Pioneer Valley Life Science Institute, University of Massachusetts Amherst, Springfield, MA 01107, USA.
Trends Endocrinol Metab. 2010 Jul;21(7):441-8. doi: 10.1016/j.tem.2010.02.008. Epub 2010 Apr 8.
Loss of functional beta-cells is the primary cause of type 2 diabetes, so that there is an acute need to understand how beta-cell number and function are regulated in the adult under normal physiological conditions. Recent studies suggest that members of the transforming growth factor (TGF)-beta family regulate beta-cell function and glucose homeostasis. These factors are also likely to influence beta-cell proliferation and/or the incorporation of new beta-cells from progenitors in adults. Soluble TGFbeta antagonists also appear to have important roles in maintaining homeostasis, and the coordinated activity of TGFbeta family members is likely to regulate the differentiation and function of adult beta-cells, raising the possibility of developing new diabetes therapies based on TGFbeta agonists or antagonists.
功能性β细胞的丧失是 2 型糖尿病的主要病因,因此迫切需要了解在正常生理条件下,β细胞数量和功能是如何受到调节的。最近的研究表明,转化生长因子 (TGF)-β家族的成员调节β细胞功能和葡萄糖稳态。这些因子也可能影响成年个体中β细胞的增殖和/或祖细胞的新β细胞的掺入。可溶性 TGFβ拮抗剂似乎在维持内稳态方面也起着重要作用,TGFβ家族成员的协调活动可能调节成年β细胞的分化和功能,这为基于 TGFβ激动剂或拮抗剂开发新的糖尿病治疗方法提供了可能性。