Ivanyi J, Hudson L
Immunology. 1978 Dec;35(6):941-5.
The membrane expression of M1 (IgM) and G1 (IgG) allotype markers on peripheral blood lymphocytes was examined by immunofluorescence. In homozygous chickens 15% lymphocytes stained with either anti-M1 or with polyspecific rabbit anti-Ig serum, suggesting that M1 is expressed on the surface of probably all B lymphocytes. In heterozygous M1a/M1b individuals antisera against either allelic antigens reacted with 50% of the total surface Ig positive cells as evidence for the allelic exclusion of surface M1 expression. Donor allotype synthesis was determined from serum allotype levels in congenic cyclophosphamide-treated recipients of lymphoid cells. Treatment of cells with anti-M1 serum prior to transfer inhibited both M1 and G1 allotype synthesis. The treatment of heterozygous (M1a/M1b, G1a/G1e) cells with anti-M1b serum inhibited specifically the synthesis of M1b and G1e allotypes controlled by linked genes from the same parental chromosome. Thus, B cells which had been the targets for anti-M1 antibody mediated suppression are also subject to allelic exclusion.
通过免疫荧光法检测外周血淋巴细胞上M1(IgM)和G1(IgG)同种异型标记物的膜表达。在纯合子鸡中,15%的淋巴细胞用抗M1或多特异性兔抗Ig血清染色,这表明M1可能在所有B淋巴细胞表面表达。在杂合子M1a/M1b个体中,针对任一等位基因抗原的抗血清与50%的总表面Ig阳性细胞发生反应,作为表面M1表达等位基因排斥的证据。从经环磷酰胺处理的同基因淋巴细胞受体血清同种异型水平确定供体同种异型合成。在转移前用抗M1血清处理细胞可抑制M1和G1同种异型合成。用抗M1b血清处理杂合子(M1a/M1b,G1a/G1e)细胞可特异性抑制由来自同一亲本染色体的连锁基因控制的M1b和G1e同种异型的合成。因此,作为抗M1抗体介导抑制靶点的B细胞也存在等位基因排斥。