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降钙素基因相关肽抑制人真皮微血管内皮细胞趋化因子的产生。

Calcitonin gene-related peptide inhibits chemokine production by human dermal microvascular endothelial cells.

机构信息

Department of Dermatology, Weill Cornell Medical College, New York, NY 10021, USA.

出版信息

Brain Behav Immun. 2011 May;25(4):787-99. doi: 10.1016/j.bbi.2011.02.007. Epub 2011 Feb 18.

DOI:10.1016/j.bbi.2011.02.007
PMID:21334428
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3081395/
Abstract

This study examined whether the sensory neuropeptide calcitonin gene-related peptide (CGRP) inhibits release of chemokines by dermal microvascular endothelial cells. Dermal blood vessels are associated with nerves containing CGRP, suggesting that CGRP-containing nerves may regulate cutaneous inflammation through effects on vessels. We examined CGRP effects on stimulated chemokine production by a human dermal microvascular endothelial cell line (HMEC-1) and primary human dermal microvascular endothelial cells (pHDMECs). HMEC-1 cells and pHDMECs expressed mRNA for components of the CGRP and adrenomedullin receptors and CGRP inhibited LPS-induced production of the chemokines CXCL8, CCL2, and CXCL1 by both HMEC-1 cells and pHDMECs. The receptor activity-modifying protein (RAMP)1/calcitonin receptor-like receptor (CL)-specific antagonists CGRP₈-₃₇ and BIBN4096BS, blocked this effect of CGRP in a dose-dependent manner. CGRP prevented LPS-induced IκBα degradation and NF-κB binding to the promoters of CXCL1, CXCL8 and CCL2 in HMEC-1 cells and Bay 11-7085, an inhibitor of NF-κB activation, suppressed LPS-induced production of CXCL1, CXCL8 and CCL2. Thus, the NF-κB pathway appears to be involved in CGRP-mediated suppression of chemokine production. Accordingly, CGRP treatment of LPS-stimulated HMEC-1 cells inhibited their ability to chemoattract human neutrophils and mononuclear cells. Elucidation of this pathway may suggest new avenues for therapeutic manipulation of cutaneous inflammation.

摘要

这项研究旨在探讨感觉神经肽降钙素基因相关肽 (CGRP) 是否抑制真皮微血管内皮细胞释放趋化因子。皮肤血管与含有 CGRP 的神经有关,这表明含有 CGRP 的神经可能通过对血管的影响来调节皮肤炎症。我们研究了 CGRP 对人真皮微血管内皮细胞系 (HMEC-1) 和原代人真皮微血管内皮细胞 (pHDMEC) 刺激产生趋化因子的影响。HMEC-1 细胞和 pHDMEC 表达 CGRP 和肾上腺髓质素受体的成分的 mRNA,CGRP 抑制 LPS 诱导的 HMEC-1 细胞和 pHDMEC 产生趋化因子 CXCL8、CCL2 和 CXCL1。受体活性修饰蛋白 (RAMP)1/降钙素受体样受体 (CL) 特异性拮抗剂 CGRP₈-₃₇ 和 BIBN4096BS 以剂量依赖性方式阻断 CGRP 的这种作用。CGRP 可防止 LPS 诱导的 HMEC-1 细胞中 IκBα 降解和 NF-κB 与 CXCL1、CXCL8 和 CCL2 启动子的结合,NF-κB 激活抑制剂 Bay 11-7085 抑制 LPS 诱导的 CXCL1、CXCL8 和 CCL2 的产生。因此,NF-κB 途径似乎参与了 CGRP 介导的趋化因子产生抑制。因此,CGRP 处理 LPS 刺激的 HMEC-1 细胞抑制了它们趋化人类中性粒细胞和单核细胞的能力。阐明该途径可能为治疗性操纵皮肤炎症提供新的途径。

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