Ge Qing, Stone Jennifer D, Thompson M Todd, Cochran Jennifer R, Rushe Mia, Eisen Herman N, Chen Jianzhu, Stern Lawrence J
Department of Biology, Center for Cancer Research, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Proc Natl Acad Sci U S A. 2002 Oct 15;99(21):13729-34. doi: 10.1073/pnas.212515299. Epub 2002 Oct 8.
T cell receptor (TCR)-mediated activation of CD4(+) T cells is known to require multivalent engagement of the TCR by, for example, oligomeric peptide-MHC complexes. In contrast, for CD8(+) T cells, there is evidence for TCR-mediated activation by univalent engagement of the TCR. We have here compared oligomeric and monomeric L(d) and K(b) peptide-MHC complexes and free peptide as stimulators of CD8(+) T cells expressing the 2C TCR. We found that the monomers are indeed effective in activating naive and effector CD8(+) T cells, but through an unexpected mechanism that involves transfer of peptide from soluble monomers to T cell endogenous MHC (K(b)) molecules. The result is that T cells, acting as antigen-presenting cells, are able to activate other naive T cells.
已知T细胞受体(TCR)介导的CD4(+) T细胞活化需要TCR通过多价结合,例如通过寡聚肽-MHC复合物来实现。相比之下,对于CD8(+) T细胞,有证据表明TCR通过单价结合即可介导活化。我们在此比较了寡聚体和单体形式的L(d)和K(b)肽-MHC复合物以及游离肽作为表达2C TCR的CD8(+) T细胞刺激物的情况。我们发现单体确实能够有效激活初始和效应CD8(+) T细胞,但通过一种意想不到的机制,该机制涉及肽从可溶性单体转移至T细胞内源性MHC(K(b))分子。结果是,作为抗原呈递细胞的T细胞能够激活其他初始T细胞。