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用于体外人中性粒细胞趋化和分子分析的生物粒子微阵列

Bioparticle Microarrays for Chemotactic and Molecular Analysis of Human Neutrophil Swarming in vitro.

作者信息

Walters Nicole, Reátegui Eduardo

机构信息

William G. Lowrie Department of Chemical and Biomolecular Engineering, The Ohio State University.

William G. Lowrie Department of Chemical and Biomolecular Engineering, The Ohio State University; Comprehensive Cancer Center, The Ohio State University;

出版信息

J Vis Exp. 2020 Feb 16(156). doi: 10.3791/60544.

Abstract

Neutrophil swarming is a cooperative process by which neutrophils seal off a site of infection and promote tissue reorganization. Swarming has classically been studied in vivo in animal models showing characteristic patterns of cell migration. However, in vivo models have several limitations, including intercellular mediators that are difficult to access and analyze, as well as the inability to directly analyze human neutrophils. Because of these limitations, there is a need for an in vitro platform that studies swarming with human neutrophils and provides easy access to the molecular signals generated during swarming. Here, a multistep microstamping process is used to generate a bioparticle microarray that stimulates swarming by mimicking an in vivo infection. The bioparticle microarray induces neutrophils to swarm in a controlled and stable manner. On the microarray, neutrophils increase in speed and form stable swarms around bioparticle clusters. Additionally, supernatant generated by the neutrophils was analyzed and 16 proteins were discovered to have been differentially expressed over the course of swarming. This in vitro swarming platform facilitates direct analysis of neutrophil migration and protein release in a reproducible, spatially controlled manner.

摘要

中性粒细胞聚集是一个协作过程,通过该过程中性粒细胞封锁感染部位并促进组织重塑。传统上,聚集现象是在动物模型的体内进行研究的,这些研究展示了细胞迁移的特征模式。然而,体内模型存在若干局限性,包括难以获取和分析细胞间介质,以及无法直接分析人类中性粒细胞。由于这些局限性,需要一个体外平台来研究人类中性粒细胞的聚集,并便于获取聚集过程中产生的分子信号。在此,采用多步微冲压工艺生成生物颗粒微阵列,通过模拟体内感染来刺激聚集。该生物颗粒微阵列能以可控且稳定的方式诱导中性粒细胞聚集。在微阵列上,中性粒细胞速度加快,并在生物颗粒簇周围形成稳定的聚集体。此外,对中性粒细胞产生的上清液进行了分析,发现有16种蛋白质在聚集过程中表达存在差异。这个体外聚集平台有助于以可重复、空间可控的方式直接分析中性粒细胞的迁移和蛋白质释放。

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