Lin X, Cui H, Bulleit R F
Department of Pharmacology, University of Maryland School of Medicine, Baltimore 21201, USA.
Brain Res Dev Brain Res. 1998 Feb 10;105(2):277-86. doi: 10.1016/s0165-3806(97)00193-4.
This study reports that in purified cultures of postnatal cerebellar granule cells, BDNF significantly accelerated GABAA receptor alpha 6 subunit (GABAA alpha 6) mRNA expression, a marker for terminally differentiated cerebellar granule neurons, and also accelerated p21cip1 expression. p21cip1 is a general cyclin-dependent kinase (Cdk) inhibitor that can inhibit progression through the cell cycle. Alternatively, the expression of p27kip1, another Cdk inhibitor closely related to p21cip1, is not modified by BDNF. In cultured granule cells, the increase in p21cip1 expression induced by BDNF occurred after dividing granule cells had left the cell cycle and thus was not required to direct granule neuron precursors out of the cell cycle. p21cip1 may have an alterative function during granule neuron terminal differentiation, separate from its ability to regulate cell cycle exit. This report shows that, in vitro, BDNF accelerates granule cell gene expression and may thus modulate cerebellar granule cell differentiation.
本研究报告称,在出生后小脑颗粒细胞的纯化培养物中,脑源性神经营养因子(BDNF)显著加速了γ-氨基丁酸A型受体α6亚基(GABAAα6)mRNA的表达,这是终末分化的小脑颗粒神经元的一个标志物,并且还加速了p21cip1的表达。p21cip1是一种通用的细胞周期蛋白依赖性激酶(Cdk)抑制剂,可抑制细胞周期进程。另外,与p21cip1密切相关的另一种Cdk抑制剂p27kip1的表达不受BDNF的影响。在培养的颗粒细胞中,BDNF诱导的p21cip1表达增加发生在分裂的颗粒细胞离开细胞周期之后,因此并非引导颗粒神经元前体细胞退出细胞周期所必需的。p21cip1在颗粒神经元终末分化过程中可能具有一种与其调节细胞周期退出能力不同的功能。本报告表明,在体外,BDNF可加速颗粒细胞基因表达,从而可能调节小脑颗粒细胞的分化。