Department of Microbiology and Immunology, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, USA.
Immunogenetics. 2010 Feb;62(2):109-16. doi: 10.1007/s00251-009-0418-3. Epub 2009 Dec 19.
Loss of major histocompatibility complex class II (MHCII) antigen expression on diffuse large B cell lymphoma (DLBCL) corresponds closely with significant decreases in patient survival. However, the mechanisms accounting for MHCII loss in DLBCL have not been thoroughly characterized to date. In this report, we demonstrate that coordinate loss of MHCII expression in OCI-Ly2 DLBCL cells is associated with an 11-base deletion in the cDNA encoding RFX-AP, one of the subunits of the heterotrimeric regulatory factor X (RFX) that is required for activating MHCII transcription. This deletion results in a frameshift in the RFX-AP protein beginning at amino acid 234 and, therefore, in the loss of C-terminal amino acids that are required for function. Stable transfection of OCI-Ly2 DLBCL cells with an expression vector for wild-type RFX-AP restores MHCII expression, which strongly suggests that the defect in RFX-AP accounts for MHCII loss in these cells.
弥漫性大 B 细胞淋巴瘤 (DLBCL) 中主要组织相容性复合体 II (MHCII) 抗原表达的丧失与患者生存的显著降低密切相关。然而,迄今为止,尚不清楚导致 DLBCL 中 MHCII 丧失的机制。在本报告中,我们证明了 OCI-Ly2 DLBCL 细胞中 MHCII 表达的协同丧失与编码 RFX-AP 的 cDNA 中 11 个碱基对的缺失有关,RFX-AP 是异源三聚体调节因子 X (RFX) 的亚基之一,对于 MHCII 转录的激活是必需的。这种缺失导致 RFX-AP 蛋白在氨基酸 234 处发生移码,因此,丧失了功能所必需的 C 末端氨基酸。用野生型 RFX-AP 的表达载体稳定转染 OCI-Ly2 DLBCL 细胞可恢复 MHCII 的表达,这强烈表明 RFX-AP 的缺陷导致了这些细胞中 MHCII 的丧失。