Dexter C M, Corley R B
Eur J Immunol. 1987 Jun;17(6):867-71. doi: 10.1002/eji.1830170621.
The expression of IgG Fc receptor (FcR) molecules was examined on Ly-1+ B cells and B cells tumors. FcR molecules were found on a representative Ly-1+ B cell lymphoma of the pre-B and as well as of the mature cell B phenotypes. The expression of the FcR did not change on these cells during their differentiation to B cells or to antibody-secreting cells, respectively. Ly-1+ B cells were found at low frequency (approximately 2%) in the spleens of normal mice, and in the peritoneal cavity where their representation was greater. The frequency of Ly-1+ B cells declined after birth, although their numbers increased in both organs. These Ly-1+ B cells expressed the FcR molecule throughout ontogeny. Furthermore, the amount of FcR expressed on Ly-1+ B cells was similar to the levels expressed on their "conventional" (Ly-1-) B cell counterparts. The FcR was also found on Ly-1+ B cells from autoimmune mice. The significance of the expression of FcR molecules on Ly-1+ B cells is discussed.
在Ly-1+B细胞和B细胞肿瘤上检测了IgG Fc受体(FcR)分子的表达。在B前体细胞以及成熟B细胞表型的代表性Ly-1+B细胞淋巴瘤上发现了FcR分子。在这些细胞分别分化为B细胞或抗体分泌细胞的过程中,FcR的表达没有变化。Ly-1+B细胞在正常小鼠脾脏中的频率较低(约2%),而在腹腔中其比例更高。出生后Ly-1+B细胞的频率下降,尽管它们在两个器官中的数量都增加了。这些Ly-1+B细胞在个体发育过程中都表达FcR分子。此外,Ly-1+B细胞上表达的FcR量与它们的“传统”(Ly-1-)B细胞对应物上表达的水平相似。在自身免疫小鼠的Ly-1+B细胞上也发现了FcR。讨论了Ly-1+B细胞上FcR分子表达的意义。