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混合白细胞反应、氢化可的松及环孢素对内皮细胞和系膜细胞白细胞黏附分子表达的影响

Effects of mixed leukocyte reaction, hydrocortisone and cyclosporine on expression of leukocyte adhesion molecules by endothelial and mesangial cells.

作者信息

Ihm C G, Hong S P, Park J K, Lee T W, Cho B S, Yang M H, Kim M J

机构信息

Department of Internal Medicine, College of Medicine, Kyung Hee University, Seoul, Korea.

出版信息

J Korean Med Sci. 1996 Dec;11(6):495-500. doi: 10.3346/jkms.1996.11.6.495.

DOI:10.3346/jkms.1996.11.6.495
PMID:9008098
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3054252/
Abstract

We investigated the effects of mixed leukocyte reaction (MLR), hydrocortisone (HC) and cyclosporine A (CsA) on the expression of leukocyte adhesion molecules on the mesangial (MC) and endothelial cells (EnC). Cell surface enzyme immunoassay showed that INFnu, IL-1beta, or TNF alpha stimulated expression of ICAM-1, or VCAM-1 on MC after 24 hours. Flow cytometric analysis demonstrated that MLR supernatant induced a marked increase in mean fluorescence of or % of cells highly expressing intercellular adhesion molecule(ICAM)-1 or vascular cell adhesion molecule (VCAM)-1 on both cells after 24 hours (p<0.001). HC treatment(300 ng/ml) during MLR effectively inhibited MLR-induced upregulation of ICAM-1 and VCAM-1 on both cells (p<0.005). When MLR supernatant with HC was added to adhesion molecule assay, there was no inhibitory effect of HC on VCAM-1. CsA treatment (500 ng/ml) during MLR caused a modest decrease in upregulation of VCAM-1 on EnC (p<0.05), but had no effects on ICAM-1 on both cells. CsA directly decreased expression of VCAM-1 on MC. In conclusion, alloreactive lymphocytes and monocytes upregulate the expression of VCAM-1 and ICAM-1 on target cells probably by the mediation of cytokines. HC effectively prevents MLR-induced upregulation of VCAM-1 and ICAM-1. CsA does not increase the expression of VCAM-1 and ICAM-1.

摘要

我们研究了混合淋巴细胞反应(MLR)、氢化可的松(HC)和环孢素A(CsA)对系膜细胞(MC)和内皮细胞(EnC)上白细胞粘附分子表达的影响。细胞表面酶免疫测定显示,24小时后,INFnu、IL-1β或TNFα刺激MC上ICAM-1或VCAM-1的表达。流式细胞术分析表明,24小时后,MLR上清液可诱导两种细胞上高表达细胞间粘附分子(ICAM)-1或血管细胞粘附分子(VCAM)-1的细胞平均荧光或细胞百分比显著增加(p<0.001)。MLR期间HC处理(300 ng/ml)可有效抑制MLR诱导的两种细胞上ICAM-1和VCAM-1的上调(p<0.005)。当将含有HC的MLR上清液添加到粘附分子测定中时,HC对VCAM-1没有抑制作用。MLR期间CsA处理(500 ng/ml)可使EnC上VCAM-1的上调适度降低(p<0.05),但对两种细胞上的ICAM-1没有影响。CsA可直接降低MC上VCAM-1的表达。总之,同种异体反应性淋巴细胞和单核细胞可能通过细胞因子的介导上调靶细胞上VCAM-1和ICAM-1的表达。HC可有效预防MLR诱导的VCAM-1和ICAM-1上调。CsA不会增加VCAM-1和ICAM-1的表达。

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