Molecular and Cellular Oncogenesis Program, The Wistar Institute, Philadelphia, PA, USA.
Pigment Cell Melanoma Res. 2011 Jun;24(3):422-9. doi: 10.1111/j.1755-148X.2011.00847.x. Epub 2011 Mar 29.
Human multipotent dermal stem cells (DSCs) have been isolated and propagated from the dermal region of neonatal foreskin. DSCs can self-renew, express the neural crest stem cell markers NGFRp75 and nestin, and are capable of differentiating into a wide variety of cell types including mesenchymal and neuronal lineages and melanocytes, indicative of their neural crest origin. When placed in the context of reconstructed skin, DSCs migrate to the basement membrane zone and differentiate into melanocytes. These findings, combined with the identification of NGFRp75-positive cells in the dermis of human foreskin, which are devoid of hair, suggest that DSCs may be a self-renewing source of extrafollicular epidermal melanocytes. In this review, we discuss the properties of DSCs, the pathways required for melanocyte differentiation, and the value of 3D reconstructed skin to assess the behavior and contribution of DSCs in the naturalized environment of human skin. Potentially, DSCs provide a link to malignant melanoma by being a target of UVA-induced transformation.
人多能真皮干细胞(DSC)已从新生儿包皮的真皮区域中分离和增殖。DSC 可以自我更新,表达神经嵴干细胞标志物 NGFRp75 和巢蛋白,并能够分化为多种细胞类型,包括间充质和神经元谱系以及黑素细胞,表明其神经嵴起源。当置于重建皮肤的环境中时,DSC 迁移到基底膜区并分化为黑素细胞。这些发现,加上在没有毛发的人类包皮真皮中鉴定出 NGFRp75 阳性细胞,表明 DSC 可能是毛囊外表皮黑素细胞的自我更新来源。在这篇综述中,我们讨论了 DSC 的特性、黑素细胞分化所需的途径,以及 3D 重建皮肤评估 DSC 在人体皮肤自然环境中的行为和贡献的价值。潜在地,DSC 通过成为 UVA 诱导转化的靶标而与恶性黑色素瘤相关。