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Novel automated tracking analysis of particles subjected to shear flow: Kindlin-3 role in B cells

机译:新型的剪切流自动跟踪分析:Kindlin-3在B细胞中的作用

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摘要

Shear flow assays are used to mimic the influence of physiological shear force in diverse situations such as leukocyte rolling and arrest on the vasculature, capture of nanoparticles, and bacterial adhesion. Analysis of such assays usually involves manual counting, is labor-intensive, and is subject to bias. We have developed the Leukotrack program that incorporates a novel (to our knowledge) segmentation routine capable of reliable detection of cells in phase contrast images. The program also automatically tracks rolling cells in addition to those that are more firmly attached and migrating in random directions. We demonstrate its use in the analysis of lymphocyte arrest mediated by one or more active conformations of the integrin LFA-1. Activation of LFA-1 is a multistep process that depends on several proteins including kindlin-3, the protein that is mutated in leukocyte adhesion deficiency-III patients. We find that the very first stage of LFA-1-mediated attaching is unable to proceed in the absence of kindlin-3. Our evidence indicates that kindlin-3-mediated high-affinity LFA-1 controls both the early transient integrin-dependent adhesions in addition to the final stable adhesions made under flow conditions.
机译:剪切流测定法用于模拟在各种情况下的生理剪切力的影响,例如白细胞滚动和停滞对脉管系统,纳米颗粒的捕获以及细菌粘附。此类分析的分析通常涉及手动计数,劳动强度大且容易产生偏差。我们已经开发了Leukotrack程序,该程序结合了一种新颖(据我们所知)的分割程序,能够可靠地检测相衬图像中的细胞。该程序还可以自动跟踪滚动单元,以及那些更牢固地附着并在随机方向上迁移的单元。我们证明其用于分析整合素LFA-1的一种或多种活性构象介导的淋巴细胞停滞。 LFA-1的激活是一个多步骤过程,取决于几种蛋白质,包括kindlin-3,该蛋白质在白细胞粘附缺乏症III型患者中发生突变。我们发现,在缺乏kindlin-3的情况下,LFA-1介导的附着的第一阶段无法进行。我们的证据表明,kinelin-3介导的高亲和力LFA-1除了控制在流动条件下产生的最终稳定黏附以外,还控制了早期短暂的整合素依赖性黏附。

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