Kearney J F, Cooper M D, Lawton A R
J Immunol. 1976 Nov;117(5 Pt 1):1567-72.
Direct immunofluorescence was used to determine the classes of immunoglobulins expressed on the surface membrane and in the cytoplasm of newborn and adult B lymphocytes differentiating in response to LPS in vitro. In both newborn and adult spleen, a small proportion of IgM-bearing B lymphocytes also stained for IgG2; adult spleen contained an additional population of lymphocytes bearing IgG2 alone. Combined surface and cytoplasmic staining at intervals after culture initiation and demonstrated both IgM and IgG2 on the membranes of the earliest cells synthesizing cytoplasmic IgG2. At later stages the proportion of IgM-IgG2 surface doubles and of cells synthesizing cytoplasmic IgG2 which had surface IgM fell significantly. Detection of surface IgM on IgG2 precursors correlated with susceptibility of the IgG2 precursors to anti-mu-suppression over the first 3 days in cultures of newborn spleen cells. After 3 days when these cells no longer expressed surface IgM, 2gG2 responses were not suppressed although the IgM response was still inhibited. These results suggest that virgin IgG2 precursors may be B lymphocytes expressing both IgM and IgG2, and that "switching" involves the loss of IgM receptors as these cells proliferate and mature.
采用直接免疫荧光法来确定体外对脂多糖(LPS)作出反应而分化的新生和成年B淋巴细胞的表面膜和细胞质中所表达的免疫球蛋白类别。在新生和成年脾脏中,一小部分带有IgM的B淋巴细胞也被IgG2染色;成年脾脏中还存在另外一群仅带有IgG2的淋巴细胞。在培养开始后的不同时间进行表面和细胞质联合染色,结果显示最早合成细胞质IgG2的细胞的膜上同时存在IgM和IgG2。在后期,表面IgM-IgG2双阳性细胞以及合成细胞质IgG2且表面有IgM的细胞比例显著下降。在新生脾细胞培养的头3天里,IgG2前体细胞表面IgM的检测结果与这些前体细胞对抗μ抑制的敏感性相关。3天后,当这些细胞不再表达表面IgM时,IgG2反应不再受到抑制,尽管IgM反应仍被抑制。这些结果表明,未成熟的IgG2前体细胞可能是同时表达IgM和IgG2的B淋巴细胞,并且随着这些细胞的增殖和成熟,“类别转换”涉及IgM受体的丢失。