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肺炎衣原体感染人内皮细胞后 Toll 样受体 2/4 诱导血管内皮生长因子和基质金属蛋白酶-9 的表达。

Induction of VEGF and MMP-9 expression by toll-like receptor 2/4 in human endothelial cells infected with Chlamydia pneumoniae.

机构信息

Department of Experimental Medicine, Section of Microbiology and Clinical Microbiology, Faculty of Medicine and Surgery, Second University of Naples, Naples, Italy.

出版信息

Int J Immunopathol Pharmacol. 2012 Apr-Jun;25(2):377-86. doi: 10.1177/039463201202500207.

Abstract

Matrix metalloproteinases (MMP) are a family of host-derived enzymes involved in the turnover of extracellular matrix (ECM) molecules, and, in particular, it is demonstrated that the 92 KDa gelatinase MMP-9 is often expressed in atherosclerotic plaques by macrophages and smooth muscle cells. Recent evidence supports a role of Toll-like receptor (TLR) signaling in the development of atherosclerosis lesions. In this study, we analyzed the TLR2/TLR4 expression in HUVEC infected with C. pneumoniae and correlated it to the production of VEGF and MMP-9. The results obtained showed an increased VEGF and MMP-9 production correlated with a time-dependent increase in cellular proliferation in HUVEC infected with C. pneumoniae at a multiplicity of infection (MOI) of 2 IFU/cell. HUVEC preincubated with VEGF antibody did not release MMP-9, as detected by zymography assessment and ELISA assay. In addition, we demonstrated that TLR2/TLR4 are expressed in HUVEC infected with viable microorganisms (25% and 17%, respectively), while UV-inactivated microorganisms induced a lesser expression (20% and 11%, respectively) compared to control cells and HUVEC exposed to heat-killed bacteria showed a percentage of TLR-expressing cells similar to the control cells. In addition, the cells preincubated for 60 min with TLR2/TLR4 neutralizing antibodies showed a decrease in C. pneumonia-induced VEGF and MMP-9 production.

摘要

基质金属蛋白酶(MMP)是一组宿主来源的酶,参与细胞外基质(ECM)分子的周转,特别是 92 kDa 明胶酶 MMP-9 经常被巨噬细胞和平滑肌细胞在动脉粥样硬化斑块中表达。最近的证据支持 Toll 样受体(TLR)信号在动脉粥样硬化病变发展中的作用。在这项研究中,我们分析了感染肺炎衣原体的 HUVEC 中 TLR2/TLR4 的表达,并将其与 VEGF 和 MMP-9 的产生相关联。结果表明,感染肺炎衣原体的 HUVEC 中 VEGF 和 MMP-9 的产生增加与细胞增殖呈时间依赖性增加相关,感染复数(MOI)为 2 IFU/细胞。HUVEC 在用 VEGF 抗体预处理后,通过明胶酶谱分析和 ELISA 检测未释放 MMP-9。此外,我们证明 TLR2/TLR4 在感染活微生物的 HUVEC 中表达(分别为 25%和 17%),而紫外线灭活的微生物诱导的表达水平较低(分别为 20%和 11%),与对照细胞和暴露于热灭活细菌的 HUVEC 相比,TLR 表达细胞的百分比与对照细胞相似。此外,用 TLR2/TLR4 中和抗体预处理 60 分钟的细胞显示肺炎衣原体诱导的 VEGF 和 MMP-9 产生减少。

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