组织中那样局限于 BTB,这表明 BT-IgSF-KO 小鼠中的细胞间通讯受损。由于 EM 图像显示 BT-IgSF-KO 小鼠中的支持细胞之间存在正常的 BTB 结构,我们得出结论,这些小鼠的不育很可能是由于 BTB 的功能受损所致。总之,我们的结果表明,BT-IgSF 在 BTB 处表达,并且通过支持 BTB 的功能完整性来维持雄性生育力。