Meco D, Scarpa S, Napolitano M, Maroder M, Bellavia D, De Maria R, Ragano-Caracciolo M, Frati L, Modesti A, Gulino A
Department of Experimental Medicine, University La Sapienza, Rome, Italy.
J Immunol. 1994 Jul 1;153(1):73-83.
Retinoic acid (RA) controls the differentiation of a variety of cell types, although its role in influencing T cell development and the mechanisms potentially involved have not been thoroughly investigated. To study the ability of RA to modulate T cell development, we established a thymic stromal cell line (TC-1S) that supports the phenotypic maturation of CD4-8- double negative (DN) or CD3-4-8- triple negative (TN) thymocyte precursors. Cocultures of either DN or TN thymocytes on a monolayer of TC-1S cells resulted in the appearance of thymocytes with a more mature phenotype (CD4+8+ double positive, CD4+ or CD8+ single positive, and CD3(low) cells). Double negative T cell contact with TC-1S cells also increased the production of fibronectin (FN) by the thymic stroma and the expression of the VLA-4 FN receptor on the DN cells. Ab-mediated inhibition of the interaction between FN and its receptors significantly reduced the level of induced T cell maturation. Addition of RA either to TC-1S cells alone or to the coculture with DN cells decreased stromal cell FN expression, antagonized DN cell-induced increase in stromal cell FN production and significantly inhibited in vitro thymocyte maturation. The effects of RA were likely mediated by RA acid receptors alpha and gamma expressed both in DN thymocytes and TC-1S cells. Together these data suggest that FN/VLA-4 interaction may be an important component of stromal cell-dependent thymocyte phenotypic differentiation and that this interaction can be one of the targets for the influence of RA in T cell development.
视黄酸(RA)可控制多种细胞类型的分化,尽管其在影响T细胞发育方面的作用以及潜在机制尚未得到充分研究。为了研究RA调节T细胞发育的能力,我们建立了一种胸腺基质细胞系(TC-1S),它能支持CD4-8-双阴性(DN)或CD3-4-8-三阴性(TN)胸腺细胞前体的表型成熟。将DN或TN胸腺细胞与TC-1S细胞单层共培养,会导致出现具有更成熟表型的胸腺细胞(CD4+8+双阳性、CD4+或CD8+单阳性以及CD3(低表达)细胞)。双阴性T细胞与TC-1S细胞的接触还增加了胸腺基质中纤连蛋白(FN)的产生以及DN细胞上VLA-4 FN受体的表达。抗体介导的对FN与其受体之间相互作用的抑制显著降低了诱导的T细胞成熟水平。单独向TC-1S细胞或与DN细胞共培养物中添加RA,会降低基质细胞FN表达,拮抗DN细胞诱导的基质细胞FN产生增加,并显著抑制体外胸腺细胞成熟。RA的作用可能是由在DN胸腺细胞和TC-1S细胞中均表达的视黄酸受体α和γ介导的。这些数据共同表明,FN/VLA-4相互作用可能是基质细胞依赖性胸腺细胞表型分化的重要组成部分,并且这种相互作用可能是RA影响T细胞发育的靶点之一。