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组胺可诱导人内皮细胞产生白细胞介素-6。

Histamine induces IL-6 production by human endothelial cells.

作者信息

Delneste Y, Lassalle P, Jeannin P, Joseph M, Tonnel A B, Gosset P

机构信息

Institut Pasteur de Lille, Unité INSERM 416, France.

出版信息

Clin Exp Immunol. 1994 Nov;98(2):344-9. doi: 10.1111/j.1365-2249.1994.tb06148.x.

Abstract

Histamine is one of the major mediators implicated in the physiopathology of allergy. On vascular endothelium, histamine mainly induces early effects: an increase in vasopermeability leading to oedema, a release of lipid mediators and a transient expression of P-selectin. The aim of this study was to evaluate the effects of histamine on adhesion molecule expression and IL-6 production by human endothelial cells. Histamine did not modulate the expression of intercellular adhesion molecule-1 (ICAM-1), vascular cell adhesion molecule-1 (VCAM-1) and E-selectin, but induced a transient expression of P-selectin as previously reported. In addition, histamine increased in a dose- (from 10(-5) to 10(-3) M) and time- (from 4 h to 24 h) dependent fashion the IL-6 synthesis by endothelial cells. Tumour necrosis factor-alpha (TNF-alpha)-induced IL-6 production was also potentiated in a dose-dependent manner by histamine, without modification of the time course of IL-6 secretion. Moreover, this increase of IL-6 production induced by histamine was inhibited in a dose-dependent manner by H1 and H2 histamine receptor antagonists (50% inhibition of IL-6 production at 5 x 10(-4) M and 4 x 10(-5) M, respectively). So, histamine induces, besides already well known effects, a late stimulation of endothelial cells, i.e. the production of IL-6.

摘要

组胺是参与过敏生理病理学的主要介质之一。在血管内皮上,组胺主要诱导早期效应:血管通透性增加导致水肿、脂质介质释放以及P-选择素的瞬时表达。本研究的目的是评估组胺对人内皮细胞黏附分子表达和白细胞介素-6(IL-6)产生的影响。组胺未调节细胞间黏附分子-1(ICAM-1)、血管细胞黏附分子-1(VCAM-1)和E-选择素的表达,但如先前报道的那样诱导了P-选择素的瞬时表达。此外,组胺以剂量(从10⁻⁵到10⁻³ M)和时间(从4小时到24小时)依赖性方式增加内皮细胞的IL-6合成。组胺还以剂量依赖性方式增强肿瘤坏死因子-α(TNF-α)诱导的IL-6产生,而不改变IL-6分泌的时间进程。此外,组胺诱导的IL-6产生增加被组胺H1和H2受体拮抗剂以剂量依赖性方式抑制(分别在5×10⁻⁴ M和4×10⁻⁵ M时抑制IL-6产生的50%)。因此,组胺除了诱导已知的效应外,还诱导内皮细胞的晚期刺激,即IL-6的产生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ad/1534408/f4c0fe40705c/clinexpimmunol00016-0177-a.jpg

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