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自身免疫性睾丸炎大鼠生精小管中黏附连接蛋白和缝隙连接蛋白的表达及分布受损。

Impaired expression and distribution of adherens and gap junction proteins in the seminiferous tubules of rats undergoing autoimmune orchitis.

作者信息

Pérez C, Sobarzo C, Jacobo P, Jarazo Dietrich S, Theas M, Denduchis B, Lustig L

机构信息

Instituto de Investigaciones en Reproducción, Facultad de Medicina, Universidad de Buenos Aires, Buenos Aires, Argentina.

出版信息

Int J Androl. 2011 Dec;34(6 Pt 2):e566-77. doi: 10.1111/j.1365-2605.2011.01165.x. Epub 2011 May 25.

DOI:10.1111/j.1365-2605.2011.01165.x
PMID:21615420
Abstract

Experimental autoimmune orchitis (EAO) is characterized by an interstitial lymphomononuclear cell infiltration and a severe lesion of seminiferous tubules (ST) with germ cells that undergo apoptosis and sloughing. The aim of this study was to analyse the expression and localization of adherens junction (AJ) proteins: N-cadherin, α-, β- and p120 catenins and gap junction protein, connexin 43 (Cx43), to explore some aspects of germ-cell sloughing during the development of orchitis. EAO was induced in Sprague-Dawley adult rats by active immunization with testicular homogenate and adjuvants. Control rats (C) were injected with saline solution and adjuvants. Concomitant with early signs of germ-cell sloughing, we observed by immunofluorescence and Western blot, a delocalization and a significant increase in N-cadherin and α-catenin expression in the ST of EAO compared with C rats. In spite of this increased AJ protein expression, a severe germ-cell sloughing occurred. This is probably due to the impairment of the AJ complex function, as shown by the loss of N-cadherin/β-catenin colocalization (confocal microscopy) and increased pY654 β-catenin expression, suggesting lower affinity of these two proteins and increased pERK1/2 expression in the testis of EAO rats. The significant decrease in Cx43 expression detected in EAO rats suggests a gap junction function impairment also contributing to germ-cell sloughing.

摘要

实验性自身免疫性睾丸炎(EAO)的特征是间质淋巴细胞单核细胞浸润以及生精小管(ST)严重受损,生殖细胞发生凋亡和脱落。本研究的目的是分析黏附连接(AJ)蛋白:N-钙黏蛋白、α-、β-连环蛋白和p120连环蛋白以及缝隙连接蛋白连接蛋白43(Cx43)的表达和定位,以探讨睾丸炎发展过程中生殖细胞脱落的一些方面。通过用睾丸匀浆和佐剂对成年Sprague-Dawley大鼠进行主动免疫诱导EAO。对照大鼠(C)注射盐溶液和佐剂。与生殖细胞脱落的早期迹象同时出现的是,通过免疫荧光和蛋白质印迹法观察到,与C组大鼠相比,EAO组大鼠的生精小管中N-钙黏蛋白和α-连环蛋白表达出现异位并显著增加。尽管AJ蛋白表达增加,但仍发生了严重的生殖细胞脱落。这可能是由于AJ复合体功能受损,如N-钙黏蛋白/β-连环蛋白共定位丧失(共聚焦显微镜检查)以及pY654β-连环蛋白表达增加所示,这表明这两种蛋白的亲和力降低,并且EAO组大鼠睾丸中pERK1/2表达增加。在EAO组大鼠中检测到的Cx43表达显著降低表明缝隙连接功能受损也导致了生殖细胞脱落。

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