Bergstresser P R, Tigelaar R E, Streilein J W
J Invest Dermatol. 1984 Aug;83(2):83-7. doi: 10.1111/1523-1747.ep12262587.
Thy-1 antigen is expressed on a dendritic subpopulation of cells in murine epidermis. Numbering between 200 and 500/mm2 surface area in abdominal skin, they are distinct from the dendritic Langerhans cells (LCs) and melanocytes. Since immigrant lymphoid cells as well as constitutive cells in various organs have been demonstrated to be Thy-1+, their origin and function are not certain. To assess these issues, two experimental protocols were established. First, grafts of whole skin from AKR mice were placed orthotopically on (AKD2)F1 recipients. Immigration of recipient-derived cells into graft epidermis was assessed histologically by fluorescence microscopy employing monoclonal anti-Thy-1.2 and anti-I-Ad antibodies. Second, bone marrow chimeras were established in AKR recipients after lethal irradiation and reconstitution with cells from (AKD2)F1 donors. In the first protocol, dendritic I-Ad+ LCs of donor origin infiltrated each graft to normal densities within 2 weeks. Thy-1.2+ cells also immigrated into the same grafts, but at much slower rates. In the second protocol, bone marrow-derived Thy-1.2+ cells populated normal skin epidermis slowly over several months, with densities reaching 70/mm2. We conclude that some, if not all, Thy-1+ cells in normal murine epidermis are derived from bone marrow precursors, that their infiltration rates differ substantially from those of LCs, and that those factors which govern immigration rates into adult skin derive from the skin itself rather than from the systemic availability of their precursors. We suggest that the function of Thy-1+ epidermal cells will therefore reside among those usually ascribed to recirculating hematogenous cells, including the possibility that they may down-regulate immunizing signals that emerge from skin.
Thy-1抗原在小鼠表皮的一个树突状细胞亚群上表达。在腹部皮肤中,每平方毫米表面积有200至500个,它们与树突状朗格汉斯细胞(LCs)和黑素细胞不同。由于已证明各种器官中的移行淋巴细胞以及组成细胞都是Thy-1阳性,它们的起源和功能尚不确定。为了评估这些问题,建立了两个实验方案。首先,将AKR小鼠的全皮移植物原位移植到(AKD2)F1受体上。通过使用单克隆抗Thy-1.2和抗I-Ad抗体的荧光显微镜,从组织学上评估受体来源的细胞向移植物表皮的迁移。其次,在致死性照射并用来自(AKD2)F1供体的细胞重建后,在AKR受体中建立骨髓嵌合体。在第一个方案中,供体来源的树突状I-Ad + LCs在2周内以正常密度浸润每个移植物。Thy-1.2 +细胞也迁移到相同的移植物中,但速度要慢得多。在第二个方案中,骨髓来源的Thy-1.2 +细胞在几个月内缓慢填充正常皮肤表皮,密度达到70/mm2。我们得出结论,正常小鼠表皮中一些(如果不是全部)Thy-1 +细胞源自骨髓前体,它们的浸润率与LCs的浸润率有很大差异,并且那些控制向成年皮肤迁移率的因素来自皮肤本身,而不是其前体的全身可用性。我们建议,Thy-1 +表皮细胞的功能因此将存在于通常归因于循环造血细胞的功能之中,包括它们可能下调从皮肤出现的免疫信号的可能性。