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首页> 外文期刊>Human and Experimental Toxicology >Immunoexpressions of embryonic and nonembryonic stem cell markers (Nanog, Thy-1, c-kit) and cellular connections (connexin 43 and occludin) on testicular tissue in thyrotoxicosis rat model
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Immunoexpressions of embryonic and nonembryonic stem cell markers (Nanog, Thy-1, c-kit) and cellular connections (connexin 43 and occludin) on testicular tissue in thyrotoxicosis rat model

机译:甲状腺毒症大鼠模型中睾丸组织上胚胎和非胚性干细胞标志物(Nanog,Thy-1,c-kit)的免疫表达和细胞连接(连接蛋白43和occludin)的表达

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In this study, possible thyrotoxicosis-related histological changes in testicular tissues of rats with experimentally induced thyrotoxicosis model were evaluated on cellular connections and stem cell markers. Two experimental groups, thyrotoxicosis and control, each consisting of eight animals were used. Rats in the thyrotoxicosis group were injected intraperitoneally with 3,3,5-triiodo-l-thyronine (50 mu g/100 g body weight/day) for 10 days. At the end of the study, animals in both groups were anesthetized, and blood samples were collected for biochemical analyses. Their testes were dissected out and histological procedure was conducted to perform further histochemical, immunohistochemical analyses and tissue expression analysis by real-time polymerase chain reaction. Expression of the stem cell markers such as c-kit and Thy-1 significantly decreased in the testes of the thyrotoxicosis group compared with the control group; however, Nanog expression was not detected in any of the groups. Similarly, connexin 43 and occludin expressions were also found to be significantly lower in the thyrotoxicosis group. These results on cellular connections are supported with the tissue expression analysis. Our findings are indicative of supporting microenvironmental tissue decay rather than parenchyma damage, which has been actually ignored in the literature. In conclusion, experimental thyrotoxicosis model may have adverse effects on the cell junctional complexes, cell-cell interactions, and pluripotency capacity.
机译:在这项研究中,通过细胞连接和干细胞标志物评估了实验性甲状腺毒症模型大鼠睾丸组织中可能与甲状腺毒症相关的组织学变化。使用两个实验组,甲状腺毒症和对照,每组由八只动物组成。甲状腺毒症组的大鼠腹膜内注射3,3,5-三碘-1-甲状腺素(50μg/ 100 g体重/天),持续10天。在研究结束时,对两组动物进行麻醉,并收集血样进行生化分析。解剖他们的睾丸并进行组织学程序以通过实时聚合酶链反应进一步进行组织化学,免疫组织化学分析和组织表达分析。与对照组相比,在甲状腺毒症组的睾丸中,干细胞标志物(例如c-kit和Thy-1)的表达显着降低;但是,在所有组中均未检测到Nanog表达。类似地,在甲状腺毒症组中也发现连接蛋白43和occludin的表达明显降低。组织表达分析支持细胞连接的这些结果。我们的发现表明支持微环境组织衰变,而不是实质破坏,这在文献中实际上已被忽略。总之,实验性甲状腺毒症模型可能会对细胞连接复合物,细胞间相互作用和多能能力产生不利影响。

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