Department of Genetics, Stanford University, Stanford, Calif.
Department of Medicine, Stanford University Medical School, Stanford, Calif.
Transl Res. 2014 Apr;163(4):418-31. doi: 10.1016/j.trsl.2013.11.012. Epub 2013 Nov 27.
The diabetes pandemic incurs extraordinary public health and financial costs that are projected to expand for the foreseeable future. Consequently, the development of definitive therapies for diabetes is a priority. Currently, a wide spectrum of therapeutic strategies-from implantable insulin delivery devices to transplantation-based cell replacement therapy, to β-cell regeneration-focus on replacing the lost insulin-producing capacity of individuals with diabetes. Among these, β-cell regeneration remains promising but heretofore unproved. Indeed, recent experimental work has uncovered surprising biology that underscores the potential therapeutic benefit of β-cell regeneration. These studies have elucidated a variety of sources for the endogenous production of new β cells from existing cells. First, β cells, long thought to be postmitotic, have demonstrated the potential for regenerative capacity. Second, the presence of pancreatic facultative endocrine progenitor cells has been established. Third, the malleability of cellular identity has availed the possibility of generating β cells from other differentiated cell types. Here, we review the exciting developments surrounding endogenous sources of β-cell production and consider the potential of realizing a regenerative therapy for diabetes from adult tissues.
糖尿病的流行给公共卫生和财政带来了巨大的负担,预计在可预见的未来还会继续扩大。因此,开发糖尿病的明确治疗方法是当务之急。目前,从可植入胰岛素输送装置到基于移植的细胞替代疗法,再到β细胞再生,各种治疗策略都聚焦于取代糖尿病患者丧失的胰岛素产生能力。在这些方法中,β细胞再生仍然很有前途,但尚未得到证实。事实上,最近的实验工作揭示了令人惊讶的生物学现象,强调了β细胞再生的潜在治疗益处。这些研究阐明了多种内源性产生新β细胞的来源,从现有的细胞中产生新的β细胞。首先,β细胞长期以来被认为是有丝分裂后细胞,但现在已经证明它们具有再生能力。其次,已经确定了胰腺兼性内分泌祖细胞的存在。第三,细胞身份的可变性为从其他分化细胞类型生成β细胞提供了可能性。在这里,我们回顾了围绕β细胞产生的内源性来源的令人兴奋的发展,并考虑了从成人组织中实现糖尿病再生治疗的潜力。