Peng-Pilon M, Ruuth K, Lundgren E, Brodin P
Department of Cell and Molecular Biology, University of Umea, Sweden.
J Gen Virol. 1995 Apr;76 ( Pt 4):767-77. doi: 10.1099/0022-1317-76-4-767.
The Epstein-Barr virus (EBV) latent membrane protein 1 (LMP-1) is essential for EBV-induced immortalization of human primary B cells, transforms rodent fibroblasts and induces the up-regulation of several B cell activation markers when transiently expressed in primary B cells. The biochemical function of LMP-1 is unclear and limited information is available on the involvement of different domains of the protein in B cell activation. The present study describes the characterization of LMP-1 N- and C-terminal deletion mutants in terms of their cell surface distribution and ability to induce activation markers in primary human B cells and in the type I Burkitt's lymphoma cell line DG75. The C-terminal deletion mutant was detected by immunofluorescence via antibodies targeted against an eight amino acid FLAG epitope substituted for the entire predicted cytoplasmic C-terminal domain. Our findings show that N-terminal deletion mutants of LMP-1 are unable to attain their usual patched distribution on the plasma membrane but retain the ability to activate B cells. In contrast, the C-terminal deletion mutant shows the same patched cell surface distribution as wild-type LMP-1 but is unable to activate B cells. The patched distribution of LMP-1 in the plasma membrane is therefore not sufficient nor necessary for the induction of B cell activation and the results rule out patching as a direct mechanism in LMP-1-induced activation. This is the first study addressing the role of the LMP-1 C-terminal domain in lymphocytes and our results show that this domain is essential for B cell activation and therefore likely to be important for the early events of B cell immortalization by EBV.
爱泼斯坦-巴尔病毒(EBV)潜伏膜蛋白1(LMP-1)对于EBV诱导人原代B细胞永生化至关重要,可转化啮齿动物成纤维细胞,并在原代B细胞中瞬时表达时诱导多种B细胞活化标志物上调。LMP-1的生化功能尚不清楚,关于该蛋白不同结构域参与B细胞活化的信息有限。本研究描述了LMP-1 N端和C端缺失突变体在原代人B细胞和I型伯基特淋巴瘤细胞系DG75中的细胞表面分布及其诱导活化标志物的能力。通过针对替代整个预测胞质C端结构域的八氨基酸FLAG表位的抗体,通过免疫荧光检测C端缺失突变体。我们的研究结果表明,LMP-1的N端缺失突变体无法在质膜上获得其通常的斑块状分布,但保留了激活B细胞的能力。相反,C端缺失突变体显示出与野生型LMP-1相同的斑块状细胞表面分布,但无法激活B细胞。因此,LMP-1在质膜上的斑块状分布对于诱导B细胞活化既不充分也不必要,结果排除了斑块形成作为LMP-1诱导活化的直接机制。这是第一项研究LMP-1 C端结构域在淋巴细胞中作用的研究,我们的结果表明该结构域对于B细胞活化至关重要,因此可能对EBV使B细胞永生化的早期事件很重要。