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BXSB/MpJ-Yaa mouse model of systemic autoimmune disease shows increased apoptotic germ cells in stage XII of the seminiferous epithelial cycle
Cell and Tissue Research ( IF 3.6 ) Pub Date : 2020-04-04 , DOI: 10.1007/s00441-020-03190-0
Yuki Otani 1 , Osamu Ichii 1, 2 , Md Abdul Masum 1 , Junpei Kimura 1 , Teppei Nakamura 1, 3 , Yaser Hosny Ali Elewa 1, 4 , Yasuhiro Kon 1
Affiliation  

In mammals, the reproductive system and autoimmunity regulate mutual functions. Importantly, systemic autoimmune diseases are thought to cause male infertility but the underlying pathological mechanism remains unclear. In this study, the morpho-function of the testes in BXSB/MpJ-Yaa mice was analyzed as a representative mouse model for systemic autoimmune diseases to investigate the effect of excessive autoimmunity on spermatogenesis. At 12 and 24 weeks of age, BXSB/MpJ-Yaa mice showed splenomegaly and increased levels of serum autoantibodies, whereas no controls showed a similar autoimmune condition. In histological analysis, the enlarged lumen of the seminiferous tubules accompanied with scarce spermatozoa in the epididymal ducts were observed in some of the BXSB/MpJ-Yaa and BXSB/MpJ mice but not in C57BL/6N mice. Histoplanimetrical analysis revealed significantly increased residual bodies and apoptotic germ cells in the seminiferous tubules in BXSB/MpJ-Yaa testes without apparent inflammation. Notably, in stage XII of the seminiferous epithelial cycles, the apoptotic germ cell number was remarkably increased, showing a significant correlation with the indices of systemic autoimmune disease in BXSB/MpJ-Yaa mice. Furthermore, the Sertoli cell number was reduced at the early disease stage, which likely caused subsequent morphological changes in BXSB/MpJ-Yaa testes. Thus, our histological study revealed the altered morphologies of BXSB/MpJ-Yaa testes, which were not observed in controls and statistical analysis suggested the effects of an autoimmune condition on this phenotype, particularly the apoptosis of meiotic germ cells. BXSB/MpJ-Yaa mice were shown to be an efficient model to study the relationship between systemic autoimmune disease and the local reproductive system.

中文翻译:

BXSB/MpJ-Yaa 系统性自身免疫性疾病小鼠模型显示生精上皮周期 XII 期凋亡生殖细胞增加

在哺乳动物中,生殖系统和自身免疫调节相互的功能。重要的是,系统性自身免疫性疾病被认为会导致男性不育,但潜在的病理机制尚不清楚。在这项研究中,分析了 BXSB/MpJ-Yaa 小鼠睾丸的形态功能,作为系统性自身免疫性疾病的代表性小鼠模型,以研究过度自身免疫对精子发生的影响。在 12 和 24 周龄时,BXSB/MpJ-Yaa 小鼠表现出脾肿大和血清自身抗体水平升高,而没有对照组表现出类似的自身免疫状况。在组织学分析中,在一些 BXSB/MpJ-Yaa 和 BXSB/MpJ 小鼠中观察到生精小管腔增大,附睾管中精子稀少,但在 C57BL/6N 小鼠中未观察到。组织学分析显示 BXSB/MpJ-Yaa 睾丸生精小管中残留的小体和凋亡的生殖细胞显着增加,没有明显的炎症。值得注意的是,在生精上皮周期的 XII 阶段,凋亡的生殖细胞数量显着增加,与 BXSB/MpJ-Yaa 小鼠的全身性自身免疫性疾病指标显着相关。此外,在疾病早期,支持细胞数量减少,这可能导致 BXSB/MpJ-Yaa 睾丸随后的形态变化。因此,我们的组织学研究揭示了 BXSB/MpJ-Yaa 睾丸的形态改变,这在对照中未观察到,统计分析表明自身免疫状况对这种表型的影响,特别是减数分裂生殖细胞的凋亡。
更新日期:2020-04-04
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