Zheng Hanxue, Li Linfeng, Wang Du, Zhang Shengchao, Li Wenhui, Cheng Mengdi, Ge Cui, Chen Jiayi, Qiang Yanmei, Chen Fulin, Yu Yuan
Laboratory of Tissue Engineering, College of Life Sciences, Northwest University, Xi'an, China.
Laboratory of Tissue Engineering, College of Life Sciences, Northwest University, Xi'an, China; Provincial Key Laboratory of Biotechnology of Shaanxi, Northwest University, Xi'an, China; Key Laboratory of Resource Biology and Biotechnology in Western China, Ministry of Education, School of Medicine, Northwest University, Xi'an, China.
Int J Biol Macromol. 2025 Feb;288:138729. doi: 10.1016/j.ijbiomac.2024.138729. Epub 2024 Dec 12.
Stem cells are of great importance in the maintenance and regeneration of tissues, with Forkhead box O (FoxO) proteins emerging as pivotal regulators of their functions. However, the precise impact of FoxO proteins on stem cell behavior within regenerative environments remains ambiguous. Planarians, renowned for their abundance of adult stem cells (neoblasts), serve as an excellent model for investigating the dynamics of stem cells during regeneration. In this study, we identified DjfoxO, a conserved foxO gene in the planarian Dugesia japonica, and demonstrated its expression in neoblasts, with elevated levels detected in the regenerative blastema during the regeneration process. Using a FoxO inhibitor (AS1842856) together with RNA interference techniques, we demonstrated that inhibition of FoxO signaling in planarians hinders the regeneration of missing tissues, including the central nervous system, eyespots, anterior intestinal branches, and pharynx. It is noteworthy that the knockdown of DjfoxO does not significantly affect the mitotic activity of neoblasts. Conversely, it impedes the production of lineage-specific progenitors, potentially via modulation of the Erk pathway. These findings elucidate the instructive function of FoxO signaling in regulating stem cell differentiation and provide valuable insights into its potential for improving stem cell-based regenerative therapies.
干细胞在组织的维持和再生中至关重要,叉头框O(FoxO)蛋白已成为其功能的关键调节因子。然而,FoxO蛋白在再生环境中对干细胞行为的确切影响仍不明确。涡虫以其丰富的成体干细胞(新细胞)而闻名,是研究再生过程中干细胞动态的优秀模型。在本研究中,我们鉴定了日本三角涡虫中一个保守的foxO基因DjfoxO,并证明其在新细胞中表达,在再生过程中再生芽基中检测到其水平升高。使用FoxO抑制剂(AS1842856)和RNA干扰技术,我们证明抑制涡虫中的FoxO信号会阻碍缺失组织的再生,包括中枢神经系统、眼点、前肠分支和咽。值得注意的是,DjfoxO的敲低不会显著影响新细胞的有丝分裂活性。相反,它可能通过调节Erk途径阻碍谱系特异性祖细胞的产生。这些发现阐明了FoxO信号在调节干细胞分化中的指导功能,并为其改善基于干细胞的再生疗法的潜力提供了有价值的见解。