Bieberich C, Yoshioka T, Tanaka K, Jay G, Scangos G
Department of Biology, Johns Hopkins University, Baltimore, Maryland 21218.
Mol Cell Biol. 1987 Nov;7(11):4003-9. doi: 10.1128/mcb.7.11.4003-4009.1987.
The regulated expression of major histocompatibility complex class I antigens is essential for assuring proper cellular immune responses. To study H-2 class I gene regulation, we have transferred a foreign class I gene to inbred mice and have previously shown that the heterologous class I gene was expressed in a tissue-dependent manner. In this report, we demonstrate that these mice expressed the transgenic class I molecule on the cell surface without any alteration in the level of endogenous H-2 class I antigens. Skin grafts from transgenic mice were rapidly rejected by mice of the background strain, indicating that the transgenic antigen was expressed in an immunologically functional form. As with endogenous H-2 class I genes, the class I transgene was inducible by interferon treatment and suppressible by human adenovirus 12 transformation. Linkage analysis indicated that the transgene was not closely linked to endogenous class I loci, suggesting that trans-regulation of class I genes can occur for class I genes located outside the major histocompatibility complex.
主要组织相容性复合体I类抗原的调控表达对于确保适当的细胞免疫反应至关重要。为了研究H-2 I类基因调控,我们已将一个外源I类基因转移到近交系小鼠中,并且先前已表明异源I类基因以组织依赖性方式表达。在本报告中,我们证明这些小鼠在细胞表面表达转基因I类分子,而内源性H-2 I类抗原水平没有任何改变。转基因小鼠的皮肤移植被背景品系的小鼠迅速排斥,表明转基因抗原以免疫功能形式表达。与内源性H-2 I类基因一样,I类转基因可通过干扰素处理诱导,并可被人腺病毒12转化抑制。连锁分析表明,转基因与内源性I类基因座没有紧密连锁,这表明对于位于主要组织相容性复合体外的I类基因,I类基因的反式调控可能会发生。