Utsumi K, Sawada M, Narumiya S, Nagamine J, Sakata T, Iwagami S, Kita Y, Teraoka H, Hirano H, Ogata M
Biomedical Research Center, Osaka University Medical School, Japan.
Proc Natl Acad Sci U S A. 1991 Jul 1;88(13):5685-9. doi: 10.1073/pnas.88.13.5685.
Only 10-15% of unseparated thymocytes adhered to culture plates precoated with fibronectin (FN), but 60-70% of the CD4-8- (double-negative) thymocyte population did. This population bound to FN but not to collagen, laminin, or vitronectin. Its binding to FN was inhibited by anti-FN antibody or a mixture of synthetic peptides corresponding to two different sites of FN, termed the V10 sequence and the RGDS (Arg-Gly-Asp-Ser) sequence, which interact, respectively, with the VLA-4 and VLA-5 FN receptors expressed on T-lineage cells. CD4-8- thymocytes also adhered to a monolayer of a thymic stromal cell clone, MRL104.8a, that induces growth-maintenance and differentiation of such thymocytes. The involvement of FN-FN receptor interaction in this adhesion was demonstrated by the following lines of evidence: (i) the MRL104.8a cells expressed FN molecules on their surface and (ii) the adhesion of CD4-8- thymocytes to MRL104.8a monolayers was almost completely inhibited by simultaneous addition of anti-FN antibody and a mixture of peptides (V10 plus RGDS) capable of binding to anti-FN receptors (VLA-4 and -5). Most important, blocking the adhesion of CD4-8- thymocytes to the thymic stromal cell monolayer resulted in potent inhibition of the differentiation of these thymocytes, which was otherwise induced toward the expression of CD4 and/or CD8 molecules. These results indicate that immature CD4-8- thymocytes adhere to thymic stromal cells preferentially through FN-FN receptor interaction and that such adhesion has a critical role in inducing and/or supporting the differentiation of these thymocytes.
未分离的胸腺细胞中只有10 - 15%能黏附于预先包被纤连蛋白(FN)的培养板,但CD4 - 8 - (双阴性)胸腺细胞群体中有60 - 70%能黏附。该群体与FN结合,但不与胶原蛋白、层粘连蛋白或玻连蛋白结合。其与FN的结合被抗FN抗体或对应于FN两个不同位点的合成肽混合物抑制,这两个位点分别称为V10序列和RGDS(精氨酸 - 甘氨酸 - 天冬氨酸 - 丝氨酸)序列,它们分别与T细胞谱系细胞上表达的VLA - 4和VLA - 5 FN受体相互作用。CD4 - 8 - 胸腺细胞也能黏附于胸腺基质细胞克隆MRL104.8a的单层细胞,该克隆可诱导此类胸腺细胞的生长维持和分化。以下一系列证据证明了FN - FN受体相互作用参与了这种黏附:(i)MRL104.8a细胞在其表面表达FN分子;(ii)同时添加抗FN抗体和能够结合抗FN受体(VLA - 4和 - 5)的肽混合物(V10加RGDS)几乎完全抑制了CD4 - 8 - 胸腺细胞与MRL104.8a单层细胞的黏附。最重要的是,阻断CD4 - 8 - 胸腺细胞与胸腺基质细胞单层的黏附会导致这些胸腺细胞分化的有效抑制,否则这些胸腺细胞会被诱导表达CD4和/或CD8分子。这些结果表明,未成熟的CD4 - 8 - 胸腺细胞优先通过FN - FN受体相互作用黏附于胸腺基质细胞,并且这种黏附在诱导和/或支持这些胸腺细胞的分化中起关键作用。