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白细胞介素-4和肿瘤坏死因子-α对培养内皮细胞中血管细胞黏附分子-1表达的调控

Regulation of vascular cell adhesion molecule-1 expression by IL-4 and TNF-alpha in cultured endothelial cells.

作者信息

Iademarco M F, Barks J L, Dean D C

机构信息

Department of Medicine, Washington University School of Medicine, St. Louis, Missouri 63110.

出版信息

J Clin Invest. 1995 Jan;95(1):264-71. doi: 10.1172/JCI117650.

Abstract

Interaction between vascular cell adhesion molecule-1 (VCAM-1) on endothelial cells and alpha 4 integrins on leukocytes is thought to mediate the selective recruitment of eosinophils and lymphocytes that occurs in allergic diseases. IL-4 is associated with allergic conditions, and it has been shown to selectively increase expression of VCAM-1 on endothelial cells in vivo, suggesting that it could be responsible for VCAM-1 expression in allergic disease. Using a combination of immunofluorescence, flow cytometry, and Northern analysis, we compared the effect of TNF-alpha and IL-4 on VCAM-1 expression. TNF-alpha is also associated with allergic diseases, and it rapidly increases transcription of the VCAM-1 gene. The effect of IL-4 was relatively modest with prolonged kinetics: VCAM-1 was not detected until 72 h after treatment with IL-4. However, when TNF-alpha and IL-4 were combined, there was a synergistic increase in VCAM-1 expression and a dramatic prolongation of the appearance of VCAM-1 on the cell surface. This synergy results from a combination of transcriptional activation by TNF-alpha and the stabilization of resulting transcripts by IL-4. We propose that IL-4 allows subthreshold concentrations of TNF-alpha (concentrations that would not normally activate expression of adhesion molecules on the endothelium) to selectively increase VCAM-1 expression and to prolong its appearance on the surface of cells in allergic disease.

摘要

内皮细胞上的血管细胞黏附分子-1(VCAM-1)与白细胞上的α4整合素之间的相互作用被认为介导了过敏性疾病中发生的嗜酸性粒细胞和淋巴细胞的选择性募集。白细胞介素-4(IL-4)与过敏状态相关,并且已证明它在体内可选择性增加内皮细胞上VCAM-1的表达,这表明它可能是过敏性疾病中VCAM-1表达的原因。我们使用免疫荧光、流式细胞术和Northern分析相结合的方法,比较了肿瘤坏死因子-α(TNF-α)和IL-4对VCAM-1表达的影响。TNF-α也与过敏性疾病相关,并且它能迅速增加VCAM-1基因的转录。IL-4的作用相对较小且动力学过程较长:在用IL-4处理72小时后才检测到VCAM-1。然而,当TNF-α和IL-4联合使用时,VCAM-1的表达有协同增加,并且在细胞表面出现VCAM-1的时间显著延长。这种协同作用是由TNF-α的转录激活和IL-4对产生的转录本的稳定作用共同导致的。我们提出,IL-4使低于阈值浓度的TNF-α(通常不会激活内皮细胞上黏附分子表达的浓度)能够选择性增加VCAM-1的表达,并延长其在过敏性疾病细胞表面出现的时间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd90/295423/7db97142765b/jcinvest00023-0284-a.jpg

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