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组织因子途径抑制剂通过调控细胞周期抑制人血管平滑肌细胞的生长。

Tissue factor pathway inhibitor suppresses the growth of human vascular smooth muscle cells through regulating cell cycle.

机构信息

Institute of Biomedical Engineering, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin Key Laboratory of Biomedical Materials, Tianjin 300192, China.

出版信息

Mol Biol Rep. 2011 Oct;38(7):4771-6. doi: 10.1007/s11033-010-0614-0. Epub 2010 Dec 4.

Abstract

Tissue factor pathway inhibitor (TFPI) was reported to suppress the proliferation and migration of vascular smooth muscle cells (VSMCs) which play an important role in several vascular proliferative disorders including restenosis. Our preliminary studies demonstrated that TFPI gene induced apoptosis in human vascular smooth muscle cells (hVSMCs). The current study was designed to address the role TFPI gene plays in the cell cycle of hVSMCs. hVSMCs isolated from human umbilical artery were transfected with pIRES-TFPI plasmid which expresses TFPI in eukaryotic cells. As measured by RT-PCR, the expression of TFPI was elevated in the TFPI treated cells, leading to the arrest of the cells at G1 phase as analyzed by flow cytometry. Further study by Western blotting demonstrated that TFPI gene transfer increased the amount of p21 and p53 and decreased the amount of cyclin D and phosphorylated cdk4 and cdk6 in the cells.

摘要

组织因子途径抑制剂(TFPI)被报道能抑制血管平滑肌细胞(VSMCs)的增殖和迁移,VSMCs 在多种血管增殖性疾病中发挥重要作用,包括再狭窄。我们的初步研究表明 TFPI 基因可诱导人血管平滑肌细胞(hVSMCs)凋亡。本研究旨在探讨 TFPI 基因在 hVSMCs 细胞周期中的作用。用表达 TFPI 的 pIRES-TFPI 质粒转染分离自人脐动脉的 hVSMCs。RT-PCR 检测结果显示,TFPI 处理的细胞中 TFPI 表达升高,导致细胞周期阻滞于 G1 期,流式细胞术分析结果与此一致。进一步的 Western blot 研究表明,TFPI 基因转染增加了 p21 和 p53 的含量,降低了细胞中环化蛋白 D 和磷酸化 CDK4、CDK6 的含量。

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