Dickles H B, Ahmed A, Sachs D H
J Exp Med. 1977 Dec 1;146(6):1678-92. doi: 10.1084/jem.146.6.1678.
Certain non-H-2 alloantigens are associated with murine B-lymphocyte Fc receptors in that pretreatment of spleen cells with alloantibodies against these antigens inhibited binding of Ig complexes to B-cell Fc receptors. This inhibition was specific in that: (a) as has been shown previously, the Fc portion of the alloantibody was not required to produce inhibition; and (b) antibodies against some non-H-2 antigens but not antibodies against others (including some that were expressed on B cells) caused such inhibition. Backcross experiments revealed that the B-cell Fc receptor-associated non-H-2 antigens were determined by the gene(s) of a single background locus in each of the three strains tested (A/J, B10, and CBA/J). This locus was poly-morphic in that at least four different B-cell Fc receptor:associated non-H-2 antigens were identified (one each in the A/J, B10, and CBAJJ and one antigen shared or crossreactive between the B10 and CBA/J). These antigens were primarily but not exclusively expressed on B lymphocytes as determined by immunofluorescence studies, and on the basis of capping experiments they did not appear to be identical to B-cell Fc receptors. Linkage studies revealed that the locus which determined these antigens was not linked to the albino locus nor the heavy chain allotype locus and expression was neither sex-limited nor an X-linked recessive trait. However, this locus was closely linked but not identical to the Mls locus (apparent recombination frequency 6.8 percent). Thus, two closely linked non-H-2 loci both determine the expression of antigens which have characteristics similar to Ia antigens. One locus is polymorphic and determines the expression of antigens which are primarily expressed on B cells and are specifically associated with the Fc receptors of these cells. The other (Mls locus) determines antigens which are stimulatory in mixed lymphocyte cultures. These observations suggest that there may be a second gene complex which is the analogue of the I region of the H-2 complex.
某些非H-2同种抗原与鼠B淋巴细胞Fc受体相关,因为用针对这些抗原的同种抗体预处理脾细胞可抑制Ig复合物与B细胞Fc受体的结合。这种抑制具有特异性,具体表现为:(a) 如先前所示,产生抑制作用不需要同种抗体的Fc部分;(b) 针对某些非H-2抗原的抗体可导致这种抑制,而针对其他抗原(包括一些在B细胞上表达的抗原)的抗体则不会。回交实验表明,在测试的三个品系(A/J、B10和CBA/J)中,B细胞Fc受体相关的非H-2抗原由单个背景基因座的基因决定。该基因座具有多态性,因为至少鉴定出四种不同的B细胞Fc受体相关非H-2抗原(A/J、B10和CBA/J各一种,以及B10和CBA/J之间共享或交叉反应的一种抗原)。免疫荧光研究表明,这些抗原主要但并非仅在B淋巴细胞上表达,基于封帽实验,它们似乎与B细胞Fc受体不同。连锁研究表明,决定这些抗原的基因座与白化病基因座和重链同种异型基因座均无连锁关系,其表达既不受性别限制,也不是X连锁隐性性状。然而,该基因座与Mls基因座紧密连锁但并不相同(明显重组频率为6.8%)。因此,两个紧密连锁的非H-2基因座均决定具有与Ia抗原相似特征的抗原表达。一个基因座具有多态性,决定主要在B细胞上表达并与这些细胞的Fc受体特异性相关的抗原表达。另一个(Mls基因座)决定在混合淋巴细胞培养中具有刺激作用的抗原。这些观察结果表明,可能存在第二个基因复合体,它是H-2复合体I区的类似物。