Rane S G, Reddy E P
Fels Institute For Cancer Research And Molecular Biology, Temple University, School Of Medicine, 3307 North Broad Street. Philadelphia, PA 19140, USA.
Front Biosci. 2000 Jan 1;5:D1-19. doi: 10.2741/rane.
Diabetes mellitus ensues as a consequence of the body's inability to respond normally to high blood glucose levels. The onset of diabetes is due to several pathological changes, which are a reflection of either the inability of the pancreatic beta cells to secrete sufficient insulin to combat the hyperglycemia or a state of insulin resistance in target tissues. However, the significance of changes in beta cell mass and decreased beta cell proliferation or growth in progression of diabetes has been under-appreciated. Beta cells, like all other cells of our body are under the regulatory checks and balances enforced by changes in cell cycle progression. However, very little is known regarding the key components of the cell cycle machinery regulating cell cycle control of beta cells. Knowledge of key elements involved in cell cycle regulation of beta cells will go a long way in improving our understanding of the replication capacity and developmental biology of beta cells. This information is essential for us to design new approaches that can be used to correct beta cell deficiency in diabetes. This review focuses on the current knowledge of factors important for proliferation of beta cells and proposes a cell cycle model for regeneration of the beta cell population lost or reduced in diabetes.
糖尿病是由于身体无法对高血糖水平做出正常反应而引发的。糖尿病的发病是由多种病理变化所致,这些变化反映出要么胰腺β细胞无法分泌足够的胰岛素来对抗高血糖,要么是靶组织存在胰岛素抵抗状态。然而,β细胞数量的变化以及β细胞增殖或生长减少在糖尿病进展中的重要性一直未得到充分重视。β细胞与我们身体的所有其他细胞一样,受到细胞周期进程变化所实施的调节制衡。然而,对于调节β细胞周期控制的细胞周期机制的关键组成部分,我们所知甚少。了解参与β细胞周期调节的关键因素,将大大有助于我们增进对β细胞复制能力和发育生物学的理解。这些信息对于我们设计可用于纠正糖尿病中β细胞缺陷的新方法至关重要。本综述聚焦于目前对β细胞增殖重要因素的认识,并提出一个细胞周期模型,用于再生在糖尿病中丢失或减少的β细胞群体。