首页> 外文期刊>The American journal of pathology. >Generation of a Novel Transgenic Mouse Model for Bioluminescent Monitoring of Survivin Gene Activity in Vivo at Various Pathophysiological Processes: Survivin Expression Overlaps with Stem Cell Markers
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Generation of a Novel Transgenic Mouse Model for Bioluminescent Monitoring of Survivin Gene Activity in Vivo at Various Pathophysiological Processes: Survivin Expression Overlaps with Stem Cell Markers

机译:在各种病理生理过程中体内存活蛋白基因活性的生物发光监测的新型转基因小鼠模型的产生:具有干细胞标记的存活蛋白表达重叠

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Survival has been implicated to play an important role in various pathophysiological processes. However, because of a lack of appropriate animal models, the role and dynamic expression of survivin during pathophysiology are not well defined. We generated a human survivin gene promoter-driven luciferase transgenic mouse model (SPlucTg) so that dynamic survivin gene activity can be monitored during various pathophysiological conditions using in vivo imaging. Our results show that, consistent with survivin positivity in testis, luciferase activity in normal SPlucTg mice was detected in the testis of male mice. Furthermore, similar to the known requirement of transient expression of survivin for pathophysiological responses, we observed a transient luciferase expression in castrated SPlucTg male mice after supplement of androgen. Significantly, it was reported that survivin expression turns on during mouse liver injury and regeneration; a transient and dose-dependent luciferase expression in the mouse liver was observed after administration of carbon tetrachloride into SPlucTg mice. We further demonstrated that luciferase activity closely correlates with endogenous survivin expression. We also demonstrated that only a subset of cells expresses survivin, and its expression overlaps with the expression of several stem cell markers tested. Thus, we have generated a unique animal model for analysis of diverse pathophysiological processes and possible stem cell distribution/activity in vivo.
机译:已暗示存活在各种病理生理过程中起重要作用。但是,由于缺乏合适的动物模型,在病理生理过程中survivin的作用和动态表达尚不清楚。我们生成了人类生存素基因启动子驱动的荧光素酶转基因小鼠模型(SPlucTg),以便可以在体内使用各种成像生理条件监测动态的生存素基因活性。我们的结果表明,与睾丸中survivin阳性相符,在雄性小鼠的睾丸中检测到了正常SPlucTg小鼠的萤光素酶活性。此外,类似于已知的survivin瞬时表达对于病理生理反应的要求,我们在补充雄激素后观察到cast割的SPlucTg雄性小鼠中的瞬时荧光素酶表达。值得注意的是,据报道在小鼠肝损伤和再生过程中survivin表达开启。向SPlucTg小鼠中施用四氯化碳后,在小鼠肝脏中观察到瞬时和剂量依赖性荧光素酶表达。我们进一步证明,萤光素酶活性与内源性survivin表达密切相关。我们还证明,只有一部分细胞表达survivin,并且其表达与测试的几种干细胞标记物的表达重叠。因此,我们已经生成了独特的动物模型,用于分析多种病理生理过程以及体内可能的干细胞分布/活性。

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