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用于表型和功能分析的稀有抗原特异性B细胞的检测与富集

Detection and Enrichment of Rare Antigen-specific B Cells for Analysis of Phenotype and Function.

作者信息

Smith Mia J, Packard Thomas A, O'Neill Shannon K, Hinman Rochelle M, Rihanek Marynette, Gottlieb Peter A, Cambier John C

机构信息

Department of Immunology and Microbiology, University of Colorado School of Medicine; Department of Microbiology, Immunology, and Pathology, Colorado State University.

Department of Immunology and Microbiology, University of Colorado School of Medicine.

出版信息

J Vis Exp. 2017 Feb 16(120):55382. doi: 10.3791/55382.

Abstract

B cells reactive with a specific antigen usually occur at a frequency of <0.05% of lymphocytes. For decades researchers have sought methods to isolate and enrich these rare cells for studies of their phenotype and biology. Approaches are inevitably based on the principle that B cells recognize native antigen by virtue of cell surface receptors that are representative in specificity of antibodies that will eventually be secreted by their differentiated daughters. Perhaps the most obvious approach to the problem involves use of fluorochrome-conjugated antigens in conjunction with fluorescence-activated cell sorting (FACS). However, the utility of these methods is limited by cell frequency and the achievable rate of analysis and isolation by electronic sorting. A novel method to enrich rare antigen-specific B cells using magnetic nanoparticles that results in high yield enrichment of antigen-reactive B cells from large starting cell populations is described. This method enables improved monitoring of the phenotype and biology of antigen reactive cells before and following in vivo antigen encounter, such as after immunization or during development of autoimmunity.

摘要

与特定抗原发生反应的B细胞通常占淋巴细胞的比例不到0.05%。几十年来,研究人员一直在寻找分离和富集这些稀有细胞的方法,以研究它们的表型和生物学特性。这些方法不可避免地基于这样一个原理,即B细胞通过细胞表面受体识别天然抗原,这些受体在其分化后代最终分泌的抗体特异性方面具有代表性。解决这个问题最明显的方法可能是将荧光染料偶联抗原与荧光激活细胞分选(FACS)结合使用。然而,这些方法的实用性受到细胞频率以及通过电子分选可实现的分析和分离速率的限制。本文描述了一种使用磁性纳米颗粒富集稀有抗原特异性B细胞的新方法,该方法可从大量起始细胞群体中高产率富集抗原反应性B细胞。这种方法能够更好地监测体内抗原接触前后,如免疫后或自身免疫发展过程中,抗原反应性细胞的表型和生物学特性。

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