Martinez-Gamboa Marisela, Cruz-Vega Delia Elba, Moreno-Cuevas Jorge, Gonzalez-Garza Maria Teresa
Escuela De Ciencias De La Salud, Valle de las Palmas, Universidad Autónoma de Baja California, Tijuana, B.C, CP 22263, México.
Cell Therapy Group, Escuela Nacional De Medicina, Tecnológico de Monterrey, Monterrey, CP 64710, NL, México.
Int J Stem Cells. 2017 May 30;10(1):76-82. doi: 10.15283/ijsc16040.
Diabetes constitutes a worldwide epidemic that affects all ethnic groups. Cell therapy is one of the best alternatives of treatment, by providing an effective way to regenerate insulin-producing cells lost during the course of the disease, but many issues remain to be solved. Several groups have been working in the development of a protocol capable of differentiating Mesenchymal Stem Cells (MSCs) into physiologically sound Insulin Producing Cells (IPCs). In order to obtain a simple, fast and direct method, we propose in this manuscript the induction of MSCs to express NESTIN in a short time period (2 h), proceeded by incubation in a low glucose induced medium (24 h) and lastly by incubation in a high glucose medium. Samples from cell cultures incubated in high glucose medium from 12 to 168 h were obtained to detect the expression of INSULIN-1, INSULIN -2, PDX-1 and GLUT-2 genes. Induced cells were exposed to a glucose challenge, in order to assess the production of insulin. This method allowed us to obtain cells expressing PDX-1, which resembles a progenitor insulin-producing cell.
糖尿病是一种影响所有种族群体的全球性流行病。细胞疗法是最佳治疗选择之一,它为再生疾病过程中丢失的胰岛素产生细胞提供了有效途径,但仍有许多问题有待解决。几个研究团队一直致力于开发一种方案,能够将间充质干细胞(MSC)分化为生理功能健全的胰岛素产生细胞(IPC)。为了获得一种简单、快速且直接的方法,我们在本论文中提出,先在短时间内(2小时)诱导MSC表达巢蛋白(NESTIN),接着在低葡萄糖诱导培养基中孵育(24小时),最后在高葡萄糖培养基中孵育。获取在高葡萄糖培养基中孵育12至168小时的细胞培养样本,以检测胰岛素-1、胰岛素-2、胰腺十二指肠同源盒-1(PDX-1)和葡萄糖转运蛋白-2(GLUT-2)基因的表达。将诱导后的细胞进行葡萄糖刺激试验,以评估胰岛素的产生情况。该方法使我们能够获得表达PDX-1的细胞,这类细胞类似于胰岛素产生祖细胞。