Nicolas J F, Auger C, Dardenne M, Thivolet J
Clinique Dermatologique, Inserm U.209, Paris, France.
Thymus. 1988;12(3):187-201.
Cultured human epidermal cells have been shown to produce soluble factors endowed with T cell differentiating activities. In addition, the presence of thymopoietin and FTS/thymulin-like factors has been reported in normal human and mouse epidermis using immunohistochemical methods and anti-thymic hormone antibodies. The present study was conducted to re-evaluate the presence of thymic hormones in normal epidermal cells using a panel of monoclonal antibodies (mAbs) and rabbit antisera to several well characterized thymic factors. The reactivity of the following antibodies was tested by indirect immunofluorescence on human and mouse tissue sections: a) two anti-FTS/thymulin mAbs; b) one anti-FTS/thymulin rabbit antiserum; c) one anti-thymopoietin rabbit antiserum; d) one anti-thymosin alpha 1 mAb. Our results show that: 1) all five antibodies reacted with human and/or mouse thymic epithelial cells; 2) none of the 3 antithymic hormone mAbs (2 anti-FTS/thymulin and 1 anti-thymosin alpha 1 mAbs) reacted with normal skin; 3) only 2 out of 5 antibodies, namely the anti-FTS and anti-thymopoietin antisera cross-reacted with mouse and human epidermis and labeled keratinocytes, as previously reported; these latter 2 antibodies also stained nude mouse epidermal cells and labeled non-thymic, non-epidermal normal mouse epithelial tissues, suggesting that the cross-reactive epitope is common to a number of epithelial cells; 4) the antigen defined by the anti-FTS and anti-thymopoietin antisera was not related to keratins, since absorption experiments using purified human epidermal keratins failed to abolish staining of the epidermis. We conclude from this study that epidermal cells do not produce in vivo the well characterized thymic hormones: FTS/thymulin, thymopoietin and thymosin alpha 1. The precise nature of the antigenic structure recognized within epidermis by the anti-FTS and anti-thymopoietin antibodies remains to be defined.
培养的人表皮细胞已被证明能产生具有T细胞分化活性的可溶性因子。此外,使用免疫组织化学方法和抗胸腺激素抗体,已报道在正常人及小鼠表皮中存在胸腺生成素和FTS/胸腺素样因子。本研究旨在使用一组单克隆抗体(mAb)和针对几种特征明确的胸腺因子的兔抗血清,重新评估正常表皮细胞中胸腺激素的存在情况。通过间接免疫荧光法检测了以下抗体对人和小鼠组织切片的反应性:a)两种抗FTS/胸腺素单克隆抗体;b)一种抗FTS/胸腺素兔抗血清;c)一种抗胸腺生成素兔抗血清;d)一种抗胸腺素α1单克隆抗体。我们的结果表明:1)所有五种抗体均与人及/或小鼠胸腺上皮细胞发生反应;2)三种抗胸腺激素单克隆抗体(两种抗FTS/胸腺素和一种抗胸腺素α1单克隆抗体)均未与正常皮肤发生反应;3)如先前报道,五种抗体中只有两种,即抗FTS和抗胸腺生成素抗血清与小鼠和人表皮发生交叉反应并标记角质形成细胞;这后两种抗体也对裸鼠表皮细胞进行了染色,并标记了非胸腺、非表皮的正常小鼠上皮组织,表明交叉反应表位在许多上皮细胞中是共同的;4)抗FTS和抗胸腺生成素抗血清所定义的抗原与角蛋白无关,因为使用纯化的人表皮角蛋白进行的吸收实验未能消除表皮的染色。我们从这项研究得出结论,表皮细胞在体内不产生特征明确的胸腺激素:FTS/胸腺素、胸腺生成素和胸腺素α1。抗FTS和抗胸腺生成素抗体在表皮中识别的抗原结构的确切性质仍有待确定。