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通过与中性粒细胞相互作用,内皮细胞释放人单核细胞趋化因子。

Release of chemoattractants for human monocytes from endothelial cells by interaction with neutrophils.

作者信息

Schratzberger P, Dunzendorfer S, Reinisch N, Kähler C M, Herold M, Wiedermann C J

机构信息

Department of Internal Medicine, Medical Faculty, University of Innsbruck, Austria.

出版信息

Cardiovasc Res. 1998 May;38(2):516-21. doi: 10.1016/s0008-6363(98)00014-5.

Abstract

OBJECTIVE

The release of monocyte chemoattractant protein-1 (MCP-1) in the vessel wall may lead to accumulation of monocytes in the subendothelial space. The role of neutrophils (PMNL) in the initiation of this process is unknown. We tested whether PMNL are able to induce the production and release of MCP-1 in endothelial cells.

METHODS

PMNL were allowed to interact with human umbilical vein endothelial cell (HUVEC) monolayers in culture. Culture media were collected and assessed for chemotactic activity on mononuclear leukocytes (MNC) or purified monocytes in a modified Boyden chamber assay. Additionally, MCP-1 levels in supernatants were quantified by ELISA.

RESULTS

Media from unstimulated HUVEC culture supernatants induced a slight increase (1.2-fold) of MNC and purified monocyte chemotaxis, which was significantly augmented by addition of PMNL for 1 h (1.4-fold; P < 0.05). The increase in chemotaxis was time- and dose-dependent and could be blocked by an anti-MCP-1 monoclonal antibody. Media obtained after coculture of PMNL and HUVEC for 1-5 h contained increased amounts of MCP-1 as measured by ELISA; addition of cycloheximide abolished this response.

CONCLUSIONS

Interaction of PMNL with endothelium induces the release of functionally active MCP-1 suggesting that in the vascular wall, PMNL may play a role in the recruitment of MNC.

摘要

目的

血管壁中单核细胞趋化蛋白-1(MCP-1)的释放可能导致单核细胞在内皮下间隙积聚。中性粒细胞(PMNL)在这一过程起始阶段的作用尚不清楚。我们测试了PMNL是否能够诱导内皮细胞产生和释放MCP-1。

方法

使PMNL与培养中的人脐静脉内皮细胞(HUVEC)单层相互作用。收集培养基,并在改良的Boyden小室试验中评估其对单核白细胞(MNC)或纯化单核细胞的趋化活性。此外,通过酶联免疫吸附测定(ELISA)对上清液中的MCP-1水平进行定量。

结果

未刺激的HUVEC培养上清液诱导MNC和纯化单核细胞趋化性略有增加(1.2倍),加入PMNL 1小时后趋化性显著增强(1.4倍;P<0.05)。趋化性的增加具有时间和剂量依赖性,并且可以被抗MCP-1单克隆抗体阻断。通过ELISA测定,PMNL和HUVEC共培养1至5小时后获得的培养基中MCP-1含量增加;加入放线菌酮消除了这种反应。

结论

PMNL与内皮的相互作用诱导了功能活性MCP-1的释放,这表明在血管壁中,PMNL可能在MNC的募集过程中发挥作用。

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