Li Li, Lili Ren, Hui Qi, Min Wang, Xue Wen, Xin Shen, Jing Liu, Yan Li, Yeqiang Liu, Fenrong He, Furong Li, Guanxin Shen
Department of Immunology, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
Tissue Cell. 2008 Dec;40(6):437-45. doi: 10.1016/j.tice.2008.04.006. Epub 2008 Jun 24.
We identified that nestin-EGFP-positive cells isolated by fluorescent-activated cell sorting (FACS) were downstream progenitor cells from colony-initiating pancreatic precursor cells. Under differentiation condition, these nestin-EGFP-positive cells could generate islet and neural cells. To investigate the conditions that allowed nestin-EGFP-positive progenitor cells (NPPCs) to efficaciously differentiate into insulin-producing cells in vitro, protocols were designed with glucagon-like peptide-1 (GLP-1) and the histone deacetylase inhibitor, sodium butyrate. We demonstrated that the combination of GLP-1 and sodium butyrate resulted in the increasing of levels of transcripts encoding pancreatic developmental factors and insulin. As a consequence, the amount of insulin-producing cells and insulin secretion were enhanced. These results indicated that NPPCs which were cultured in the presence of GLP-1 and sodium butyrate could specially differentiate into insulin-producing cells.
我们确定,通过荧光激活细胞分选(FACS)分离出的巢蛋白-增强绿色荧光蛋白(nestin-EGFP)阳性细胞是集落起始胰腺前体细胞的下游祖细胞。在分化条件下,这些巢蛋白-EGFP阳性细胞可生成胰岛细胞和神经细胞。为了研究使巢蛋白-EGFP阳性祖细胞(NPPCs)在体外有效分化为胰岛素分泌细胞的条件,设计了使用胰高血糖素样肽-1(GLP-1)和组蛋白去乙酰化酶抑制剂丁酸钠的方案。我们证明,GLP-1和丁酸钠的组合导致编码胰腺发育因子和胰岛素的转录本水平增加。结果,胰岛素分泌细胞的数量和胰岛素分泌增加。这些结果表明,在GLP-1和丁酸钠存在下培养的NPPCs可特异性分化为胰岛素分泌细胞。