UMR-S 839, Inserm Paris, France.
Front Neuroanat. 2011 Jul 6;5:37. doi: 10.3389/fnana.2011.00037. eCollection 2011.
Striatal medium-sized spiny neurons (MSNs) receive massive glutamate inputs from the cerebral cortex and thalamus and are a major target of dopamine projections. Interaction between glutamate and dopamine signaling is crucial for the control of movement and reward-driven learning, and its alterations are implicated in several neuropsychiatric disorders including Parkinson's disease and drug addiction. Long-lasting forms of synaptic plasticity are thought to depend on transcription of gene products that alter the structure and/or function of neurons. Although multiple signal transduction pathways regulate transcription, little is known about signal transmission between the cytoplasm and the nucleus of striatal neurons and its regulation. Here we review the current knowledge of the signaling cascades that target the nucleus of MSNs, most of which are activated by cAMP and/or Ca(2+). We outline the mechanisms by which signals originating at the plasma membrane and amplified in the cytoplasm are relayed to the nucleus, through the regulation of several protein kinases and phosphatases and transport through the nuclear pore. We also summarize the identified mechanisms of transcription regulation and chromatin remodeling in MSNs that appear to be important for behavioral adaptations, and discuss their relationships with epigenetic regulation.
纹状体中型棘突神经元(MSNs)接收来自大脑皮层和丘脑的大量谷氨酸输入,是多巴胺投射的主要靶标。谷氨酸和多巴胺信号之间的相互作用对于运动控制和奖励驱动学习至关重要,其改变与包括帕金森病和药物成瘾在内的几种神经精神疾病有关。长时程形式的突触可塑性被认为依赖于改变神经元结构和/或功能的基因产物的转录。尽管有多种信号转导途径调节转录,但对于纹状体神经元细胞质和细胞核之间的信号传递及其调节知之甚少。在这里,我们回顾了针对 MSN 细胞核的信号级联的最新知识,其中大多数信号级联被 cAMP 和/或 Ca2+激活。我们概述了通过几种蛋白激酶和磷酸酶的调节以及通过核孔的运输,将源自质膜并在细胞质中放大的信号传递到细胞核的机制。我们还总结了 MSN 中似乎对行为适应很重要的转录调节和染色质重塑的机制,并讨论了它们与表观遗传调节的关系。