Kotloff D B, Cebra J J
Department of Biology, University of Pennsylvania, Philadelphia 19104-6018.
Mol Immunol. 1988 Feb;25(2):147-55. doi: 10.1016/0161-5890(88)90062-4.
Antibody isotype expression by B cell clones was analyzed using in vitro microcultures containing low numbers of hapten-gelatin-enriched B cells and higher numbers of hemocyanin-specific helper T cell lines or clones. Twenty-eight to sixty-three percent of clones grown in microculture with haptenated hemocyanin and T cells from established lines expressed IgG and/or IgA isotypes in random mixtures, almost always accompanied by IgM. Helper T cells from hemocyanin-specific clones also supported the expression of non-IgM isotypes by the B cell clones, suggesting that a single specificity of T cell can provide sufficient growth and differentiation factors for the display of isotype switching. A positive correlation between the antibody output of clones and the expression of non-IgM isotypes indicated that the switching process may be associated with cell division. Although memory B cells that give clones expressing IgG and/or IgA in the absence of IgM are also enriched on haptenated gelatin, they are not stimulable under conditions of this microculture assay.
利用体外微量培养法分析了B细胞克隆的抗体亚型表达情况,该微量培养体系含有少量富含半抗原-明胶的B细胞以及较多数量的血蓝蛋白特异性辅助性T细胞系或克隆。在含有半抗原化血蓝蛋白和来自已建立细胞系的T细胞的微量培养中,28%至63%的克隆表达IgG和/或IgA亚型,呈随机混合,几乎总是伴有IgM。来自血蓝蛋白特异性克隆的辅助性T细胞也支持B细胞克隆表达非IgM亚型,这表明单一特异性的T细胞能够为亚型转换的展示提供足够的生长和分化因子。克隆的抗体产量与非IgM亚型的表达之间呈正相关,这表明转换过程可能与细胞分裂有关。虽然在没有IgM的情况下产生表达IgG和/或IgA克隆的记忆B细胞在半抗原化明胶上也有富集,但在这种微量培养分析条件下它们不可被刺激。