Singer K H, Harden E A, Robertson A L, Lobach D F, Haynes B F
J Invest Dermatol. 1985 Jul;85(1 Suppl):67s-71s. doi: 10.1111/1523-1747.ep12275490.
We have established long term in vitro cultures of human thymic epithelium and human epidermis free of contaminating fibroblasts. The cultured cells were examined using a panel of monoclonal antibodies which were raised against human thymic stroma and recognize tissue specific differentiation antigens of human epidermis and thymic epithelium. A subset of cultured epidermal cells (50%) and thymic epithelial cells (18%) expressed the TE-4 antigen characteristic of basal keratinocytes in skin and endocrine epithelium found in the subcapsular cortex and medulla of the thymus. Subpopulations of the cultured cells expressed the antigens detected by antibodies TE-8 and TE-15. In tissue sections antibodies TE-8 and TE-15 bound to the stratum granulosum and stratum corneum of skin and to the Hassall's bodies of thymus, and therefore recognize antigens characteristic of late stages of keratinized epithelial differentiation. In addition, a subset of thymic epithelial cells expressed the antigen detected by antibody TE-3 which is expressed by nonendocrine thymic epithelium found in the thymic cortex. Thus, in vitro cultures of both epidermal and thymic epithelial cells expressed the entire array of differentiation antigens detected by our panel of monoclonal antibodies. This approach can be used to evaluate the role of components of the thymic microenvironment at various stages of differentiation on developing T lymphocytes. In addition, the cultured epidermal cells can be used to evaluate epidermis as a site of extrathymic T cell maturation.
我们已经建立了无成纤维细胞污染的人胸腺上皮和人表皮的长期体外培养体系。使用一组针对人胸腺基质产生的单克隆抗体对培养的细胞进行检测,这些抗体可识别出人表皮和胸腺上皮的组织特异性分化抗原。一部分培养的表皮细胞(50%)和胸腺上皮细胞(18%)表达了TE-4抗原,该抗原是皮肤基底角质形成细胞以及胸腺被膜下皮质和髓质中内分泌上皮的特征性抗原。培养细胞的亚群表达了由抗体TE-8和TE-15检测到的抗原。在组织切片中,抗体TE-8和TE-15与皮肤的颗粒层和角质层以及胸腺的哈氏小体结合,因此识别角质化上皮分化后期的特征性抗原。此外,一部分胸腺上皮细胞表达了由抗体TE-3检测到的抗原,该抗原由胸腺皮质中非内分泌性胸腺上皮表达。因此,表皮和胸腺上皮细胞的体外培养物表达了我们这组单克隆抗体所检测到的全部系列的分化抗原。这种方法可用于评估胸腺微环境成分在发育中的T淋巴细胞分化的各个阶段所起的作用。此外,培养的表皮细胞可用于评估表皮作为胸腺外T细胞成熟部位的情况。