[CD11/CD18对早期烧伤后内皮细胞与PMN粘附及其表达的影响]。

Z Li, Z Yang, X Luo
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引用次数: 0

摘要

本研究旨在探讨烧伤患者烧伤后早期多形核中性粒细胞(PMN)中CD11a/CD18和CD11b/CD18的表达及CD11/CD18单抗对PMN-EC粘附和PMN诱导的内皮细胞(EC)损伤的影响。烧伤患者PMN与人脐静脉内皮细胞(HUVEC)孵育24 h后,测定PMN与EC的粘附率、过滤系数(kf)和单层体积通量(Jv)。采用CD11a/CD18单克隆抗体(mAb)和CD11b/CD18单克隆抗体预处理烧伤患者pmn,以验证CD11/CD18在PMN-EC粘附和EC损伤中的作用。烧伤后1、3、5、7 d采用流式细胞术检测CD11a/CD18和CD11b/CD18的表达。结果表明,烧伤患者PMNs上CD11a/CD18和CD11b/CD18的表达迅速增加,在烧伤后第1天达到峰值,并在烧伤后第7天保持较高水平。在微孔过滤膜上培养的HUVECs与烧伤患者PMNs孵育后,Kf和Jv值明显升高。用CD11a/CD18单抗和CD11b/CD18单抗预处理烧伤患者PMNs后,PMN-HUVEC黏附率被抑制70% ~ 80%,Jv和kf值明显降低。提示烧伤后PMNs上CD11a/CD18和CD11b/CD18表达增加。烧伤患者PMNs可损伤EC,增加EC单层通透性(kf, Jv)。CD11/CD18单抗抑制PMN-EC粘附,减轻pmn诱导的EC损伤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Effects of CD11/CD18 on adhesion between endothelial cell and PMN and its expression in early stage postburn].

This study was to investigate the expressions of CD11a/CD18 and CD11b/CD18 on burn patient's polymorphonuclear neutrophil (PMN) in early postburn stage and effects of CD11/CD18 mAb on PMN-EC adhesion and endothelial cell (EC) damage induced by PMN. Adhesive rate between PMN and EC, the filtration coefficient (kf) and monolayer volume flux (Jv) were determined after incubating burn patient's PMN with human umbilical vein endothelial cell (HUVEC) for 24 hours. CD11a/CD18 monoclonal antibodies (mAb) and CD11b/CD18 mAb were used to pretreat burn patient's PMNs in order to demonstrate the role of CD11/CD18 in PMN-EC adhesion and EC damage. Expressions of CD11a/CD18 and CD11b/CD18 were determined by flow cytometry 1, 3, 5, 7 d postburn. The results indicated that expressions of CD11a/CD18 and CD11b/CD18 on burn patient's PMNs increased quickly, reaching the peak on day 1 postburn and remained in high level till 7 days postburn. The values of Kf and Jv were increased markedly after burn patient's PMNs was incubated with HUVECs, which were cultured on micropore filter membrane. When burn patient's PMNs were pretreated with CD11a/CD18 mAb and CD11b/CD18 mAb, PMN-HUVEC adhesive rate was inhibited by 70%-80% and the values of Jv and kf were decreased significantly. It suggested that there were increased expressions of CD11a/CD18 and CD11b/CD18 on PMNs after burn injury. Burn patient's PMNs could damage EC and increased EC monolayer permeability (kf, Jv). CD11/CD18 mAb inhibited PMN-EC adhesion and attenuated EC damage induced by PMNs.

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