Lannes-Vieira J, Chammas R, Villa-Verde D M, Vannier-dos-Santos M A, Mello-Coelho V, de Souza S J, Brentani R R, Savino W
Department of Immunology, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil.
Int Immunol. 1993 Nov;5(11):1421-30. doi: 10.1093/intimm/5.11.1421.
We describe herein the expression of the VLA6 complex by murine thymic epithelial cells (TEC). The immunohistochemical distribution revealed that VLA6 is found in both thymic medullary and subcapsullary areas. Moreover, studies by immunoelectron microscopy revealed a membrane labeling of the VLA6 molecule, including at desmosomal sites. By means of immunoblotting, immunoprecipitation, and affinity chromatography of extracts from a mouse TEC line, we further demonstrated that VLA6 is a laminin (LN) receptor in these cells. In keeping with this finding, we showed that TEC adhesion, spreading, and proliferation were enhanced in vitro by LN. The fact that VLA6 is also expressed by the large majority of thymocytes raised the hypothesis that it might be involved in LN-mediated TEC-thymocyte interactions. Interestingly, in vitro experiments showed that there is an increase in the TEC-thymocyte adhesion upon glucocorticoid hormone treatment, a situation in which the expression of VLA6 as well as LN is enhanced. Most importantly, this adhesion can be reversed by pre-treating TEC with an anti-alpha 6 integrin mAb. Additionally, spontaneous in vitro thymocyte release by thymic nurse cell complexes was enhanced by LN and partially blocked by anti-alpha 6 or anti-beta 1 antibodies. Our results suggest that VLA6 is involved in LN-mediated TEC-thymocyte interactions that can be relevant for thymic microenvironmental cell physiology and intrathymic T cell differentiation events.
我们在此描述了小鼠胸腺上皮细胞(TEC)中VLA6复合物的表达情况。免疫组织化学分布显示,VLA6在胸腺髓质和被膜下区域均有发现。此外,免疫电子显微镜研究显示VLA6分子存在膜标记,包括在桥粒部位。通过对小鼠TEC系提取物进行免疫印迹、免疫沉淀和亲和层析,我们进一步证明VLA6是这些细胞中的层粘连蛋白(LN)受体。与此发现一致,我们表明LN在体外可增强TEC的黏附、铺展和增殖。VLA6也在大多数胸腺细胞中表达这一事实提出了一个假说,即它可能参与LN介导的TEC与胸腺细胞的相互作用。有趣的是,体外实验表明,糖皮质激素处理后TEC与胸腺细胞的黏附增加,此时VLA6以及LN的表达均增强。最重要的是,用抗α6整合素单克隆抗体预处理TEC可逆转这种黏附。此外,LN可增强胸腺哺育细胞复合物在体外自发释放胸腺细胞的能力,而抗α6或抗β1抗体可部分阻断这种释放。我们的结果表明,VLA6参与LN介导的TEC与胸腺细胞的相互作用,这可能与胸腺微环境细胞生理学和胸腺内T细胞分化事件相关。