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[血小板膜受体糖蛋白Ib-IX-V复合物在瞬时转染的人胚肾293T细胞中的异常表达]

[Abnormal expression of the platelet membrane receptor glycoprotein Ib-IX-V complex in transiently transfected HEK 293T cells].

作者信息

Liu Lan-Bo, Mo Qian

机构信息

Institute for Pediatric Translational Medicine, Shanghai Children's Medical Center, Shanghai Jiaotong University School of Medicine, Shanghai 200127, China.

出版信息

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2013 Oct;21(5):1200-6. doi: 10.7534/j.issn.1009-2137.2013.05.023.

Abstract

The structure and function of the glycoprotein (GP) Ib-IX-V complex has been extensively investigated over the decades due to its vital role in platelet activation. For the lack of nucleus in platelets, researchers usually need to study the GPIb-IX-V complex by transfecting wild type or mutant GPIb-IX-V plasmids into other mammalian cell lines, such as CHO or HEK 293T. Therefore, whether the characteristics of the GPIb-IX-V complex in these cell lines can truly represent that in platelets is pivotal to determine whether these cell lines are appropriate for GPIb-IX-V complex studies. In order to determine the most appropriate cell line to study the GPIb-IX-V complex, the surface expression level of the complex in different cell lines was detected and whether difference among cell lines will affect expression of the complex was explored in the present study. The different combinations of the GPIb-IX-V subunits were transfected into cell lines from different species or different tissues, such as CHO, HEK293T and HeLa, and the surface expression levels of the complex were detected by flow cytometry. The results indicated that in both transiently and stably transfected CHO cells, surface expression of GPV depended on the presence of the GPIb-IX complex, which is consistent with that in human platelets. In contrast, GPV could be efficiently expressed on surface in HEK 293T cells even in the absence of GPIb-IX, although the inter-subunit dependence within the GPIb-IX complex is still similar to that in CHO cells or human platelets. Further studies in HeLa, MES13 and HUVEC cell lines revealed that GPV could be efficiently expressed on the surface by itself in HeLa and MES13 cells, but not in HUVEC, suggesting different behaviors of the GPIb-IX-V complex in difference cell lines. It is concluded that this study provides some guidance and advice to future GPIb-IX-V complex studies, especially to the choice of suitable cell line. HEK 293T cell line, for example, is likely to provide misleading results since it could not represent the fact in human platelets, thus is not the optimal choice for the GPIb-IX-V complex, particularly the GPV subunit.

摘要

几十年来,糖蛋白(GP)Ib-IX-V复合物的结构和功能一直受到广泛研究,因为它在血小板激活中起着至关重要的作用。由于血小板中缺乏细胞核,研究人员通常需要通过将野生型或突变型GPIb-IX-V质粒转染到其他哺乳动物细胞系(如CHO或HEK 293T)中来研究GPIb-IX-V复合物。因此,这些细胞系中GPIb-IX-V复合物的特性是否能真正代表血小板中的特性,对于确定这些细胞系是否适合进行GPIb-IX-V复合物研究至关重要。为了确定研究GPIb-IX-V复合物的最合适细胞系,本研究检测了不同细胞系中该复合物的表面表达水平,并探讨了细胞系之间的差异是否会影响该复合物的表达。将GPIb-IX-V亚基的不同组合转染到来自不同物种或不同组织的细胞系中,如CHO、HEK293T和HeLa,并通过流式细胞术检测该复合物的表面表达水平。结果表明,在瞬时和稳定转染的CHO细胞中,GPV的表面表达依赖于GPIb-IX复合物的存在,这与人类血小板中的情况一致。相比之下,即使在没有GPIb-IX的情况下,GPV也能在HEK 293T细胞表面高效表达,尽管GPIb-IX复合物内亚基之间的依赖性仍与CHO细胞或人类血小板中的相似。对HeLa、MES13和HUVEC细胞系的进一步研究表明,GPV在HeLa和MES13细胞中可以自身高效表达于表面,但在HUVEC中则不能,这表明GPIb-IX-V复合物在不同细胞系中的行为不同。结论是,本研究为未来的GPIb-IX-V复合物研究提供了一些指导和建议,特别是在合适细胞系的选择方面。例如,HEK 293T细胞系可能会提供误导性结果,因为它不能代表人类血小板中的实际情况,因此不是研究GPIb-IX-V复合物,特别是GPV亚基的最佳选择。

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