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[人血管生成抑制剂血管抑素在昆虫细胞中的表达及生物学活性]

[Expression and biological activity of human angiogenesis inhibitor angiostatin in insect cells].

作者信息

Xu Xiao-Lin, Liu Ge-Fei, Huang Dong-Yang

机构信息

Liaoyang School of Chinese Traditional Medicine, Liaoyang, Liaoning, P.R. China.

出版信息

Ai Zheng. 2005 Sep;24(9):1096-101.

Abstract

BACKGROUND & OBJECTIVE: Angiogenesis is the essential process for tumor growth and metastasis. Angiostatin, a potent endogenous inhibitor of angiogenesis, could selectively inhibit proliferation of vascular endothelial cells. This study was to construct recombinant angiostatin-baculovirus, and explore the expression and biological activity of recombinant angiostatin in insect cells.

METHODS

The angiostatin baculovirus transfer vector pBlueBacHis2B was co-transfected with virus DNA into insect Sf9 cells to construct recombinant baculovirus. The recombinant virus was screened by plaque assay, and confirmed and amplified by polymerase chain reaction (PCR) to produce large scale, high-titer virus stock. The expression of the recombinant protein at different time points was detected by SDS-PAGE and Western blot. The recombinant protein was purified by ProBond purification system. Inhibitory effect of recombinant angiostatin on human umbilical vein endothelial cells (HUVECs) was examined by MTT assay. Its anti-angiogenesis effect was confirmed by in vivo chorioallantoic membrane (CAM) test.

RESULTS

Recombinant angiostatin baculovirus with a high virus titer (2 x 10(8) pfu/ml) was constructed successfully. Recombinant angiostatin (53 ku) was effectively expressed in Sf9 cells, and its pure degree was about 90% of insect cellular total soluble proteins. The recombinant angiostatin obviously inhibited proliferation of endothelial cells with the 50% inhibitory concentration (IC(50)) of 2.3 microg/ml, and remarkably inhibited the growth of vessels in CAM.

CONCLUSIONS

The baculovirus expression system could be used to construct high-titer recombinant angiostatin-virus stock, and highly express the recombinant angiostatin in insect cells. In vitro and in vivo experiments confirmed that angiostatin could inhibit proliferation of vascular endothelial cells.

摘要

背景与目的

血管生成是肿瘤生长和转移的关键过程。血管抑素是一种有效的内源性血管生成抑制剂,可选择性抑制血管内皮细胞的增殖。本研究旨在构建重组血管抑素-杆状病毒,并探讨重组血管抑素在昆虫细胞中的表达及生物学活性。

方法

将血管抑素杆状病毒转移载体pBlueBacHis2B与病毒DNA共转染至昆虫Sf9细胞中构建重组杆状病毒。通过噬斑试验筛选重组病毒,并经聚合酶链反应(PCR)进行鉴定和扩增,以制备大规模、高滴度的病毒储备液。采用十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)和蛋白质免疫印迹法(Western blot)检测不同时间点重组蛋白的表达情况。用ProBond纯化系统对重组蛋白进行纯化。采用MTT法检测重组血管抑素对人脐静脉内皮细胞(HUVECs)的抑制作用。通过鸡胚绒毛尿囊膜(CAM)试验在体内验证其抗血管生成作用。

结果

成功构建了高滴度(2×10⁸ pfu/ml)的重组血管抑素杆状病毒。重组血管抑素(53 ku)在Sf9细胞中有效表达,其纯度约占昆虫细胞总可溶性蛋白的90%。重组血管抑素明显抑制内皮细胞增殖,半数抑制浓度(IC₅₀)为2.3 μg/ml,并显著抑制CAM中血管的生长。

结论

杆状病毒表达系统可用于构建高滴度的重组血管抑素病毒储备液,并在昆虫细胞中高效表达重组血管抑素。体外和体内实验证实血管抑素可抑制血管内皮细胞的增殖。

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