Poluha W, Poluha D K, Chang B, Crosbie N E, Schonhoff C M, Kilpatrick D L, Ross A H
Worcester Foundation for Biomedical Research, Shrewsbury, Massachusetts 01545, USA.
Mol Cell Biol. 1996 Apr;16(4):1335-41. doi: 10.1128/MCB.16.4.1335.
We are employing recent advances in the understanding of the cell cycle to study the inverse relationship between proliferation and neuronal differentiation. Nerve growth factor and aphidicolin, an inhibitor of DNA polymerases, synergistically induce neuronal differentiation of SH-SY5Y neuroblastoma cells and the expression of p21WAF1, an inhibitor of cyclin-dependent kinases. The differentiated cells continue to express p21WAF1, even after removal of aphidicolin from the culture medium. The p21WAF1 protein coimmunoprecipitates with cyclin E and inhibits cyclin E-associated protein kinase activity. Each of three antisense oligonucleotides complementary to p21WAF1 mRNA partially blocks expression of p21WAF1 and promotes programmed cell death. These data indicate that p21WAF1 expression is required for survival of these differentiating neuroblastoma cells. Thus, the problem of neuronal differentiation can now be understood in the context of negative regulators of the cell cycle.
我们正在利用对细胞周期理解方面的最新进展来研究增殖与神经元分化之间的反比关系。神经生长因子和DNA聚合酶抑制剂阿非科林协同诱导SH-SY5Y神经母细胞瘤细胞的神经元分化以及细胞周期蛋白依赖性激酶抑制剂p21WAF1的表达。即使从培养基中去除阿非科林后,分化的细胞仍继续表达p21WAF1。p21WAF1蛋白与细胞周期蛋白E共免疫沉淀,并抑制细胞周期蛋白E相关的蛋白激酶活性。与p21WAF1 mRNA互补的三种反义寡核苷酸中的每一种都部分阻断p21WAF1的表达并促进程序性细胞死亡。这些数据表明p21WAF1的表达是这些分化的神经母细胞瘤细胞存活所必需的。因此,现在可以在细胞周期负调节因子的背景下理解神经元分化问题。