Joseph Bertrand, Wallén-Mackenzie Asa, Benoit Gérard, Murata Takashi, Joodmardi Eliza, Okret Sam, Perlmann Thomas
The Ludwig Institute for Cancer Research, Box 240, S-171 77 Stockholm, Sweden.
Proc Natl Acad Sci U S A. 2003 Dec 23;100(26):15619-24. doi: 10.1073/pnas.2635658100. Epub 2003 Dec 11.
Cyclin-dependent kinase inhibitors of the Cip/Kip family play critical roles in regulating cell proliferation during embryogenesis. However, these proteins also influence cell differentiation by mechanisms that have remained unknown. Here we show that p57Kip2 is expressed in postmitotic differentiating midbrain dopamine cells. Induction of p57Kip2 expression depends on Nurr1, an orphan nuclear receptor that is essential for dopamine neuron development. Moreover, analyses of p57Kip2 gene-targeted mice revealed that p57Kip2 is required for the maturation of midbrain dopamine neuronal cells. Additional experiments in a dopaminergic cell line demonstrated that p57Kip2 can promote maturation by a mechanism that does not require p57Kip2-mediated inhibition of cyclin-dependent kinases. Instead, evidence indicates that p57Kip2 functions by a direct protein-protein interaction with Nurr1. Thus, in addition to its established function in control of proliferation, these results reveal a mechanism whereby p57Kip2 influences postmitotic differentiation of dopamine neurons.
Cip/Kip家族的细胞周期蛋白依赖性激酶抑制剂在胚胎发育过程中调节细胞增殖方面发挥着关键作用。然而,这些蛋白质还通过尚不清楚的机制影响细胞分化。在此我们表明,p57Kip2在有丝分裂后正在分化的中脑多巴胺能细胞中表达。p57Kip2表达的诱导依赖于Nurr1,一种对多巴胺神经元发育至关重要的孤儿核受体。此外,对p57Kip2基因敲除小鼠的分析表明,p57Kip2是中脑多巴胺能神经元细胞成熟所必需的。在多巴胺能细胞系中进行的其他实验表明,p57Kip2可通过一种不需要p57Kip2介导的对细胞周期蛋白依赖性激酶抑制作用的机制来促进成熟。相反,有证据表明p57Kip2通过与Nurr1直接的蛋白质-蛋白质相互作用发挥功能。因此,除了其在控制增殖方面已确定的功能外,这些结果揭示了一种p57Kip2影响多巴胺能神经元有丝分裂后分化的机制。