Freund J G, Ahmed A, Budd R E, Dorf M E, Sell K W, Vannier W E, Humphreys R E
J Immunol. 1976 Nov;117(5 Pt.2):1903-5.
The L1210 murine lymphoblast cell line possessed a B lymphocyte-specific alloantigen which was detected with C57BL/Ks anti-L1210 serum. The antigen was found on splenic B lymphocytes but not on thymocytes, T lymphocytes, or erythrocytes. It was present on only 7% of bone marrow cells. The reactivity of C57BL/Ks anti-DBA/2-spleen serum was indistinguishable from that of the anti L1210 serum, confirming that the antigen was a normal component of B lymphocytes of the CBA/2 mouse. The strain distribution pattern of the antigen detected by the C57BL/Ks anti-L1210 serum indicated that this alloantigen was not an allele of the H-2K, H-2D, Mls, or Ig loci. Genetic analysis indicated that the antigen was inherited as a single, Mendelian dominant trait. Segregation analysis of (B10.BR X DBA/2)F1 X AKR/J offspring indicated that this B cell marker was not linked to geneslambdacoding for H-2.31 or Ly 4.2. The C57BL/Ks anti-L1210 serum identified a new polymorphic genetic locus, the product of which was B lymphocyte specific.
L1210小鼠淋巴母细胞系具有一种B淋巴细胞特异性同种抗原,该抗原可用C57BL/Ks抗L1210血清检测到。在脾B淋巴细胞上发现了该抗原,但在胸腺细胞、T淋巴细胞或红细胞上未发现。它仅存在于7%的骨髓细胞中。C57BL/Ks抗DBA/2脾血清的反应性与抗L1210血清的反应性无法区分,这证实该抗原是CBA/2小鼠B淋巴细胞的正常成分。C57BL/Ks抗L1210血清检测到的该抗原的品系分布模式表明,这种同种抗原不是H-2K、H-2D、Mls或Ig基因座的等位基因。遗传分析表明,该抗原作为单一孟德尔显性性状遗传。(B10.BR×DBA/2)F1×AKR/J后代的分离分析表明,这种B细胞标记物与编码H-2.31或Ly 4.2的基因不连锁。C57BL/Ks抗L1210血清鉴定出一个新的多态性遗传位点,其产物是B淋巴细胞特异性的。