Leibl H, Hutterer J, Korschan H, Schuler G, Tani M, Tschachler E, Romani N, Wolff K, Stingl G
J Invest Dermatol. 1985 Feb;84(2):91-5. doi: 10.1111/1523-1747.ep12274957.
The expression of Ly-5 alloantigens is confined to hemopoietic cell types and is therefore considered a valuable indicator for the bone marrow derivation of a given cell. The further finding that different hemopoietic cell lineages express different molecular forms of the Ly-5 alloantigens prompted us to investigate (1) whether murine epidermal cells or subpopulations thereof express Ly-5 specificities and if so, (2) whether the expression of particular molecular configurations of Ly-5 antigens would allow us to gain a clue about the derivation of certain epidermal cell populations. When epidermal sheets from BALB/c, C57Bl/6, and C3H/He mice, were exposed to monoclonal anti Ly-5.1 antibody in an indirect immunofluorescence technique, a system of evenly distributed, dendritic cells was visualized. Allelic exclusion of the Ly-5 system was demonstrated by replacing anti-Ly-5.1 antibody by anti-Ly-5.2 reagent and by using epidermal sheets from SJL/J mice. Studies on epidermal cell (EC) suspensions revealed that about 1.6-5.2% of C3H/He EC were Ly-5-reactive and that approximately equal numbers of Ly-5-positive cells bore either Thy-1 or Ia antigens. Electron microscopic studies disclosed two morphologically different Ly-5-positive cell populations, i.e., cells of the Langerhans cell lineage and a recently defined cell system, whose most prominent feature is the expression of the Thy-1 antigen. We have termed these cells dendritic Thy-1+EC (dTHY-1+EC). In order to define the molecular configurations of the Ly-5 alloantigens, EC and spleen cells were internally labeled and--after immunoprecipitation of cell-membrane detergent extracts with anti-Ly-5.1--were analyzed on sodium dodecyl sulfate-polyacrylamide gels. Spleen cells yielded 3 bands with a molecular weight of 180,000, 195,000, and 215,000, respectively, as is characteristic for T lymphocytes, non-T/non-B cells, and B lymphocytes. In contrast, a single 195,000-200,000 dalton band was found in precipitates of both untreated and Langerhans cell-depleted (anti-Ia+C) EC. These data demonstrate the existence and active biosynthesis of the Ly-5 alloantigenic system on certain EC populations, i.e., Langerhans cells and dThy-1+EC, and therefore imply that both cell types originate from a bone marrow-derived precursor. The expression of the same molecular configuration of Ly-5 alloantigens on both LC and dThy-1+EC suggest that these two cell populations do not belong either to the T-cell or to the B-cell lineage and imply an ontogenetic relationship between dThy-1+EC and Ia-positive EC.
Ly-5同种异体抗原的表达仅限于造血细胞类型,因此被认为是给定细胞骨髓来源的重要指标。进一步发现不同的造血细胞谱系表达Ly-5同种异体抗原的不同分子形式,促使我们研究:(1)小鼠表皮细胞或其亚群是否表达Ly-5特异性,如果是,(2)Ly-5抗原特定分子构型的表达是否能让我们了解某些表皮细胞群体的来源。当用间接免疫荧光技术将来自BALB/c、C57Bl/6和C3H/He小鼠的表皮片暴露于单克隆抗Ly-5.1抗体时,可观察到一个均匀分布的树突状细胞系统。通过用抗Ly-5.2试剂替代抗Ly-5.1抗体并使用来自SJL/J小鼠的表皮片,证明了Ly-5系统的等位基因排斥。对表皮细胞(EC)悬液的研究表明,约1.6 - 5.2%的C3H/He EC具有Ly-5反应性,且Ly-5阳性细胞中带有Thy-1或Ia抗原的细胞数量大致相等。电子显微镜研究揭示了两种形态不同的Ly-5阳性细胞群体,即朗格汉斯细胞谱系的细胞和一个最近定义的细胞系统,其最显著的特征是Thy-1抗原的表达。我们将这些细胞称为树突状Thy-1 + EC(dTHY-1 + EC)。为了确定Ly-5同种异体抗原的分子构型,对EC和脾细胞进行内标记,并用抗Ly-5.1对细胞膜去污剂提取物进行免疫沉淀后,在十二烷基硫酸钠 - 聚丙烯酰胺凝胶上进行分析。脾细胞产生了分别具有180,000、195,000和215,000分子量的3条带,这是T淋巴细胞、非T/非B细胞和B淋巴细胞的特征。相比之下,在未处理的和去除朗格汉斯细胞(抗Ia + C)的EC沉淀中均发现了一条单一的195,000 - 200,000道尔顿的带。这些数据证明了Ly-5同种异体抗原系统在某些EC群体(即朗格汉斯细胞和dThy-1 + EC)上的存在和活跃生物合成,因此意味着这两种细胞类型均起源于骨髓来源的前体细胞。Ly-5同种异体抗原在LC和dThy-1 + EC上相同分子构型的表达表明,这两个细胞群体既不属于T细胞谱系也不属于B细胞谱系,并暗示了dThy-1 + EC与Ia阳性EC之间的个体发生关系。