CD40 ligation impedes lymphoblastoid B cell proliferation and S-phase entry

被引:7
作者
Bishop, JY
Schattner, EJ
Friedman, SM
机构
[1] Hosp Special Surg, Div Rheumatol, New York, NY 10021 USA
[2] Cornell Univ, Coll Med, Program Mol Med, New York, NY USA
[3] New York Hosp, Dept Med, Div Hematol Oncol, New York, NY 10021 USA
关键词
lymphoma; B cells; cell cycle; CD40; growth inhibition;
D O I
10.1016/S0145-2126(97)00173-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The CD40 cell surface antigen and member of the tumor necrosis factor (TNF) receptor superfamily is expressed in many cell types, including normal and neoplastic B cells. Signaling through CD40 induces B cell proliferation, differentiation and, in some circumstances, protects the B cell from apoptosis. Lymphoblastoid cells (LCLs) resemble the malignant B cells that comprise the Epstein-Barr virus (EBV)-associated posttransplant lymphoproliferative disorders, in that the cells bear a highly activated phenotype and, unlike most other EBV positive tumor cells, express the majority of latent EBV genes. In this study, we use assays of cell viability, proliferation, cell cycle and apoptosis to demonstrate that ligation of the CD40 receptor in EBV-transformed LCLs inhibits their growth. The process does not involve apoptosis, but is characterized by reduced S-phase entry from G(O)/G(I). A better understanding of the negative effects of CD40 ligation in these cells may offer clues for the development of novel therapies in EBV-related B cell disorders. (C) 1998 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:319 / 327
页数:9
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