T细胞受体
生物
基因重排
淋巴母细胞
基因
B细胞
细胞培养
分子生物学
T细胞
抗原
遗传学
抗体
免疫系统
作者
Mary Ann Robinson,Thomas J. Kindt
出处
期刊:Journal of Immunology
[The American Association of Immunologists]
日期:1988-02-15
卷期号:140 (4): 1327-1334
被引量:5
标识
DOI:10.4049/jimmunol.140.4.1327
摘要
Abstract Transformation of peripheral blood lymphocytes by co-incubation with EBV produces B lymphoblastoid cell lines, but rearrangement of TCR beta-chain genes was observed in three different cell lines derived from two individuals. Because rearrangement of TCR genes in B lymphocytes is considered a rare event, these B lymphoblastoid cell lines with rearranged TCR beta-genes were examined in detail to determine whether there were any additional characteristics to distinguish them from B lymphoblastoid cell lines with germ-line TCR beta-genes. All B lymphoblastoid cell lines contained rearranged Ig H and kappa L chain genes, secreted Ig, and expressed B and not T cell surface markers. Cell lines with rearranged TCR beta-genes had rearranged both IgH genes and had rearranged and subsequently deleted both kappa C region genes. Furthermore all three B lymphoblastoid cell lines with rearranged TCR beta-genes produced small amounts of Ig with lambda-L chains. Although the cellular mechanisms maintaining lineage-specific rearrangement events remain unknown, extensive Ig gene rearrangement and inefficient Ig production by B cells may be indicators of a cellular status where normally stringent lineage-specific control elements fail to function efficiently.
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