CD2 ligation abrogates antigen-independent apoptosis in B cells

被引:3
作者
Baixeras, E
Moreno, MC
MartinezA, C
机构
[1] Ctro. Nac. de Biotecnologia, Univ. Autónoma de Madrid, Campus de Cantoblanco
关键词
D O I
10.1006/cimm.1996.0172
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We have described recently the prevention of apoptosis by CDS-soluble CD48 interaction on antigen B cell receptor occupancy. Here, we show that CD2 ligation is also able to interfere with B cell receptor-independent apoptosis pathways such as spontaneous death in spleen B cells or serum deprivation and hydrogen peroxide exposure in the BAL-17 cell line. In all cases, CD2 ligation induces a signal that prevents the downregulation of Bcl-2 expression. The specific CD2 signal pathway involved in this phenomenon is still unknown. As reported, CD2 did not appear to induce Ca2+ mobilization, phosphatidylinositol turnover, or PKC translocation in B cells. Nevertheless, we show that CD2 receptor ligation is coupled to the tyrosine phosphorylation pathway in B cells. These observations indicate that CD2 is functionally able to trigger at least an early signal that could play a role in apoptosis blockage B cells in addition to the adhesion one. The results suggest the participation of cellular membrane receptors other that CD40 in apoptosis rescue, not only in the antigen-dependent but also in the antigen-independent phases of B cell lymphopoiesis. (C) 1996 Academic Press, Inc.
引用
收藏
页码:55 / 61
页数:7
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