Department of Human Molecular Genetics and Biochemistry, Sackler School of Medicine, Tel Aviv University, Ramat Aviv, Tel Aviv, Israel.
Diabetes Obes Metab. 2016 Sep;18 Suppl 1:97-101. doi: 10.1111/dom.12724.
Recent studies in animal models and human pathological specimens suggest the involvement of β-cell dedifferentiation in β-cell dysfunction associated with type 2 diabetes. Dedifferentiated β-cells may be exploited for endogenous renewal of the β-cell mass. However, studying human β-cell dedifferentiation in diabetes presents major difficulties. We have analysed mechanisms involved in human β-cell dedifferentiation in vitro, under conditions that allow cell proliferation. Although there are important differences between the two cellular environments, β-cell dedifferentiation in the two conditions is likely to share a number of common pathways. Insights from the in vitro studies may lead to development of approaches for redifferentiation of endogenous dedifferentiated β-cells.
最近在动物模型和人类病理标本中的研究表明,β 细胞去分化与 2 型糖尿病相关的β 细胞功能障碍有关。去分化的β 细胞可能被用于内源性β 细胞质量的更新。然而,在糖尿病中研究人类β 细胞去分化存在很大的困难。我们已经分析了在允许细胞增殖的体外条件下人类β 细胞去分化所涉及的机制。尽管两种细胞环境之间存在重要差异,但两种条件下的β 细胞去分化可能具有一些共同的途径。体外研究的结果可能会导致开发内源性去分化的β 细胞再分化的方法。