State Key Laboratory of Natural and Biomimetic Drugs, Department of Chemical Biology, Peking University School of Pharmaceutical Sciences, Beijing, 100191, China.
Department of Stem Cell and Regenerative Biology, Harvard Stem Cell Institute, Harvard University, Cambridge, 02138, USA.
Sci China Life Sci. 2017 Mar;60(3):239-248. doi: 10.1007/s11427-016-0211-3. Epub 2016 Oct 27.
Around 400 million people worldwide suffer from diabetes mellitus. The major pathological event for Type 1 diabetes and advanced Type 2 diabetes is loss or impairment of insulin-secreting β cells of the pancreas. For the past 100 years, daily insulin injection has served as a life-saving treatment for these patients. However, insulin injection often cannot achieve full glucose control, and over time poor glucose control leads to severe complications and mortality. As an alternative treatment, islet transplantation has been demonstrated to effectively maintain glucose homeostasis in diabetic patients, but its wide application is limited by the scarcity of donated islets. Therefore, it is important to define new strategies to obtain functional human β cells for transplantation therapies. Here, we summarize recent progress towards the production of β cells in vitro from pluripotent stem cells or somatic cell types including α cells, pancreatic exocrine cells, gastrointestinal stem cells, fibroblasts and hepatocytes. We also discuss novel methods for optimizing β cell transplantation and maintenance in vivo. From our perspective, the future of β cell replacement therapy is very promising although it is still challenging to control differentiation of β cells in vitro and to protect these cells from autoimmune attack in Type 1 diabetic patients. Overall, tremendous progress has been made in understanding β cell differentiation and producing functional β cells with different methods. In the coming years, we believe more clinical trials will be launched to move these technologies towards treatments to benefit diabetic patients.
全球约有 4 亿人患有糖尿病。1 型糖尿病和晚期 2 型糖尿病的主要病理事件是胰腺胰岛素分泌β细胞的丧失或损伤。在过去的 100 年中,每天注射胰岛素一直是这些患者的救命治疗方法。然而,胰岛素注射往往无法实现完全的血糖控制,随着时间的推移,血糖控制不佳会导致严重的并发症和死亡率。作为替代治疗方法,胰岛移植已被证明可有效维持糖尿病患者的葡萄糖稳态,但由于供体胰岛的稀缺,其广泛应用受到限制。因此,确定获得用于移植治疗的功能性人β细胞的新策略非常重要。在这里,我们总结了最近在从多能干细胞或体细胞类型(包括α细胞、胰腺外分泌细胞、胃肠道干细胞、成纤维细胞和肝细胞)体外产生β细胞方面的进展。我们还讨论了优化体内β细胞移植和维持的新方法。从我们的角度来看,尽管在体外控制β细胞分化和保护 1 型糖尿病患者自身免疫攻击方面仍具有挑战性,但β细胞替代治疗的未来非常有希望。总的来说,在理解β细胞分化和使用不同方法产生功能性β细胞方面已经取得了巨大的进展。在未来几年,我们相信将开展更多的临床试验,将这些技术推向造福糖尿病患者的治疗方法。