Niderla-Bielinska Justyna, Jankowska-Steifer Ewa, Moskalewski Stanislaw
Department of Histology and Embryology, Medical University of Warsaw, Chalubinskiego 5, 02-004 Warsaw, Poland.
Arch Dermatol Res. 2009 Jun;301(5):337-45. doi: 10.1007/s00403-008-0876-8. Epub 2008 Jul 22.
The purpose of the present study was to elucidate why keratinocytes of the outer root sheath (ORS) do not keratinize in situ. Two possibilities were considered--inhibition of keratinization is caused by contact of ORS with inner root sheath (IRS) or insufficient supply of keratinization promoting factors from the surrounding tissues to the ORS. In order to distinguish between these possibilities mid-segments of hair follicles were liberated from the dermis by dissection followed by collagenase digestion. ORS cells were then either allowed to migrate from the mid-segments or were kept on the agarose layer which prevented cell spreading and preserved three dimensional structure of hair root. Cultures were stimulated with calcium or EGF, and studied morphologically at the light and transmission electron microscope level. The level of mRNA for differentiation cell markers was also studied by RealTime PCR. ORS cells growing in a medium with low Ca2+ content formed monolayers, which after elevation of Ca2+ produced multilayers with cells containing keratohyalin-like granules. Ca2+ or EGF treatment upregulated expression of involucrin, filaggrin and keratinocyte differentiation associated protein (Kdap). Culture of mid-segments of hair follicles in low calcium culture medium kept on agarose increased expression of filaggrin and Kdap, but downregulated expression of involucrin. Stimulation by Ca2+ further increased expression of filaggrin and Kdap, but had no effect on the level of involucrin expression. EGF stimulated expression of filaggrin only. It is concluded that IRS exerted an inhibitory effect on the expression of involucrin, an essential component of the cornified envelope, thus preventing keratinization of ORS cells in situ. On the other hand, improved access of nutrients or promoting factors of keratinization to the mid-segment of hair follicles augmented expression of filaggrin and Kdap, proteins engaged in the differentiation of keratinocytes but not involved in its terminal phase.
本研究的目的是阐明外根鞘(ORS)的角质形成细胞为何不在原位发生角质化。考虑了两种可能性——角质化的抑制是由ORS与内根鞘(IRS)接触引起的,或者是周围组织向ORS供应的角质化促进因子不足。为了区分这些可能性,通过解剖从真皮中分离出毛囊中段,随后进行胶原酶消化。然后,让ORS细胞从毛囊中段迁移,或者将其置于琼脂糖层上,该琼脂糖层可防止细胞铺展并保留毛根的三维结构。用钙或表皮生长因子(EGF)刺激培养物,并在光学显微镜和透射电子显微镜水平进行形态学研究。还通过实时聚合酶链反应(RealTime PCR)研究了分化细胞标志物的mRNA水平。在低钙含量培养基中生长的ORS细胞形成单层,在钙浓度升高后形成多层,其中的细胞含有透明角质颗粒样颗粒。钙或EGF处理上调了内披蛋白、丝聚合蛋白和角质形成细胞分化相关蛋白(Kdap)的表达。在琼脂糖上的低钙培养基中培养毛囊中段可增加丝聚合蛋白和Kdap的表达,但下调内披蛋白的表达。钙刺激进一步增加了丝聚合蛋白和Kdap的表达,但对内披蛋白的表达水平没有影响。EGF仅刺激丝聚合蛋白的表达。得出的结论是,IRS对角质化包膜的重要成分内披蛋白的表达产生抑制作用,从而阻止ORS细胞在原位发生角质化。另一方面,改善毛囊中段获取营养物质或角质化促进因子的情况可增强丝聚合蛋白和Kdap的表达,这两种蛋白参与角质形成细胞的分化但不参与其终末阶段。