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细胞外基质金属蛋白酶诱导子突变的血管平滑肌细胞的构建及其功能研究

张云燕 林威钢 徐程 张芸 方崇峰

心脑血管病防治2024,Vol.24Issue(4):15-18,23,5.
心脑血管病防治2024,Vol.24Issue(4):15-18,23,5.DOI:10.3969/j.issn.1009-816x.2024.04.004

细胞外基质金属蛋白酶诱导子突变的血管平滑肌细胞的构建及其功能研究

Construction and functional study of vascular smooth muscle cells with extracellular matrix metalloproteinase inducer mutation

张云燕 1林威钢 2徐程 1张芸 1方崇峰1

作者信息

  • 1. 317000 临海,温州医科大学附属台州医院心血管内科
  • 2. 317000 临海,温州医科大学附属台州医院整形科
  • 折叠

摘要

Abstract

Objective To explore the effects of extracellular matrix metalloproteinase inducer(EMMPRIN)on the proliferation,migration and inflammatory response of vascular smooth muscle cells(VSMCs).Methods CRISPR/Cas9 technology was used to construct EMMPRIN c.889C>A-point mutation VSMC line.Real-time qPCR and Western blot were performed to detect the expression level of EMMPRIN.Cell proliferation activity was measured using the CCK-8 assay,while cell migration capability was evaluated using the Transwell assay.Secretion of interleukin-6(IL-6),monocyte chemoattractant protein-1(MCP-1),and interleukin-1β(IL-1β)was detected using enzyme-linked immunosorbent assay(ELISA).Results Compared to the wild-type(WT)cells,the expression level of EMMPRIN did not exhibit significant changes in c.889C>A mutant cells(t=0.732,P>0.05).There was no statistically significant difference in cell proliferation activity(P>0.05),while cell migration capacity significantly decreased(t=5.121,P<0.05).Secretion of inflammatory cytokines IL-6,MCP-1 and IL-1β induced by TGF-β decreased markedly in the c.889C>A mutant cells(t=9.371,5.690,6.192;P<0.05).Conclusion The EMMPRIN c.889C>A mutation does not affect the expression of EMMPRIN or VSMCs proliferation.However,it can supress the migration of VSMCs and the secretion of inflammatory cytokines.

关键词

细胞外基质金属蛋白酶诱导子/血管平滑肌细胞/增殖/迁移

Key words

Extracellular matrix metalloproteinase inducer/Vascular smooth muscle cells/Proliferation/Migration

引用本文复制引用

张云燕,林威钢,徐程,张芸,方崇峰..细胞外基质金属蛋白酶诱导子突变的血管平滑肌细胞的构建及其功能研究[J].心脑血管病防治,2024,24(4):15-18,23,5.

基金项目

浙江省台州市科技计划项目(1801ky13) (1801ky13)

心脑血管病防治

OACSTPCD

1009-816X

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