Park Hyun-Jung, Lee Won-Young, Park Chankyu, Hong Kwon-Ho, Kim Jin-Hoi, Song Hyuk
Department of Stem Cell and Regenerative Technology, Konkuk University, Gwangjin-gu, Seoul, Republic of Korea.
Department of Beef and Dairy Science, Korea National College of Agricultures and Fisheries, Jeonju-si 54874, Republic of Korea.
Theriogenology. 2018 Apr 1;110:158-167. doi: 10.1016/j.theriogenology.2018.01.007. Epub 2018 Feb 2.
Whereas stage-specific markers for spermatogonial cells have been well investigated in mouse, the specific markers of germ cells in the testis of domestic animals have not been well defined. Phosphoglycerate kinase (PGK), an enzyme that converts 1,3-bisphosphoglycerate and adenosine diphosphate to 3-phosphoglycerate and adenosine triphosphate, has two isozymes: PGK1 and PGK2. In mouse, PGK1 exists only during the early stages of spermatogenesis, and PGK2 is then expressed during the pachytene spermatocyte stage. In this study, we investigated the localization of PGK2 in the developing porcine testis, and compared the similarities and differences in its expression with that of the PGK2 in mouse. The PGK2 protein was found to be exclusively expressed in spermatids of the adult mouse testis, whereas PGK2-positive cells were observed in the prepubertal and postpubertal testes of pigs. Based on this result, we examined the expression of PGK2 in in vitro-cultured porcine undifferentiated spermatogonia and found it to be maintained in the cultured cells. To verify this result and identify the spermatogonial stem cell-like potential in recipient testes, PKH26 dye-stained PGK2-positive cells were transplanted into the testes of busulfan-treated immunodeficient mouse that had been depleted of both testicular germ cells and somatic cells. The transplanted cells colonized the recipient testis at 8 weeks post transplantation, and fluorescence microscopy identified the cells in the basement membranes of the seminiferous tubules of the injected mouse. Taken together, our results suggest that PGK2 is expressed differently in the testes of mouse and pigs according to developmental stage. This finding should contribute to the study of spermatogenesis and the production of transgenic domestic animals through in vitro spermatogonial sperm cell culture.
尽管在小鼠中对精原细胞的阶段特异性标志物已经进行了充分研究,但家畜睾丸中生殖细胞的特异性标志物尚未明确界定。磷酸甘油酸激酶(PGK)是一种将1,3-二磷酸甘油酸和二磷酸腺苷转化为3-磷酸甘油酸和三磷酸腺苷的酶,有两种同工酶:PGK1和PGK2。在小鼠中,PGK1仅在精子发生的早期阶段存在,然后PGK2在粗线期精母细胞阶段表达。在本研究中,我们研究了PGK2在发育中的猪睾丸中的定位,并比较了其与小鼠PGK2表达的异同。发现PGK2蛋白仅在成年小鼠睾丸的精子细胞中表达,而在猪的青春期前和青春期后睾丸中观察到PGK2阳性细胞。基于这一结果,我们检测了体外培养的猪未分化精原细胞中PGK2的表达,发现其在培养细胞中得以维持。为了验证这一结果并确定受体睾丸中类似精原干细胞的潜能,将PKH26染料染色的PGK2阳性细胞移植到经白消安处理的免疫缺陷小鼠的睾丸中,该小鼠的睾丸生殖细胞和体细胞均已耗尽。移植后第8周,移植细胞在受体睾丸中定植,荧光显微镜在注射小鼠的曲细精管基底膜中鉴定出这些细胞。综上所述,我们的结果表明,PGK2在小鼠和猪的睾丸中根据发育阶段表达不同。这一发现应有助于精子发生的研究以及通过体外精原细胞精子培养生产转基因家畜。