Hogarth P M, Crewther P E, McKenzie I F
Eur J Immunol. 1982 May;12(5):374-9. doi: 10.1002/eji.1830120504.
Several new aspects of the chemistry, genetics and cellular distribution of the murine Qa-2 alloantigen were apparent in an analysis of this antigen using monoclonal antibodies recognizing a Qa-2-like antigen called Qa-m2. Immunoprecipitation and sodium dodecyl sulfate polyacrylamide gel electrophoresis analysis identified the Qa-m2 alloantigen as a two-chain structure composed of a 39 000 dalton heavy chain and a 12 000 light chain which is probably beta 2-microglobulin; the heavy chain was readily distinguished from that of H-2. In addition, the expression of Qa-m2 alloantigens on the cell surface was found to be controlled by the H-2D gen with H-2Db strains carrying approximately 8-10 times greater amounts of Qa-m2 than strains carrying the H-2Dd or H-2Dq alleles. Finally, the Qa-m2 antigen, found predominantly on peripheral T cells, was present on only 10% of thymus cells. However, subpopulations of B cells (approximately 25% of all B cells) and bone marrow cells (15-20%) were also reactive. The monoclonal anti-Qa-m2 antibodies differed in their reactions from that reported for the conventional anti-Qa-2 sera, which must, therefore, be complex. The monoclonal antibodies may be useful reagents for functional analysis of T and B cell subpopulations.
在使用识别一种名为Qa-m2的类Qa-2抗原的单克隆抗体对小鼠Qa-2同种抗原进行分析时,该抗原在化学、遗传学和细胞分布方面的几个新情况变得明显。免疫沉淀和十二烷基硫酸钠聚丙烯酰胺凝胶电泳分析将Qa-m2同种抗原鉴定为一种由39000道尔顿重链和12000轻链(可能是β2-微球蛋白)组成的双链结构;重链很容易与H-2的重链区分开来。此外,发现细胞表面Qa-m2同种抗原的表达受H-2D基因控制,携带H-2Db等位基因的品系所携带的Qa-m2量比携带H-2Dd或H-2Dq等位基因的品系多大约8 - 10倍。最后,主要在外周T细胞上发现的Qa-m2抗原仅存在于10%的胸腺细胞上。然而,B细胞亚群(约占所有B细胞的25%)和骨髓细胞(15 - 20%)也有反应。单克隆抗Qa-m2抗体的反应与报道的传统抗Qa-2血清的反应不同,因此传统抗血清必定很复杂。单克隆抗体可能是用于T和B细胞亚群功能分析的有用试剂。