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人冠状动脉内皮细胞在胶原蛋白三维培养模型中对W83的反应

Human Coronary Artery Endothelial Cell Response to W83 in a Collagen Three-Dimensional Culture Model.

作者信息

Cardona-Mendoza Andrés, Roa Molina Nelly Stella, Castillo Diana Marcela, Lafaurie Gloria Inés, Gualtero Escobar Diego Fernando

机构信息

Grupo de Inmunología Celular y Molecular Universidad El Bosque-INMUBO, Vicerrectoría de Investigaciones, Facultad de Odontología, Universidad El Bosque, Bogota 11001, Colombia.

Unidad de Investigación Básica Oral-UIBO, Vicerrectoría de Investigaciones, Facultad de Odontología, Universidad El Bosque, Bogota 11001, Colombia.

出版信息

Microorganisms. 2024 Jan 24;12(2):248. doi: 10.3390/microorganisms12020248.

Abstract

has been reported to be an endothelial cell inflammatory response inducer that can lead to endothelial dysfunction processes related to atherosclerosis; however, these studies have been carried out in vitro in cell culture models on two-dimensional (2D) plastic surfaces that do not simulate the natural environment where pathology develops. This work aimed to evaluate the pro-inflammatory response of human coronary artery endothelial cells (HCAECs) to in a 3D cell culture model compared with a 2D cell culture. HCAECs were cultured for 7 days on type I collagen matrices in both cultures and were stimulated at an MOI of 1 or 100 with live W83 for 24 h. The expression of the genes COX-2, eNOS, and vWF and the levels of the pro-inflammatory cytokines thromboxane A2 (TXA-2) and prostaglandin I2 (PGI2) were evaluated. W83 in the 2D cell culture increased IL-8 levels at MOI 100 and decreased MCP-1 levels at both MOI 100 and MOI 1. In contrast, the 3D cell culture induced an increased gene expression of COX-2 at both MOIs and reduced MCP-1 levels at MOI 100, whereas the gene expression of eNOS, vWF, and IL-8 and the levels of TXA2 and PGI2 showed no significant changes. These data suggest that in the collagen 3D culture model, W83 induces a weak endothelial inflammatory response.

摘要

据报道,它是一种内皮细胞炎症反应诱导剂,可导致与动脉粥样硬化相关的内皮功能障碍过程;然而,这些研究是在二维(2D)塑料表面的细胞培养模型中体外进行的,该模型并未模拟病理发生的自然环境。这项工作旨在评估与二维细胞培养相比,人冠状动脉内皮细胞(HCAECs)在三维细胞培养模型中对[具体物质未给出]的促炎反应。在两种培养中,HCAECs均在I型胶原基质上培养7天,并用活的W83以1或100的感染复数刺激24小时。评估了COX-2、eNOS和vWF基因的表达以及促炎细胞因子血栓素A2(TXA-2)和前列腺素I2(PGI2)的水平。二维细胞培养中的W83在感染复数为100时增加了IL-8水平,在感染复数为100和1时均降低了MCP-1水平。相比之下,三维细胞培养在两种感染复数下均诱导COX-2基因表达增加,在感染复数为100时降低MCP-1水平,而eNOS、vWF和IL-8的基因表达以及TXA2和PGI2的水平没有显著变化。这些数据表明,在胶原三维培养模型中,W83诱导了较弱的内皮炎症反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1bb/10892777/389b205fe501/microorganisms-12-00248-g001.jpg

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