Wong Joanne, Juma Almas R, Tran Stephanie C, Gasperoni Jemma G, Grommen Sylvia V H, De Groef Bert
Department of Physiology, Anatomy and Microbiology, La Trobe University, Bundoora, Victoria 3086, Australia.
Asian J Androl. 2020 Jul-Aug;22(4):342-347. doi: 10.4103/aja.aja_87_19.
Mice deficient in the transcription factor pleomorphic adenoma gene 1 (PLAG1) exhibit reproductive issues that are characterized, in part, by decreased progressive sperm motility in the male. However, the underlying cause of this impairment is unknown. As epididymal transit is critical for sperm maturation and motility, the morphology of the epididymis of Plag1-deficient mice was investigated and the spatial expression patterns of PLAG1 protein and mRNA were identified. Using X-gal staining and in situ hybridization, PLAG1 was shown to be widely expressed in both the epithelium and stroma in all regions of the mouse epididymis. Interestingly, the X-gal staining pattern was markedly different in the cauda, where it could be suggestive of PLAG1 secretion into the epididymal lumen. At all ages investigated, the morphology of epididymides from Plag1 knockout (KO) mice was aberrant; the tubule failed to elongate and coil, particularly in the corpus and cauda, and the cauda was malformed, lacking its usual bulbous shape. Moreover, the epididymides from Plag1 KO mice were significantly reduced in size relative to body weight. In 20% of Plag1-deficient mice, the left testicle and epididymis were lacking. The impaired morphogenesis of the epididymal tubule is likely to be a major contributing factor to the fertility problems observed in male Plag1-deficient mice. These results also establish PLAG1 as an important regulator of male reproduction, not only through its involvement in testicular sperm production, but also via its role in the development and function of the epididymis.
转录因子多形性腺瘤基因1(PLAG1)缺陷的小鼠表现出生殖问题,部分特征是雄性小鼠的渐进性精子活力下降。然而,这种损伤的根本原因尚不清楚。由于附睾转运对精子成熟和活力至关重要,因此研究了PLAG1缺陷小鼠附睾的形态,并确定了PLAG1蛋白和mRNA的空间表达模式。通过X-gal染色和原位杂交,发现PLAG1在小鼠附睾所有区域的上皮和基质中均广泛表达。有趣的是,X-gal染色模式在附睾尾部明显不同,这可能暗示PLAG1分泌到附睾管腔中。在所有研究的年龄段,PLAG1基因敲除(KO)小鼠的附睾形态均异常;小管未能伸长和盘绕,特别是在附睾体和尾部,尾部畸形,缺乏其通常的球状形状。此外,PLAG1基因敲除小鼠的附睾相对于体重明显变小。在20%的PLAG1缺陷小鼠中,左侧睾丸和附睾缺失。附睾管形态发生受损可能是PLAG1缺陷雄性小鼠生育问题的主要促成因素。这些结果还确立了PLAG1作为雄性生殖的重要调节因子,不仅通过其参与睾丸精子生成,还通过其在附睾发育和功能中的作用。