Department of Neuroscience and Cell Biology, UMDNJ-Robert Wood Johnson Medical School, Piscataway, New Jersey, USA.
Dev Neurobiol. 2012 Jun;72(6):821-42. doi: 10.1002/dneu.20999.
The members of the CIP/KIP family of cyclin-dependent kinase (CDK) inhibitory proteins (CKIs), including p57(KIP2), p27(KIP1), and p21(CIP1), block the progression of the cell cycle by binding and inhibiting cyclin/CDK complexes of the G1 phase. In addition to this well-characterized function, p57(KIP2) and p27(KIP1) have been shown to participate in an increasing number of other important cellular processes including cell fate and differentiation, cell motility and migration, and cell death/survival, both in peripheral and central nervous systems. Increasing evidence over the past few years has characterized the functions of the newest CIP/KIP member p57(KIP2) in orchestrating cell proliferation, differentiation, and migration during neurogenesis. Here, we focus our discussion on the multiple roles played by p57(KIP2) during cortical development, making comparisons to p27(KIP1) as well as the INK4 family of CKIs.
CIP/KIP 家族的细胞周期蛋白依赖性激酶 (CDK) 抑制蛋白 (CKIs) 成员,包括 p57(KIP2)、p27(KIP1) 和 p21(CIP1),通过与 G1 期的细胞周期蛋白/CDK 复合物结合并抑制其活性来阻止细胞周期的进程。除了这个特征明确的功能外,p57(KIP2)和 p27(KIP1)还被证明参与了越来越多的其他重要细胞过程,包括外周和中枢神经系统中的细胞命运和分化、细胞运动和迁移以及细胞死亡/存活。过去几年的大量证据描述了最新的 CIP/KIP 成员 p57(KIP2)在神经发生过程中协调细胞增殖、分化和迁移的功能。在这里,我们重点讨论 p57(KIP2)在皮质发育过程中发挥的多种作用,并与 p27(KIP1)以及 INK4 家族的 CKIs 进行比较。