β细胞保存和再生用于糖尿病治疗:我们现在在哪里?

Michael J Karadimos, Archana Kapoor, Ilham El Khattabi, Arun Sharma
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引用次数: 3

摘要

在过去的十年中,我们对β细胞生物学的了解随着新的科学技术和策略的使用而扩大。生长因子、激素和小分子已被证明可以增强β细胞的增殖和功能。干细胞技术和对胰腺发育生物学的研究已经为干细胞和内源性祖细胞在体内和体外再生β细胞以及非β细胞的转分化提供了新的方法。新的药理学方法已经开发出来,以保持和增强β细胞的功能。在功能失调和未成熟的β细胞中增加胰岛素基因转录因子表达的策略可以改善这些损伤。因此,我们建议减少β细胞损失并增加其功能和再生的策略将最终导致1型和2型糖尿病的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
β-cell preservation and regeneration for diabetes treatment: where are we now?

Over the last decade, our knowledge of β-cell biology has expanded with the use of new scientific techniques and strategies. Growth factors, hormones and small molecules have been shown to enhance β-cell proliferation and function. Stem cell technology and research into the developmental biology of the pancreas have yielded new methods for in vivo and in vitro regeneration of β cells from stem cells and endogenous progenitors as well as transdifferentiation of non-β cells. Novel pharmacological approaches have been developed to preserve and enhance β-cell function. Strategies to increase expression of insulin gene transcription factors in dysfunctional and immature β cells have ameliorated these impairments. Hence, we suggest that strategies to minimize β-cell loss and to increase their function and regeneration will ultimately lead to therapy for both Type 1 and 2 diabetes.

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