Hayakawa J, Moriya N, Shiohara T
Department of Dermatology, Kyorin University School of Medicine, Tokyo, Japan.
Cell Immunol. 1996 Dec 15;174(2):190-8. doi: 10.1006/cimm.1996.0309.
It was generally assumed that Vgamma5+ fetal thymocytes are the only cells capable of homing to the epidermis. However, we have recently demonstrated that reconstitution of thymectomized irradiated mice with T-cell-depleted bone marrow (BM) cells results in the appearance of donor-type CD8+, TCR-alphabeta+ dendritic epidermal T cells (DETC) phenotypically distinct from their normal gammadelta+ counterparts. In the present study, we found that the epidermis of lethally irradiated, BM-reconstituted (XBM) mice was also repopulated by DETC of host origin as well as donor BM-derived DETC and that the host-derived DETC were rarely detected in the epidermis of athymic BM chimeras (ATXBM). This result indicates that the host-derived DETC are originated from intrathymic radioresistant cells that may share migratory capacities with the fetal thymocytes. We demonstrated that transfer of radioresistant intrathymic precursor cells into ATXBM mice resulted in the appearance of donor-type CD8+, TCR-alphabeta+ DETC. Contrary to our initial expectation, however, transferred normal adult thymocytes also gave rise to donor-type DETC with frequency similar to radioresistant thymocyte-derived DETC. These thymocyte-derived DETC were phenotypically similar to those derived from BM cells but differed in some respects. Tissue tropism by the CD8+ subset was observed only for the epidermis, but not for other lymphoid organs, such as lymph nodes. The epidermis of normal mice, unlike that of irradiated mice, was refractory to the appearance of the thymus-derived DETC. These results suggest that prior irradiation of the host may confer a susceptibility of the epidermis to repopulation of DETC precursors, which are otherwise incapable of migrating into the epidermis. This provides an explanation for why CD8+, TCR-alphabeta+ DETC of adult thymus or BM origin are rarely detected in the normal epidermis, but abundantly observed in the irradiated mice.
人们普遍认为Vγ5+胎儿胸腺细胞是唯一能够归巢至表皮的细胞。然而,我们最近证明,用去除T细胞的骨髓(BM)细胞重建经胸腺切除和照射的小鼠,会导致出现供体类型的CD8+、TCRαβ+树突状表皮T细胞(DETC),其表型与正常的γδ+对应细胞不同。在本研究中,我们发现,经致死性照射并由BM重建(XBM)的小鼠的表皮,也由宿主来源的DETC以及供体BM来源的DETC重新填充,并且在无胸腺BM嵌合体(ATXBM)的表皮中很少检测到宿主来源的DETC。这一结果表明,宿主来源的DETC起源于胸腺内的抗辐射细胞,这些细胞可能与胎儿胸腺细胞共享迁移能力。我们证明,将抗辐射的胸腺内前体细胞转移到ATXBM小鼠中会导致出现供体类型的CD8+、TCRαβ+ DETC。然而,与我们最初的预期相反,转移的正常成年胸腺细胞也会产生频率与抗辐射胸腺细胞来源的DETC相似的供体类型DETC。这些胸腺细胞来源的DETC在表型上与BM细胞来源的DETC相似,但在某些方面有所不同。仅在表皮中观察到CD8+亚群对组织的嗜性,而在其他淋巴器官如淋巴结中未观察到。与照射小鼠不同,正常小鼠的表皮对胸腺来源的DETC的出现具有抗性。这些结果表明,宿主预先接受照射可能使表皮易受DETC前体的重新填充,否则这些前体无法迁移到表皮中。这就解释了为什么在正常表皮中很少检测到成年胸腺或BM来源的CD8+、TCRαβ+ DETC,但在照射小鼠中却大量观察到。