首页> 美国卫生研究院文献>Journal of the Boston Society of Medical Sciences >Targeted Recycling of the Lateral Border Recycling Compartment Precedes Adherens Junction Dissociation during Transendothelial Migration
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Targeted Recycling of the Lateral Border Recycling Compartment Precedes Adherens Junction Dissociation during Transendothelial Migration

机译:在跨内皮迁移过程中侧向边界回收室的目标回收先于粘附结分离。

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摘要

Leukocyte transendothelial migration (TEM) requires two major events: local dissociation of adherens junctions manifested as gaps in vascular endothelial (VE)-cadherin staining at the site of TEM and targeted trafficking of the lateral border recycling compartment (LBRC) to the site of TEM. However, the association between LBRC recycling and VE-cadherin gaps remains unknown. We found that when targeting of the LBRC is selectively inhibited using established methods, such as a function blocking anti–platelet endothelial cell adhesion molecule 1 antibody, depolymerizing microtubules, or microinjection of an antibody that inhibits kinesin, VE-cadherin gaps do not form around the blocked leukocyte. This is the first time that the LBRC has been implicated in this process. We obtained similar results for neutrophils and monocytes and in studies using live cell imaging microscopy conducted under fluid shear conditions. Depolymerizing microtubules did not affect the ability of leukocytes to induce tyrosine phosphorylation of VE-cadherin. A VE-cadherin double mutant (Y658F, Y731F) expressed in endothelial cells acted as a dominant negative and inhibited VE-cadherin gap formation and TEM, yet targeting of the LBRC still occurred. These data suggest that targeting of the LBRC to the site of TEM precedes VE-cadherin clearance. Recruitment of the LBRC may play a role in clearing VE-cadherin from the site of TEM.
机译:白细胞跨内皮迁移(TEM)需要两个主要事件:粘附连接的局部解离,表现为TEM部位的血管内皮(VE)-钙黏着蛋白染色的间隙,以及侧向边界回收室(LBRC)的定向转运到TEM部位。但是,LBRC回收与VE-钙粘蛋白缺口之间的关联仍然未知。我们发现,使用已建立的方法(例如功能阻断抗血小板内皮细胞粘附分子1抗体,解聚微管或显微注射抑制驱动蛋白的抗体)选择性抑制LBRC的靶向作用时,在周围不会形成VE-钙粘蛋白间隙阻塞的白细胞。这是LBRC首次涉入这一过程。对于嗜中性粒细胞和单核细胞,以及在流体剪切条件下使用活细胞成像显微镜进行的研究中,我们获得了相似的结果。解聚微管不影响白细胞诱导VE-钙黏着蛋白酪氨酸磷酸化的能力。在内皮细胞中表达的VE-钙黏着蛋白双突变体(Y658F,Y731F)起显性负性作用,并抑制VE-钙黏着蛋白间隙形成和TEM,但是仍然靶向LBRC。这些数据表明,在VE-钙粘蛋白清除之前,将LBRC靶向TEM部位。 LBRC的招募可能在清除TEM部位的VE-钙黏着蛋白方面发挥了作用。

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