Zhong Wa, Lai Yu, Yu Tao, Xia Zhong Sheng, Yuan Yu Hong, Ouyang Hui, Shan Ti Dong, Chen Qi Kui
Department of Gastroenterology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Yuexiu District, Guangzhou, Guangdong, People Republic of China;
Rom J Morphol Embryol. 2017;58(2):527-535.
Induced differentiation of definitive endoderm (DE) from embryonic stem cells (ESCs) has been the recent focus of studies investigating regeneration and transplantation of organs of the digestive system. Poor cell survival is the most important challenge to DE differentiation from ESCs. This study aimed to optimize culture conditions to promote the differentiation of mouse ESCs into DE, and to investigate the roles of the Wnt and Nodal signaling pathways in the DE differentiation. The mouse ESCs were treated with or without leukemia inhibitory factor, Wnt3a and Activin A alone or together, and examined the DE differentiation by the DE marker CXCR4 and the ESC marker Oct4. The result showed the optimal induction of differentiation was achieved in cells simultaneously treated with Wnt3a and Activin A. Induction of CXCR4 was also earlier when there was simultaneous activation of Wnt and Nodal signaling compared to the groups treated with only Wnt3a or Activin A alone. These findings provide the basis for the induced differentiation of ESCs for the generation of functional, mature cells of gastrointestinal lineage, which can be potentially used for cell replacement therapy, disease modeling, as well as drug discovery studies.
从胚胎干细胞(ESC)诱导分化出确定内胚层(DE)一直是近期研究消化系统器官再生和移植的重点。细胞存活率低是ESC向DE分化面临的最重要挑战。本研究旨在优化培养条件以促进小鼠ESC向DE分化,并研究Wnt和Nodal信号通路在DE分化中的作用。将小鼠ESC单独或联合用或不用白血病抑制因子、Wnt3a和激活素A处理,并用DE标记物CXCR4和ESC标记物Oct4检测DE分化情况。结果显示,在用Wnt3a和激活素A同时处理的细胞中实现了最佳诱导分化。与仅用Wnt3a或激活素A单独处理的组相比,当Wnt和Nodal信号同时激活时,CXCR4的诱导也更早。这些发现为ESC诱导分化生成功能性、成熟的胃肠道谱系细胞提供了基础,这些细胞可潜在地用于细胞替代治疗、疾病建模以及药物发现研究。