Zhao Along, Yang Leilei, Ma Kui, Sun Mengli, Li Lei, Huang Jin, Li Yang, Zhang Cuiping, Li Haihong, Fu Xiaobing
a Key Research Laboratory of Tissue Repair and Regeneration of PLA, and Beijing Key Research Laboratory of Skin Injury, Repair and Regeneration, First Hospital Affiliated to the Chinese PLA General Hospital , Beijing , P.R. China.
b Tianjin Medical University , Tianjin , PR China.
Cell Cycle. 2016;15(5):644-53. doi: 10.1080/15384101.2016.1146838.
It has been reported that Wnt/β-catenin is critical for dedifferentiation of differentiated epidermal cells. Cyclin D1 (CCND1) is a β-catenin target gene. In this study, we provide evidence that overexpression of CCND1 induces reprogramming of epidermal cells into stem cell-like cells. After introducing CCND1 gene into differentiated epidermal cells, we found that the large flat-shaped cells with a small nuclear-cytoplasmic ratio changed into small round-shaped cells with a large nuclear-cytoplasmic ratio. The expressions of CK10, β1-integrin, Oct4 and Nanog in CCND1 induced cells were remarkably higher than those in the control group (P < 0.01). In addition, the induced cells exhibited a high colony-forming ability and a long-term proliferative potential. When the induced cells were implanted into a wound of laboratory animal model, the wound healing was accelerated. These results suggested that overexpression of CCND1 induced the reprogramming of differentiated epidermal cells into stem cell-like cells. This study may also offer a new approach to yield epidermal stem cells for wound repair and regeneration.
据报道,Wnt/β-连环蛋白对分化的表皮细胞去分化至关重要。细胞周期蛋白D1(CCND1)是一个β-连环蛋白靶基因。在本研究中,我们提供证据表明CCND1的过表达可诱导表皮细胞重编程为干细胞样细胞。将CCND1基因导入分化的表皮细胞后,我们发现核质比小的大扁平状细胞转变为核质比大的小圆形细胞。CCND1诱导细胞中CK10、β1整合素、Oct4和Nanog的表达明显高于对照组(P<0.01)。此外,诱导细胞表现出高集落形成能力和长期增殖潜力。当将诱导细胞植入实验动物模型的伤口时,伤口愈合加速。这些结果表明CCND1的过表达诱导分化的表皮细胞重编程为干细胞样细胞。本研究也可能为产生用于伤口修复和再生的表皮干细胞提供一种新方法。