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uroplakin 1a基因敲除小鼠的生育力略有下降,细菌清除能力降低,睾丸转录组发生剧烈变化。

Uroplakin 1a Knockout Mice Display Marginal Reduction in Fecundity, Decreased Bacterial Clearance Capacity, and Drastic Changes in the Testicular Transcriptome.

作者信息

Munipalli Suresh Babu, Yenugu Suresh

机构信息

Department of Animal Biology, University of Hyderabad, Hyderabad, 500046, India.

出版信息

Reprod Sci. 2023 Mar;30(3):914-927. doi: 10.1007/s43032-022-01057-z. Epub 2022 Aug 30.

DOI:10.1007/s43032-022-01057-z
PMID:36042152
Abstract

Uroplakins (UPKs) form physical and chemical barriers in the bladder and other urinary tract tissues. We previously reported the identification and localization of UPKs in the male reproductive tract of rat. In this study, we characterized Upk1a knockout mice and report a marginal reduction in fecundity associated with significant decrease in sperm count. Upk1a mice had lower bacterial clearance capacity when challenged with uropathogenic Escherichia coli for 1 to 5 days. High-throughput analyses of testicular transcriptome indicated that 1128 genes that are expressed in testis of wild-type mice were completely absent in the knockout, while 2330 genes were found to be expressed only in the testis of knockout mice. Furthermore, differential regulation of 148 (67 upregulated and 81 downregulated) was observed. Gene ontology analyses indicated that processes related to integral components of membrane (plasma membrane), G-protein receptor activity and signaling, olfactory receptor activity and perception of smell, organization of extracellular space/region, immune and inflammatory responses to pathogens, spermatid development, meiotic cell cycle, and formation of synaptonemal complex were affected. Results of this study provide evidence on the possible multi-functional role of Upk1a in male reproductive tract and in other tissues as well.

摘要

尿血小板溶素(UPKs)在膀胱和其他泌尿系统组织中形成物理和化学屏障。我们之前报道了尿血小板溶素在大鼠雄性生殖道中的鉴定和定位。在本研究中,我们对Upk1a基因敲除小鼠进行了表征,并报告了其生育力略有下降,同时精子数量显著减少。当用尿路致病性大肠杆菌攻击1至5天时,Upk1a基因敲除小鼠的细菌清除能力较低。睾丸转录组的高通量分析表明,野生型小鼠睾丸中表达的1128个基因在基因敲除小鼠中完全缺失,而2330个基因仅在基因敲除小鼠的睾丸中表达。此外,观察到148个基因(67个上调和81个下调)的差异调节。基因本体分析表明,与膜(质膜)的整合成分、G蛋白受体活性和信号传导、嗅觉受体活性和嗅觉感知、细胞外空间/区域的组织、对病原体的免疫和炎症反应、精子细胞发育、减数分裂细胞周期以及联会复合体形成相关的过程受到影响。本研究结果为Upk1a在雄性生殖道和其他组织中可能具有的多功能作用提供了证据。

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