Kawai K, Suzuki H, Tomiyama K, Minagawa M, Mak T W, Ohashi P S
Department of Dermatology, Niigata University School of Medicine, Japan.
J Invest Dermatol. 1998 Jun;110(6):961-5. doi: 10.1046/j.1523-1747.1998.00214.x.
Vgamma3 TCR cells develop in the fetal thymus and migrate to the skin as dendritic epidermal T cells (DETC). Fetal Vgamma3 thymocytes differentiate from immature heat stable antigen (HSA)high cells to mature HSAlow cells and the latter subset predominantly expresses IL-2 receptor beta chain (IL-2Rbeta). In this study, the role of IL-2Rbeta in the development of Vgamma3 cells was determined in IL-2Rbeta-deficient mice. There was a moderate reduction of mature HSAlow Vgamma3 thymocytes in IL-2Rbeta-deficient mice. Small numbers of Vgamma3 DETC were detected in the fetal skin of IL-2Rbeta-deficient mice, but they were absent in newborn and adult mice. These results suggest that IL-2Rbeta may transduce the crucial signal for survival and/or expansion of Vgama3 cells in the fetal thymus and in the fetal skin. In normal mice, IL-15 but not IL-2 mRNA was expressed in the fetal epidermis and exogenous addition of low concentration of IL-15 to fetal skin organ culture induced proliferation of Vgamma3 DETC. The dependence of fetal Vgamma3 DETC on the expression of IL-2Rbeta and the presence of IL-15 mRNA in the fetal epidermis imply an essential role of IL-15 signaling through IL-2Rbeta in the selective localization of this gammadelta T cell subpopulation in the skin.
Vγ3 TCR细胞在胎儿胸腺中发育,并作为树突状表皮T细胞(DETC)迁移至皮肤。胎儿Vγ3胸腺细胞从不成熟的高耐热抗原(HSA)细胞分化为成熟的低HSA细胞,后一亚群主要表达白细胞介素-2受体β链(IL-2Rβ)。在本研究中,在IL-2Rβ缺陷小鼠中确定了IL-2Rβ在Vγ3细胞发育中的作用。IL-2Rβ缺陷小鼠中成熟的低HSA Vγ3胸腺细胞有适度减少。在IL-2Rβ缺陷小鼠的胎儿皮肤中检测到少量Vγ3 DETC,但在新生和成年小鼠中不存在。这些结果表明,IL-2Rβ可能转导胎儿胸腺和胎儿皮肤中Vγ3细胞存活和/或扩增的关键信号。在正常小鼠中,胎儿表皮中表达IL-15而非IL-2 mRNA,向胎儿皮肤器官培养物中外源添加低浓度IL-15可诱导Vγ3 DETC增殖。胎儿Vγ3 DETC对IL-2Rβ表达的依赖性以及胎儿表皮中IL-15 mRNA的存在意味着IL-15通过IL-2Rβ信号在该γδ T细胞亚群在皮肤中的选择性定位中起重要作用。