Flavell Steven W, Greenberg Michael E
F.M. Kirby Neurobiology Center, Children's Hospital Boston, and Departments of Neurology and Neurobiology, Harvard Medical School, Boston, Massachusetts 02115, USA.
Annu Rev Neurosci. 2008;31:563-90. doi: 10.1146/annurev.neuro.31.060407.125631.
Sensory experience and the resulting synaptic activity within the brain are critical for the proper development of neural circuits. Experience-driven synaptic activity causes membrane depolarization and calcium influx into select neurons within a neural circuit, which in turn trigger a wide variety of cellular changes that alter the synaptic connectivity within the neural circuit. One way in which calcium influx leads to the remodeling of synapses made by neurons is through the activation of new gene transcription. Recent studies have identified many of the signaling pathways that link neuronal activity to transcription, revealing both the transcription factors that mediate this process and the neuronal activity-regulated genes. These studies indicate that neuronal activity regulates a complex program of gene expression involved in many aspects of neuronal development, including dendritic branching, synapse maturation, and synapse elimination. Genetic mutations in several key regulators of activity-dependent transcription give rise to neurological disorders in humans, suggesting that future studies of this gene expression program will likely provide insight into the mechanisms by which the disruption of proper synapse development can give rise to a variety of neurological disorders.
感觉体验以及大脑中由此产生的突触活动对于神经回路的正常发育至关重要。经验驱动的突触活动会导致膜去极化以及钙流入神经回路中的特定神经元,进而引发各种各样的细胞变化,这些变化会改变神经回路内的突触连接性。钙流入导致神经元形成的突触重塑的一种方式是通过激活新的基因转录。最近的研究已经确定了许多将神经元活动与转录联系起来的信号通路,揭示了介导这一过程的转录因子以及神经元活动调节基因。这些研究表明,神经元活动调节着一个复杂的基因表达程序,该程序涉及神经元发育的许多方面,包括树突分支、突触成熟和突触消除。活动依赖性转录的几个关键调节因子中的基因突变会导致人类出现神经疾病,这表明对该基因表达程序的未来研究可能会深入了解突触正常发育的破坏会引发各种神经疾病的机制。