Ogaki Soichiro, Omori Hisayoshi, Morooka Mayu, Shiraki Nobuaki, Ishida Seiichi, Kume Shoen
School of Life Science and Technology, Tokyo Institute of Technology, 4259-B-25 Nagatsuta-cho, Midori-ku, Yokohama, Kanagawa, 226-8501, Japan.
Stem Cell Biology, Institute of Molecular Embryology and Genetics, Kumamoto University, Honjo 2-2-1, Kumamoto, 860-0811, Japan.
BMC Dev Biol. 2016 May 31;16(1):19. doi: 10.1186/s12861-016-0120-2.
Definitive endoderm (DE) gives rise to the respiratory apparatus and digestive tract. Sox17 and Cxcr4 are useful markers of the DE. Previously, we identified a novel DE marker, Decay accelerating factor 1(Daf1/CD55), by identifying DE specific genes from the expression profile of DE derived from mouse embryonic stem cells (ESCs) by microarray analysis, and in situ hybridization of early embryos. Daf1 is expressed in a subpopulation of E-cadherin + Cxcr4+ DE cells. The characteristics of the Daf1-expressing cells during DE differentiation has not been examined.
In this report, we utilized the ESC differentiation system to examine the characteristics of Daf1-expressing DE cells. We found that Daf1 expression could discriminate late DE from early DE. Early DE cells are Daf1-negative (DE-) and late DE cells are Daf1-positive (DE+). We also found that Daf1+ late DE cells show low proliferative and low cell matrix adhesive characteristics. Furthermore, the purified SOX17(low) early DE cells gave rise to Daf1+ Sox17(high) late DE cells.
Daf1-expressing late definitive endoderm proliferates slowly and show low adhesive capacity.
确定内胚层(DE)可分化为呼吸器官和消化道。Sox17和Cxcr4是DE的有用标志物。此前,我们通过微阵列分析从小鼠胚胎干细胞(ESC)来源的DE表达谱中鉴定DE特异性基因,并结合早期胚胎的原位杂交,鉴定出一种新的DE标志物,衰变加速因子1(Daf1/CD55)。Daf1在E-钙黏蛋白+ Cxcr4 + DE细胞的一个亚群中表达。尚未研究Daf1表达细胞在DE分化过程中的特征。
在本报告中,我们利用ESC分化系统研究表达Daf1的DE细胞的特征。我们发现Daf1表达可区分早期DE和晚期DE。早期DE细胞为Daf1阴性(DE-),晚期DE细胞为Daf1阳性(DE+)。我们还发现Daf1 +晚期DE细胞具有低增殖和低细胞基质黏附特性。此外,纯化的SOX17(低)早期DE细胞可产生Daf1 + Sox17(高)晚期DE细胞。
表达Daf1的晚期确定内胚层增殖缓慢且黏附能力低。