Xie Hongbin, Wang Yunshuai, Zhang Hui, Qi Hui, Zhou Hanxin, Li Fu-Rong
The Key Laboratory of stem cell and cellular therapy, the Second Clinical Medical College (Shenzhen People's Hospital), Jinan University, Shenzhen, China.
PLoS One. 2013 Sep 18;8(9):e76056. doi: 10.1371/journal.pone.0076056. eCollection 2013.
Mesenchymal stem cells (MSCs) can be successfully induced to differentiate into insulin-producing cells (IPCs) by a variety of small molecules and cytokines in vitro. However, problems remain, such as low transdifferentiation efficiency and poor maturity of trans-differentiated cells. The damaged pancreatic cells secreted a large amount of soluble proteins, which were able to promote pancreative islet regeneration and MSCs differentiation. In this study, we utilized the rat injured pancreatic tissue extract to modulate rat bone marrow-derived MSCs differentiation into IPCs by the traditional two-step induction. Our results showed that injured pancreatic tissue extract could effectively promote the trans-differentiation efficiency and maturity of IPCs by the traditional induction. Moreover, IPCs were able to release more insulin in a glucose-dependent manner and ameliorate better the diabetic conditions of streptozotocin (STZ)-treated rats. Our study provides a new strategy to induce an efficient and directional differentiation of MSCs into IPCs.
间充质干细胞(MSCs)在体外可被多种小分子和细胞因子成功诱导分化为胰岛素生成细胞(IPCs)。然而,问题依然存在,比如转分化效率低以及转分化细胞成熟度差。受损的胰腺细胞分泌大量可溶性蛋白,这些蛋白能够促进胰岛再生和间充质干细胞分化。在本研究中,我们利用大鼠损伤胰腺组织提取物,通过传统的两步诱导法来调控大鼠骨髓来源的间充质干细胞分化为胰岛素生成细胞。我们的结果表明,损伤胰腺组织提取物通过传统诱导能够有效提高胰岛素生成细胞的转分化效率和成熟度。此外,胰岛素生成细胞能够以葡萄糖依赖的方式释放更多胰岛素,并更好地改善链脲佐菌素(STZ)处理大鼠的糖尿病状况。我们的研究为诱导间充质干细胞高效定向分化为胰岛素生成细胞提供了一种新策略。