Soloski M J, Vernachio J, Einhorn G, Lattimore A
Proc Natl Acad Sci U S A. 1986 May;83(9):2949-53. doi: 10.1073/pnas.83.9.2949.
The biosynthesis and expression of the tissue-specific class I molecule Qa-2 have been studied in resting and activated T-cell populations. Polyclonal activation of T lymphocytes induces a 3- to 4-fold increase in the biosynthesis of Qa-2 molecules but no increase in cell-surface levels. Analysis of the biosynthetic pathway of the Qa-2 molecule in activated lymphocytes reveals that approximately equal to 70% of the newly synthesized Qa-2 molecules are secreted as soluble molecules. In resting-cell populations, Qa-2 remains entirely cell-associated. This process is unique to the Qa-2 molecule, since other class I molecules (e.g., H-2Kb and H-2Db) synthesized by activated cells remain cell-associated. The possibility that the secreted Qa-2 molecule is the product of a new Qa gene or an alternatively spliced mRNA is considered. These results indicate that the Qa-2 molecules may not just function as a cell-surface recognition structure but also may serve a role as a soluble factor synthesized by activated lymphoid cell populations.
在静止和活化的T细胞群体中,对组织特异性I类分子Qa-2的生物合成及表达进行了研究。T淋巴细胞的多克隆激活会使Qa-2分子的生物合成增加3至4倍,但细胞表面水平并未升高。对活化淋巴细胞中Qa-2分子生物合成途径的分析表明,新合成的Qa-2分子中约70%作为可溶性分子被分泌。在静止细胞群体中,Qa-2完全与细胞相关。这一过程是Qa-2分子所特有的,因为活化细胞合成的其他I类分子(如H-2Kb和H-2Db)仍与细胞相关。研究了分泌的Qa-2分子是新的Qa基因产物或可变剪接mRNA产物的可能性。这些结果表明,Qa-2分子可能不仅作为细胞表面识别结构发挥作用,还可能作为活化淋巴细胞群体合成的可溶性因子发挥作用。