首页> 外文期刊>Journal of Zhejiang University. Science >Immortalization of human umbilical vein endothelial cells with telomerase reverse transcriptase and simian virus 40 large T antigen
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Immortalization of human umbilical vein endothelial cells with telomerase reverse transcriptase and simian virus 40 large T antigen

机译:端粒酶逆转录酶和猿猴病毒40大T抗原使人脐静脉内皮细胞永生化

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Objective: To establish normally conditionally-immortalized human umbilical vein endothelial cells (HUVECs) by ectopic expression of the human telomerase catalytic enzyme (hTERT) and simian virus 40 large T (SV40 LT) antigen. Methods: Primary HUVECs were transfected with recombinant retrovirus containing hTERT or SV40 irrespectively. Subsequently drug resistant cell clones were screened and expanded for further studies. Endothelial cell biomarkers were confirmed by examination. Results: The morphological phenotype of the transfected cells was similar to the non-transfected cells. Von Willebrand factor, hTERT and SV40 LT could be detected in transfected HUVECs. Moreover, higher telomerase activity in transfected cells was maintained for over 50 population doublings compared with only low level of endogenous telomerase transiently at early population doublings in primary HUVECs. When exposed to TNF-α (tumor necrosis factor-α), the expression of E-selectin in transfected cells was significantly up-regulated, but no alteration of endothelial lipase was found. Conclusion: Ectopic coexpression of hTERT and SV40 LT can effectively immortalize HUVECs without tumorigenicity in vitro. Immortalized HUVECs may be an ideal target of further molecular function studies.
机译:目的:通过异位表达人类端粒酶催化酶(hTERT)和猿猴病毒40大T(SV40 LT)抗原,建立正常条件下永生的人脐静脉内皮细胞(HUVEC)。方法:分别用含有hTERT或SV40的重组逆转录病毒转染原代HUVEC。随后筛选抗药性细胞克隆并扩展用于进一步研究。通过检查证实了内皮细胞生物标志物。结果:转染细胞的形态表型与未转染细胞相似。在转染的HUVECs中可以检测到Von Willebrand因子,hTERT和SV40 LT。此外,与原代HUVEC中早期群体倍增时短暂的内源性端粒酶瞬时低水平相比,转染细胞中的端粒酶活性维持了50倍以上。当暴露于TNF-α(肿瘤坏死因子-α)时,E-选择素在转染细胞中的表达显着上调,但未发现内皮脂肪酶的改变。结论:hTERT和SV40 LT的异位共表达可以有效地使HUVEC永生,而无致癌性。永生化的HUVEC可能是进一步分子功能研究的理想目标。

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