Shimada Keisuke, Kato Hirotaka, Miyata Haruhiko, Ikawa Masahito
Research Institute for Microbial Diseases, Osaka University, Osaka 565-0871, Japan.
The Institute of Medical Science, The University of Tokyo, Tokyo 108-8639, Japan.
J Reprod Dev. 2019 Apr 12;65(2):155-162. doi: 10.1262/jrd.2018-136. Epub 2019 Jan 21.
The mitochondrial sheath is composed of mitochondria that coil tightly around the midpiece of sperm flagellum. These mitochondria are recruited from the cytoplasm to the flagellum late in spermatogenesis. Initially, recruited mitochondria are spherical-shaped but then elongate laterally to become crescent-like in shape. Subsequently, crescent-like mitochondria elongate continuously to coil tightly around the flagellum. Recently, disorganization of the mitochondrial sheath was reported in Glycerol kinase 2 (Gk2) disrupted mice. To analyze the disorganization of the mitochondrial sheath further, we generated Gk2-deficient mice using the CRISPR/Cas9 system and observed sperm mitochondria in testis using a freeze-fracture method with scanning electron microscopy. Gk2-disrupted spermatids show abnormal localization of crescent-like mitochondria, in spite of the initial proper alignment of spherical mitochondria around the flagellum, which causes abnormal mitochondrial sheath formation leading to exposure of the outer dense fibers. These results indicate that GK2 is essential for proper arrangement of crescent-like mitochondria to form the mitochondrial sheath during mouse spermatogenesis.
线粒体鞘由紧密缠绕在精子鞭毛中段的线粒体组成。这些线粒体在精子发生后期从细胞质募集到鞭毛。最初,募集的线粒体呈球形,但随后横向伸长,变成月牙形。随后,月牙形线粒体持续伸长,紧密缠绕在鞭毛周围。最近,在甘油激酶2(Gk2)基因敲除小鼠中报道了线粒体鞘的紊乱。为了进一步分析线粒体鞘的紊乱情况,我们使用CRISPR/Cas9系统构建了Gk2基因敲除小鼠,并采用冷冻断裂扫描电子显微镜观察睾丸中的精子线粒体。尽管球形线粒体最初在鞭毛周围排列正常,但Gk2基因敲除的精子细胞显示月牙形线粒体定位异常,这导致线粒体鞘形成异常,进而导致外致密纤维暴露。这些结果表明,GK2对于小鼠精子发生过程中月牙形线粒体正确排列以形成线粒体鞘至关重要。