Reversal of EBV immortalization precedes apoptosis in IL-6-induced human B cell terminal differentiation

被引:52
作者
Altmeyer, A
Simmons, RC
Krajewski, S
Reed, JC
Bornkamm, GW
ChenKiang, S
机构
[1] CORNELL UNIV,COLL MED,DEPT PATHOL,NEW YORK,NY 10021
[2] CORNELL UNIV,COLL MED,DEPT MICROBIOL,NEW YORK,NY 10021
[3] BURNHAM INST,LA JOLLA,CA 92037
[4] INST KLIN MOL BIOL & TUMOR GENET,HAMATOLOGIKUM,D-81377 MUNICH,GERMANY
关键词
D O I
10.1016/S1074-7613(00)80387-8
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cell death in B cell terminal differentiation rapidly follows cell cycle arrest in IL-6 differentiation of EBV-immortalized, lgG-bearing human lymphoblastoid cells in vitro. G1 arrest is now found to coincide with repression of EBNA2 and LMP1, two EBV genes essential for B cell transformation, without activation of the viral lytic cycle. IL-6-differentiated B cells die by apoptosis, as evidenced by increases in Annexin V binding activity, PARP cleavage, and chromatin disorganization. Expression of Mcl-1, a Bcl-2 family member, was specifically induced during IL-6 differentiation and downregulated during apoptosis. Thus, IL-6 reverses EBV immortalization and activates the terminal differentiation program in IgG-bearing human B lymphoblastoid cells, including regulation of an anti-apoptotic gene to coordinate differentiation, cell cycle arrest, and cell death.
引用
收藏
页码:667 / 677
页数:11
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