Salomon D R, Mojcik C F, Chang A C, Wadsworth S, Adams D H, Coligan J E, Shevach E M
Laboratory of Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892.
J Exp Med. 1994 May 1;179(5):1573-84. doi: 10.1084/jem.179.5.1573.
Our understanding of thymocyte development and of the positive and negative selection events involved in shaping the repertoire of mature T lymphocytes has been greatly facilitated by the use of transgenic and gene knockout animals. Much less is known about the factors that control the homing and population of the thymus by T cell precursors and the subsequent migration of developing thymocytes through the thymic architecture. As the integrins represent a candidate group of cell surface receptors that may regulate thymocyte development, we have analyzed the expression and function of alpha 4 beta 1 and alpha 5 beta 1 on human thymocytes. A major portion of double positive (CD4+ CD8+) human thymocytes express alpha 4 beta 1 in a constitutively active form and adhere to fibronectin and vascular cell adhesion molecule 1. alpha 4 beta 1 expression is similar on adherent and nonadherent populations, thus, activity reflects the receptor state and not simple expression. The adherent cells are immature, expressing high levels of CD4/CD8 and low levels of CD3 and CD69. In contrast, nonadherent cells possess the phenotype of thymocytes after positive selection, expressing intermediate levels of CD4 and/or CD8 and high levels of CD3 and CD69. The adherent population fails to respond to activation with anti-CD3 and fibronectin, whereas nonadherents exhibit an alpha 5 beta 1-dependent proliferation. Differential regulation of alpha 4 beta 1 and alpha 5 beta 1 receptors may provide a mechanism controlling cellular traffic, differentiation, and positive selection of thymocytes.
利用转基因动物和基因敲除动物极大地促进了我们对胸腺细胞发育以及成熟T淋巴细胞库形成过程中涉及的阳性和阴性选择事件的理解。对于控制T细胞前体归巢至胸腺以及胸腺细胞随后通过胸腺结构迁移的因素,我们了解得还很少。由于整合素是可能调节胸腺细胞发育的一类候选细胞表面受体,我们分析了α4β1和α5β1在人胸腺细胞上的表达和功能。大部分双阳性(CD4+CD8+)人胸腺细胞以组成性激活形式表达α4β1,并黏附于纤连蛋白和血管细胞黏附分子1。α4β1在黏附细胞群和非黏附细胞群中的表达相似,因此,活性反映的是受体状态而非简单的表达情况。黏附细胞不成熟,高水平表达CD4/CD8,低水平表达CD3和CD69。相反,非黏附细胞具有阳性选择后胸腺细胞的表型,表达中等水平的CD4和/或CD8以及高水平的CD3和CD69。黏附细胞群对用抗CD3和纤连蛋白激活无反应,而非黏附细胞表现出α5β1依赖性增殖。α4β1和α5β1受体的差异调节可能提供一种控制胸腺细胞细胞运输、分化和阳性选择的机制。