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在紊乱血流中与平滑肌细胞共培养时,中性粒细胞、淋巴细胞和单核细胞在内皮迁移和内皮下迁移中表现出不同行为。

Neutrophils, lymphocytes, and monocytes exhibit diverse behaviors in transendothelial and subendothelial migrations under coculture with smooth muscle cells in disturbed flow.

作者信息

Chen Cheng-Nan, Chang Shun-Fu, Lee Pei-Ling, Chang Kyle, Chen Li-Jing, Usami Shunichi, Chien Shu, Chiu Jeng-Jiann

机构信息

Institute of Life Sciences, National Defense Medical Center, National Health Research Institutes, Taiwan, Republic of China.

出版信息

Blood. 2006 Mar 1;107(5):1933-42. doi: 10.1182/blood-2005-08-3137. Epub 2005 Nov 17.

DOI:10.1182/blood-2005-08-3137
PMID:16293605
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1895706/
Abstract

Atherosclerosis develops at regions of the arterial tree exposed to disturbed flow. The early stage of atherogenesis involves the adhesion of leukocytes (white blood cells [WBCs]) to and their transmigration across endothelial cells (ECs), which are located in close proximity to smooth muscle cells (SMCs). We investigated the effects of EC/SMC coculture and disturbed flow on the adhesion and transmigration of 3 types of WBCs (neutrophils, peripheral blood lymphocytes [PBLs], and monocytes) using our vertical-step flow (VSF) chamber, in which ECs were cocultured with SMCs in collagen gels. Such coculture significantly increased the adhesion and transmigration of neutrophils, PBLs, and monocytes under VSF, particularly in the reattachment area, where the rolling velocity of WBCs and their transmigration time were decreased, as compared with the other areas. Neutrophils, PBLs, and monocytes showed different subendothelial migration patterns under VSF. Their movements were more random and shorter in distance in the reattachment area. Coculture of ECs and SMCs induced their expressions of adhesion molecules and chemokines, which contributed to the increased WBC adhesion and transmigration. Our findings provide insights into the mechanisms of WBC interaction with the vessel wall (composed of ECs and SMCs) under the complex flow environments found in regions of prevalence for atherogenesis.

摘要

动脉粥样硬化在动脉树中血流紊乱的区域发展。动脉粥样硬化形成的早期阶段涉及白细胞(白血细胞[WBCs])与位于平滑肌细胞(SMCs)附近的内皮细胞(ECs)的黏附及其跨内皮细胞的迁移。我们使用我们的垂直阶梯流(VSF)室研究了EC/SMC共培养和紊乱血流对3种类型白细胞(中性粒细胞、外周血淋巴细胞[PBLs]和单核细胞)黏附和迁移的影响,在该室中,ECs与SMCs在胶原蛋白凝胶中共培养。这种共培养显著增加了VSF条件下中性粒细胞、PBLs和单核细胞的黏附和迁移,特别是在再附着区域,与其他区域相比,白细胞的滚动速度及其迁移时间在此区域降低。中性粒细胞、PBLs和单核细胞在VSF条件下表现出不同的内皮下迁移模式。它们在再附着区域的运动更随机且距离更短。ECs和SMCs的共培养诱导了它们黏附分子和趋化因子的表达,这导致了白细胞黏附和迁移的增加。我们的研究结果为在动脉粥样硬化高发区域发现的复杂血流环境下白细胞与血管壁(由ECs和SMCs组成)相互作用的机制提供了见解。

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The CXCR3 targeting chemokine CXCL11 has potent antitumor activity in vivo involving attraction of CD8+ T lymphocytes but not inhibition of angiogenesis.靶向CXCR3的趋化因子CXCL11在体内具有强大的抗肿瘤活性,涉及吸引CD8 + T淋巴细胞,但不抑制血管生成。
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Coexisting proinflammatory and antioxidative endothelial transcription profiles in a disturbed flow region of the adult porcine aorta.成年猪主动脉紊乱血流区域中共存的促炎和抗氧化内皮转录谱。
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Neointimal smooth muscle cells display a proinflammatory phenotype resulting in increased leukocyte recruitment mediated by P-selectin and chemokines.新生内膜平滑肌细胞表现出促炎表型,导致由P-选择素和趋化因子介导的白细胞募集增加。
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Shear stress increases ICAM-1 and decreases VCAM-1 and E-selectin expressions induced by tumor necrosis factor-[alpha] in endothelial cells.剪切应力增加内皮细胞中由肿瘤坏死因子-α诱导的细胞间黏附分子-1(ICAM-1)表达,并降低血管细胞黏附分子-1(VCAM-1)和E-选择素的表达。
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