Characterization of a cell surface-expressed disulfide-linked dimer involved in murine T cell activation.

作者：W M Yokoyama, Frits Koning, Patricia J. Kehn, Geraldo M. B. Pereira, George Stingl, John E. Coligan, Ethan M. Shevach · 发表于：The Journal of Immunology · 年份：1988 · DOI：10.4049/jimmunol.141.2.369 · 被引用次数：157 · 研究领域：Monoclonal and Polyclonal Antibodies Research、Ubiquitin and proteasome pathways、Glycosylation and Glycoproteins Research

We have produced a hamster mAb, H1.2F3, which was derived by immunization with a murine TCR-gamma delta + epidermal T cell line. H1.2F3 immunoprecipitates a cell surface-expressed disulfide-linked dimer that has a m.w. of 85,000 under non-reducing conditions and consists of subunits of 35,000 to 39,000 m.w. This dimer is distinct from the CD3-associated TCR-gamma delta complex (CD3/TCR), inasmuch as H1.2F3 does not co-precipitate or co-modulate with the CD3/TCR complex and recognizes an Ag with a single-peptide backbone of 22,000 m.w. after N-Glycanase treatment. H1.2F3 is weakly reactive with a small percentage of cells from unfractionated thymus, spleen, or lymph node, but reactivity with both T and B lymphocytes is markedly enhanced by a brief period of stimulation with Con A or PMA in vitro. This enhancement requires de novo protein synthesis. Enhanced expression of the H1.2F3 Ag can also be induced in vivo by injection of Con A or anti-CD3. H1.2F3 is a potent stimulator of T, but not B, cell proliferation in the presence of PMA and FcR-bearing accessory cells. These functional and biochemical studies strongly suggest that the Ag recognized by H1.2F3 is the murine homologue of the human CD28 Ag recognized by mAb 9.3.