Identification of antigen‐specific B cells by concurrent monitoring of intracellular Ca<sup>2+</sup> mobilization and antigen binding with microwell array chip system equipped with a CCD imager
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<jats:title>Abstract</jats:title><jats:p>B cells are very heterogeneous, consisting of more than 10<jats:sup>9</jats:sup> B‐cell clones with distinct specificities for antigens in each individual. To identify single B cells with antigen specificity, we have been developing cell microarray technology using microwell array chips whose microwells each capture a single B cell. Using microwell array chips, we detected antigen‐specific B cells by monitoring antigen‐induced intracellular Ca<jats:sup>2+</jats:sup> mobilization with a CCD scanner (MAC‐CCD system) or the binding of fluorescence‐labeled antigen to cells with a confocal laser scanner. We retrieved target cells from the chip, cloned immunoglobulin genes, and produced antigen‐specific antibodies. However, these methods present some difficulties: the former technique could not detect cells whose frequency was less than 0.05% and the latter one took a long time to identify the objective cells although it could detect cells at a frequency of 0.01%. Here, we have combined the advantages of these two methods. Monitoring antigen‐induced intracellular Ca<jats:sup>2+</jats:sup> mobilizations and the binding of fluorescence‐labeled antigens simultaneously with a MAC‐CCD system enabled us to detect rapidly, antigen‐specific B cells whose frequency was less than 0.01% with high efficiency. Our system provides a superior screening system for antigen‐specific B cells and extends the horizons of multiparameter single‐cell analysis in heterogeneous cell populations. © 2009 International Society for Advancement of Cytometry</jats:p>
収録刊行物
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- Cytometry Part A
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Cytometry Part A 75A (8), 682-687, 2009-06-12
Wiley