Lin Bojie, Zhu Jiangying, Yin Guoqian, Liao Mingde, Lin Guanyu, Yan Yuyong, Huang Dan, Lu Siding
Department of Plastic and Aesthetic Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Academy of Humanities and Social Sciences, Guangxi Medical University, Nanning, China.
Front Cell Dev Biol. 2021 Jul 15;9:554831. doi: 10.3389/fcell.2021.554831. eCollection 2021.
Adult stem cell function has been one of the most intensively explored areas of biological and biomedical research, with hair follicle stem cells serving as one of the best model systems. This study explored the role of the transcription factor DLX5 in regulating hair follicle stem cell (HFSC) differentiation.
HFSCs were isolated, characterized, and assessed for their expression of DLX5, c-MYC, NSD1, and miR-29c-3p using RT-qPCR, Western blot analysis, or immunofluorescence. Next, the ability of HFSCs to proliferate as well as differentiate into either sebaceous gland cells or epidermal cells was determined. The binding of DLX5 to the c-MYC promoter region, the binding of c-MYC to the miR-29c-3p promoter region, and the binding of miR-29c-3p to the 3'-UTR of NSD1 mRNA were verified by luciferase activity assay and ChIP experiments.
DLX5 was highly expressed in differentiated HFSCs. DLX5 transcriptionally activated c-MYC expression to induce HFSC differentiation. c-MYC was able to bind the miR-29c-3p promoter and thus suppressed its expression. Without miR-29c-3p mediated suppression, NSD1 was then able to promote HFSC differentiation. These experiments suggested that DLX5 could promote HFSC differentiation via the regulation of the c-MYC/miR-29c-3p/NSD1 axis.
This study demonstrates that DLX5 promotes HFSC differentiation by modulating the c-MYC/miR-29c-3p/NSD1 axis and identifies a new mechanism regulating HFSC differentiation.
成体干细胞功能一直是生物学和生物医学研究中探索最为深入的领域之一,毛囊干细胞是其中最佳的模型系统之一。本研究探讨了转录因子DLX5在调节毛囊干细胞(HFSC)分化中的作用。
分离、鉴定HFSC,并通过逆转录定量聚合酶链反应(RT-qPCR)、蛋白质免疫印迹分析或免疫荧光法评估其DLX5、c-MYC、NSD1和miR-29c-3p的表达。接下来,测定HFSC增殖以及分化为皮脂腺细胞或表皮细胞的能力。通过荧光素酶活性测定和染色质免疫沉淀(ChIP)实验验证DLX5与c-MYC启动子区域的结合、c-MYC与miR-29c-3p启动子区域的结合以及miR-29c-3p与NSD1 mRNA的3'-非翻译区(3'-UTR)的结合。
DLX5在分化的HFSC中高表达。DLX5通过转录激活c-MYC表达来诱导HFSC分化。c-MYC能够结合miR-29c-3p启动子,从而抑制其表达。在没有miR-29c-3p介导的抑制作用下,NSD1能够促进HFSC分化。这些实验表明,DLX5可通过调节c-MYC/miR-29c-3p/NSD1轴促进HFSC分化。
本研究表明,DLX5通过调节c-MYC/miR-29c-3p/NSD1轴促进HFSC分化,并确定了一种调节HFSC分化的新机制。