Structural Alterations of Epididymal Epithelial Cells in Cathepsin A—Deficient Mice Affect the Blood-Epididymal Barrier and Lead to Altered Sperm Motility

Louis Hermo, Nadine Korah, Mary Gregory, Lauren Ye Liu, Daniel G. Cyr, Alessandra D'Azzo, Charles E. Smith
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引用次数: 26

Abstract

ABSTRACT: Past studies have shown that the epithelial lining of the epididymis in adult mice deficient in protective protein cathepsin A (PPCA −/−) becomes swollen and vacuolated as a result of an accumulation of pale lysosomes, some very large, in addition to the presence of an abundance of macrophages infiltrating the intertubular spaces. The purpose of this study was to assess the integrity of the epididymal epithelial—blood barrier in these altered mice by characterizing the distribution of claudins (Cldns) and the leakiness of tight junctions to lanthanum nitrate. A second goal was to characterize sperm motility behavior in PPCA −/− mice using computer-assisted sperm analyses (CASA). The results indicated that lanthanum nitrate penetrated apical junctional complexes between adjacent epithelial cells and entered the epididymal lumen in PPCA −/− mice but not in control PPCA +/+ mice. Immunostaining for Cldns 1, 3, 8, and 10 revealed unique patterns of expression based on cell type and region specificity in PPCA +/+ mice, which were much different in PPCA –/– mice. PPCA –/– mice showed reduced intensities of immunoreactions, complete absence of immunoreactions, and appearance of atypical cytoplasmic immunoreactions. CASA indicated that sperm counts in the PPCA –/– mice were 70% reduced, and among other problems, there was a fourfold higher percentage of static sperm in PPCA –/– mice compared with controls. These results suggest that PPCA deficiency causes structural changes to the blood-epididymal barrier as evidenced by lanthanum nitrate and Cldns expression that affects the luminal environment of the epididymis, resulting in altered sperm motility.

Abstract Image

组织蛋白酶a缺陷小鼠附睾上皮细胞结构改变影响血-附睾屏障并导致精子活力改变
摘要:过去的研究表明,缺乏保护蛋白组织蛋白酶A (PPCA - / -)的成年小鼠的附睾上皮内壁肿胀和空泡化,这是由于苍白溶酶体的积累,其中一些非常大,此外还有大量巨噬细胞浸润管间间隙。本研究的目的是通过表征Cldns的分布和紧密连接对硝酸镧的泄漏来评估这些改变小鼠附睾上皮-血液屏障的完整性。第二个目标是使用计算机辅助精子分析(CASA)来表征PPCA - / -小鼠的精子运动行为。结果表明,硝酸镧在PPCA−/−小鼠中可穿透相邻上皮细胞间的顶端连接复合物进入附睾管腔,而在对照PPCA +/+小鼠中则没有。在PPCA +/+小鼠中,cldn1、3、8和10的免疫染色显示出基于细胞类型和区域特异性的独特表达模式,而在PPCA - / -小鼠中则有很大不同。PPCA - / -小鼠表现出免疫反应强度降低,完全不存在免疫反应,出现非典型胞质免疫反应。CASA表明,PPCA - / -小鼠的精子数量减少了70%,在其他问题中,PPCA - / -小鼠的静态精子百分比比对照组高4倍。这些结果表明,PPCA缺乏会导致血附睾屏障的结构改变,硝酸镧和Cldns的表达会影响附睾的腔内环境,导致精子活力改变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of andrology
Journal of andrology 医学-男科学
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5.6 months
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