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可溶性选择素和细胞间黏附分子-1在体外调节中性粒细胞与内皮细胞的黏附及穿膜迁移。

Soluble selectins and ICAM-1 modulate neutrophil-endothelial adhesion and diapedesis in vitro.

作者信息

Ohno N, Ichikawa H, Coe L, Kvietys P R, Granger D N, Alexander J S

机构信息

Department of Physiology, LSU Medical Center, Shreveport 71130, USA.

出版信息

Inflammation. 1997 Jun;21(3):313-24. doi: 10.1023/a:1027349900279.

Abstract

We observed that normal plasma dramatically reduces neutrophil-endothelial adhesion. Therefore, we identified factors in plasma which might limit PMN adhesion in vitro. We found that the anti-adhesive effect was not mediated by vasoactive lipids present in plasma. Immunoprecipitation of soluble adhesion molecules, P and E-selectins and ICAM-1 restored PMN adhesion to control values. We further examined whether soluble adhesion molecules in plasma might also regulate PMN endothelial migration in response to fMLP (10(-6) M). Plasma significantly reduced PMN migration, and this effect was prevented only by the simultaneous removal of soluble P and E selectins and ICAM-1 together, but not individually. These data show that soluble selectins and ICAM-1 may regulate PMN adhesion and diapedesis, and that alterations in the levels of these molecules may regulate PMN-endothelial interactions in vivo.

摘要

我们观察到正常血浆可显著降低中性粒细胞与内皮细胞的黏附。因此,我们鉴定了血浆中可能在体外限制PMN黏附的因子。我们发现这种抗黏附作用不是由血浆中存在的血管活性脂质介导的。对可溶性黏附分子、P和E选择素以及细胞间黏附分子-1进行免疫沉淀后,PMN黏附恢复到对照值。我们进一步研究血浆中的可溶性黏附分子是否也可能调节PMN对fMLP(10⁻⁶ M)的内皮迁移。血浆显著降低了PMN迁移,并且只有同时去除可溶性P和E选择素以及细胞间黏附分子-1才能阻止这种作用,单独去除则无效。这些数据表明可溶性选择素和细胞间黏附分子-1可能调节PMN的黏附和渗出,并且这些分子水平的改变可能在体内调节PMN与内皮细胞的相互作用。

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