Yang J S, Lavker R M, Sun T T
Ronald O. Perelman Department of Dermatology, Kaplan Comprehensive Cancer Center, New York University Medical School, New York 10016.
J Invest Dermatol. 1993 Nov;101(5):652-9. doi: 10.1111/1523-1747.ep12371671.
We and others have shown previously that corneal keratinocyte stem cells can proliferate in vitro better than their progeny cells. In this paper, we applied this approach to the identification of hair follicular stem cells. When human scalp hair follicles were placed in explant culture, the bulge area yielded best outgrowths. In another experiment, we isolated different subpopulations of human follicular keratinocytes by micro-dissection, dispersed them by trypsin/EDTA into single cells, and grew them in the presence of 3T3 feeder cells. The keratinocytes were then subcultured under identical conditions to compare their in vitro life span. Our results indicate that the life span of keratinocytes of the upper follicle (containing mainly the isthmus area) > sebaceous gland > lower follicle (between the bulge and bulb) > bulb (containing the matrix cells). The cultured upper follicular keratinocytes tend to be small and relatively uniform in size. The poor in vitro growth of matrix cells may reflect their non-stem cell nature and/or special growth requirement(s) satisfied in vivo by the neighboring dermal papilla cells. Unexpectedly, we found that the upper follicular keratinocytes grow even better than epidermal keratinocytes. The existence of a subpopulation of keratinocytes with an in vitro growth potential superior than other known keratinocytes of the skin supports the hypothesis that follicular stem cells reside in the upper follicle. Our data also raise the possibility that putative follicular stem cells are involved not only in forming the follicle, but also in the long-term maintenance of the epidermis. Finally, we discuss the possibility that keratinocyte stem cells, as defined by their in vivo slow-cycling nature, are absent in culture.
我们和其他研究人员之前已经表明,角膜角质形成干细胞在体外的增殖能力优于其子代细胞。在本文中,我们将这种方法应用于毛囊干细胞的鉴定。当将人类头皮毛囊置于外植体培养时,隆突区域产生的生长效果最佳。在另一项实验中,我们通过显微切割分离出人类毛囊角质形成细胞的不同亚群,用胰蛋白酶/乙二胺四乙酸将它们分散成单个细胞,并在3T3饲养细胞存在的情况下进行培养。然后在相同条件下对角质形成细胞进行传代培养,以比较它们在体外的寿命。我们的结果表明,毛囊上部(主要包含峡部区域)的角质形成细胞寿命>皮脂腺>毛囊下部(在隆突和毛囊球之间)>毛囊球(包含基质细胞)。培养的毛囊上部角质形成细胞往往较小且大小相对均匀。基质细胞在体外生长不佳可能反映了它们的非干细胞性质和/或在体内由相邻真皮乳头细胞满足的特殊生长需求。出乎意料的是,我们发现毛囊上部角质形成细胞的生长甚至比表皮角质形成细胞更好。存在一个体外生长潜力优于皮肤其他已知角质形成细胞的角质形成细胞亚群,这支持了毛囊干细胞存在于毛囊上部的假说。我们的数据还提出了一种可能性,即假定的毛囊干细胞不仅参与毛囊的形成,还参与表皮的长期维持。最后,我们讨论了在培养物中不存在根据其体内慢循环性质定义的角质形成干细胞的可能性。