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仿生毛细血管后微静脉扩张用于白细胞黏附研究。

Biomimetic post-capillary venule expansions for leukocyte adhesion studies.

机构信息

Department of Pathology, Case Western Reserve University School of Medicine, Cleveland, OH, 44106, USA.

Case Western Reserve University School of Medicine, Cleveland, OH, 44106, USA.

出版信息

Sci Rep. 2018 Jun 19;8(1):9328. doi: 10.1038/s41598-018-27566-z.

Abstract

Leukocyte adhesion and extravasation are maximal near the transition from capillary to post-capillary venule, and are strongly influenced by a confluence of scale-dependent physical effects. Mimicking the scale of physiological vessels using in vitro microfluidic systems allows the capture of these effects on leukocyte adhesion assays, but imposes practical limits on reproducibility and reliable quantification. Here we present a microfluidic platform that provides multiple (54-512) technical replicates within a 15-minute sample collection time, coupled with an automated computer vision analysis pipeline that captures leukocyte adhesion probabilities as a function of shear and extensional stresses. We report that in post-capillary channels of physiological scale, efficient leukocyte adhesion requires erythrocytes forcing leukocytes against the wall, a phenomenon that is promoted by the transitional flow in post-capillary venule expansions and dependent on the adhesion molecule ICAM-1.

摘要

白细胞黏附和渗出作用在从毛细血管向毛细血管后微静脉过渡的部位最为强烈,并且强烈受到多种尺度相关物理效应的影响。使用体外微流控系统模拟生理血管的尺度可以在白细胞黏附测定中捕获这些效应,但在可重复性和可靠的定量方面存在实际限制。在这里,我们提出了一种微流控平台,该平台在 15 分钟的样本采集时间内提供了多个(54-512)技术重复,并结合了自动化计算机视觉分析管道,可以捕获白细胞黏附的概率作为剪切和拉伸应力的函数。我们报告说,在生理尺度的毛细血管后通道中,有效的白细胞黏附需要红细胞将白细胞推向壁面,这种现象是由毛细血管后微静脉扩张处的过渡流促进的,并且依赖于黏附分子 ICAM-1。

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