Salter R D, Alexander J, Levine F, Pious D, Cresswell P
J Immunol. 1985 Dec;135(6):4235-8.
Previous studies have shown that a trans-acting regulatory factor is required for expression of HLA class II molecules in B-LCL, and that a trans-active factor derived from B-LCL induces de novo synthesis of T-LCL-encoded class II antigens in hybrids of T-LCL and B-LCL. To further examine the genetics of class II antigen regulation, we have now fused two different T-LCL with the class II antigen negative B-LCL 6.1.6, a regulatory mutant that does not synthesize a trans-acting factor necessary for transcription of class II genes. Northern blot analysis and cell surface immunofluorescence studies indicate that the hybrids express class II antigens encoded by both 6.1.6 and T-LCL parent cell lines. Thus, expression of class II antigens in these hybrids is controlled by a minimum of two trans-acting regulatory genes. One of these genes is inactivated in the 6.1.6 mutant and is provided by the T-LCL fusion partner. The second regulatory gene may still be active in 6.1.6, but it alone is insufficient for maintenance of class II antigen expression.
先前的研究表明,B淋巴母细胞样细胞系(B-LCL)中HLA II类分子的表达需要一种反式作用调节因子,并且来自B-LCL的反式激活因子可在T淋巴母细胞样细胞系(T-LCL)与B-LCL的杂交细胞中诱导T-LCL编码的II类抗原的从头合成。为了进一步研究II类抗原调节的遗传学,我们现在将两种不同的T-LCL与II类抗原阴性的B-LCL 6.1.6进行融合,B-LCL 6.1.6是一种调节突变体,不合成II类基因转录所需的反式作用因子。Northern印迹分析和细胞表面免疫荧光研究表明,杂交细胞表达由6.1.6和T-LCL亲代细胞系编码的II类抗原。因此,这些杂交细胞中II类抗原的表达至少受两个反式作用调节基因的控制。其中一个基因在6.1.6突变体中失活,并由T-LCL融合伴侣提供。第二个调节基因在6.1.6中可能仍然活跃,但仅靠它不足以维持II类抗原的表达。