Koga Tomoaki, Shiraki Nobuaki, Yano Shuichiro, Suico Mary Ann, Morino-Koga Saori, Sato Takashi, Shuto Tsuyoshi, Kume Shoen, Kai Hirofumi
Department of Molecular Medicine, Graduate School of Pharmaceutical Sciences, Kumamoto University, 5-1 Oe-honmachi, Chuo-ku, Kumamoto, 862-0973, Japan.
Present address: Department of Biochemistry, Juntendo University School of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo, 113-8421, Japan.
BMC Biotechnol. 2017 Feb 15;17(1):14. doi: 10.1186/s12896-017-0331-z.
Because of the increasing number of diabetic patients, it is important to generate pancreatic and duodenal homeobox gene 1 (Pdx1)-expressing cells, which are capable of differentiating into pancreatic endocrine β cells. Mild electrical stimulation was reported to modulate the differentiation of ES cells into ectoderm-derived neuronal cells or mesoderm-derived cardiac cells.
In this study, we report that mild electrical stimulation with heat shock (MET) potentiates the differentiation of ES cells into definitive endoderm-derived Pdx1-expressing cells. MET has no effect when applied to early definitive endoderm on differentiation day 5. A 1.87-fold increase in the proportion of Pdx1-expressing cells was observed when stimulation was applied to the late definitive endoderm one day prior to the immergence of Pdx1/GFP-expressing cells on differentiation day 7. Pdx1 mRNA was also up-regulated by MET. The potentiating effect of MET synergized with activin and basic fibroblast growth factor into Pdx1-expressing cells. Moreover, MET stimulation on late definitive endoderm up-regulated heat shock protein 72 and activated various kinases including Akt, extracellular signal-regulated kinase, p38, and c-jun NH-terminal kinase in ES cells.
Our findings indicate that MET induces the differentiation of Pdx1-expressing cells within the definitive endoderm in a time-dependent manner, and suggest useful application for regenerative medicine.
由于糖尿病患者数量不断增加,生成能够分化为胰腺内分泌β细胞的胰腺十二指肠同源盒基因1(Pdx1)表达细胞非常重要。据报道,轻度电刺激可调节胚胎干细胞(ES细胞)向外胚层来源的神经细胞或中胚层来源的心脏细胞分化。
在本研究中,我们报告热休克轻度电刺激(MET)可增强ES细胞向定形内胚层来源的Pdx1表达细胞的分化。在分化第5天应用于早期定形内胚层时,MET没有效果。在分化第7天Pdx1/绿色荧光蛋白(GFP)表达细胞出现前一天,当刺激应用于晚期定形内胚层时,观察到Pdx1表达细胞比例增加了1.87倍。MET也上调了Pdx1 mRNA。MET的增强作用与激活素和碱性成纤维细胞生长因子协同作用,促进了Pdx1表达细胞的生成。此外,对晚期定形内胚层的MET刺激上调了热休克蛋白72,并激活了ES细胞中的多种激酶,包括Akt、细胞外信号调节激酶、p38和c-jun氨基末端激酶。
我们的研究结果表明,MET以时间依赖性方式诱导定形内胚层内Pdx1表达细胞的分化,并为再生医学提供了有益的应用。