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[腺相关病毒编码融合基因转移后PR39的分泌表达诱导缺氧鸡胚血管生成]

[Secretory expression of PR39 following adeno-associated viral-encoding fusion gene transfer induces angiogenesis in hypoxia chick embryo].

作者信息

Hao Yue-wen, Sun Li-jun, Liu Ying, Wang Quan-ying, Yang Guang-xiao

机构信息

Department of Radiology, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China.

出版信息

Zhonghua Xin Xue Guan Bing Za Zhi. 2009 Aug;37(8):746-9.

Abstract

OBJECTIVES

To investigate the impact of AAV-encoding NT4-TAT-His-PR39 fusion gene expression on HIF-1alpha level in ECV304 cultured under hypoxic condition (1%O(2)) and on angiogenesis in hypoxic chick embryo.

METHODS

PR39 cDNA was connected with NT4, TAT, 6 x His cDNA by molecular biology methods. The recombinant AAV vector was obtained by three plasmid co-transfection in 293 cells. Then ECV304 were respectively infected with AAV-NT4-TAT-His-PR39, 6 x His expression and HIF-1alpha level in ECV304 were detected by immunocytochemistry. The chicken embryos were randomized into the AAV-PR39, EV and PBS groups (n = 10 each) subject to hypoxia (5%O(2), n = 15) or normoxia environments (n = 15), the vessel density of the chicken chorioallantoic membrane (CAM) were measured by Image Pro Plus (IPP) software.

RESULTS

The expression of 6 x His protein was detected in AAV-PR39 infected ECV304 cells. HIF-1alpha protein activity was significantly increased in AAV-PR39 infected ECV304 underwent hypoxia compared to PBS and non-infected ECV304 groups (P < 0.05). The vessel density of chicken CAM in hypoxia environment but not in normoxia environment was also significantly higher in AAV-PR39 group than in EV group and PBS group (all P < 0.05).

CONCLUSION

AAV-encoding NT4-TAT-His-PR39 fusion gene expression significantly increased HIF-1alpha level in ECV304 exposed to hypoxia and promoted angiogenesis in hypoxic chicken embryo.

摘要

目的

研究编码NT4-TAT-His-PR39融合基因的腺相关病毒(AAV)表达对低氧条件(1%O₂)下培养的ECV304细胞中低氧诱导因子-1α(HIF-1α)水平以及对低氧鸡胚血管生成的影响。

方法

采用分子生物学方法将PR39 cDNA与NT4、TAT、6×His cDNA连接。通过三质粒共转染293细胞获得重组AAV载体。然后分别用AAV-NT4-TAT-His-PR39感染ECV304细胞,采用免疫细胞化学法检测ECV304细胞中6×His表达及HIF-1α水平。将鸡胚随机分为AAV-PR39组、空载体(EV)组和磷酸盐缓冲液(PBS)组(每组n = 10),分别置于低氧(5%O₂,n = 15)或常氧环境(n = 15)中,用Image Pro Plus(IPP)软件测量鸡胚绒毛尿囊膜(CAM)的血管密度。

结果

在AAV-PR39感染的ECV304细胞中检测到6×His蛋白表达。与PBS组和未感染的ECV304组相比,低氧处理的AAV-PR39感染的ECV304细胞中HIF-1α蛋白活性显著增加(P < 0.05)。在低氧环境而非常氧环境下,AAV-PR39组鸡胚CAM的血管密度也显著高于EV组和PBS组(均P < 0.05)。

结论

编码NT4-TAT-His-PR39融合基因的AAV表达显著增加了低氧条件下ECV304细胞中的HIF-1α水平,并促进了低氧鸡胚的血管生成。

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