生物
生发中心
慢性淋巴细胞白血病
分子生物学
B-1电池
人口
幼稚B细胞
B细胞
多克隆B细胞反应
骨髓
受体
B细胞受体
免疫系统
白血病
医学
细胞生物学
免疫学
T细胞
抗体
抗原提呈细胞
遗传学
环境卫生
作者
Andrew G. Polson,Bing Zheng,Kristi Elkins,Wesley Chang,Changchun Du,Patrick F. Dowd,Lulu Yen,Christine Tan,Jo-Anne Hongo,Hartmut Koeppen,Allen Ebens
标识
DOI:10.1093/intimm/dxl069
摘要
A new family of Ig domain receptors referred to as the immune receptor translocation-associated (IRTA) proteins, FcR homologs (FcRHs) or FcR-like that are expressed in lymphoid cells has been recently described. RNA expression analysis suggests that FcRH1-5/IRTA1-5 are expressed exclusively in subsets of the B-cell compartment. We generated mAbs to FcRH1-5/IRTA1-5 and examined their protein expression pattern in normal tissue and in chronic lymphocytic leukemia (CLL) cells. Our data indicated that FcRH1-5/IRTA1-5 were expressed in B-cell sub-populations; however, in some cases, the protein was not expressed in the same B-cell populations as suggested by the RNA expression analysis. FcRH1/IRTA5 was expressed throughout the B-cell lineage starting at the pro-B-cell stage but was down-regulated in plasma cells. FcRH2/IRTA4 was expressed preferentially in memory B cells. FcRH3/IRTA3 was expressed at low levels in naive, germinal center (GC) and memory B cells but was also expressed in NK cells. FcRH4/IRTA1 was expressed in a sub-population of memory B cells associated with mucosal tissue. FcRH5/IRTA2 was expressed in mature B cells and memory B cells and down-regulated in GC cells and, unlike all other B-cell-specific markers, maintained its expression in plasma cells from tonsil, spleen and bone marrow. We examined the expression of FcRH1-5/IRTA1-5 on the surface of CLL cells and found a similar pattern of expression on CLL cells as in the normal mature B cells, except for FcRH3/IRTA3 which was up-regulated in CLL.
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