CD22-MEDIATED STIMULATION OF T-CELLS REGULATES T-CELL RECEPTOR CD3-INDUCED SIGNALING

被引:99
作者
ARUFFO, A
KANNER, SB
SGROI, D
LEDBETTER, JA
STAMENKOVIC, I
机构
[1] MASSACHUSETTS GEN HOSP,DEPT PATHOL,MGH E,BLDG 149,13TH ST,BOSTON,MA 02129
[2] PATHOL RES,BOSTON,MA 02129
[3] BRISTOL MYERS SQUIBB PHARMACEUT RES INST,SEATTLE,WA 98121
[4] HARVARD UNIV,SCH MED,BOSTON,MA 02129
关键词
CD22; CD45; SIALIC ACID; CARBOHYDRATE; ADHESION;
D O I
10.1073/pnas.89.21.10242
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Interaction between B lymphocytes and other cell types is mediated in part by the B-cell adhesion molecule CD22. Recent work has suggested one of the T-cell ligands of B cells to be CD45RO, an isoform of the receptor-linked phosphotyrosine phosphatase CD45. Here we demonstrate direct interaction between CD22 and several isoforms of CD45, including CD45RO, and propose that the interaction may participate in regulation of lymphocyte signaling. Cross-linking of CD3 and CD22 T-cell ligands with anti-CD3 antibody and soluble CD22 is shown to block anti-CD3-induced intracellular calcium increase and to inhibit tyrosine phosphorylation of phospholipase Cgamma1. These effects are consistent with those observed upon coligation of CD3 and CD45 with antibody, providing support to the possibility that ligand-mediated stimulation of CD45 may result in modulation of substrate phosphorylation and lymphocyte activation.
引用
收藏
页码:10242 / 10246
页数:5
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