Convergence between CD98 and integrin-mediated T-lymphocyte co-stimulation

被引:29
作者
Warren, AP
Patel, K
Miyamoto, Y
Wygant, JN
Woodside, DG
McIntyre, BW
机构
[1] St George Hosp, Sch Med, Dept Biochem, London SW17 0RE, England
[2] United Med & Dent Sch, Div Physiol, London, England
[3] Univ Texas, MD Anderson Canc Ctr, Dept Immunol, Houston, TX 77030 USA
关键词
D O I
10.1046/j.1365-2567.2000.00953.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CD98 is a widely expressed cell surface heterodimeric glycoprotein, which is rapidly up-regulated upon activation of T lymphocytes. Monoclonal antibody (mAb) 80A10 recognizes an epitope on CD98 and in combination with CD3 antibody causes proliferation of peripheral blood T lymphocytes. CD98 co-stimulatory activity, mediated by either mAb 80A10 or 4F2, a well-characterized CD98-specific mAb, is blocked in the presence of the soluble beta 1 integrin antibody 18D3. Previously we have reported that co-stimulatory activity of antibodies to integrins alpha(4)beta(1), alpha(5)beta(1), alpha(L)beta(2) and alpha(4)beta(7) is inhibited by 18D3, whereas co-stimulation mediated by non-integrins was unaffected. Thus the non-integrin CD98 is uniquely sensitive to the inhibitory effects of beta(1) integrin-blocking antibodies, which may reflect convergent signalling mechanisms between integrins and CD98. This is consistent with recent reports suggesting that CD98 may regulate integrin-mediated adhesive events.
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页码:62 / 68
页数:7
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