Metzger Friedrich, Kapfhammer Josef P
Department of Medical Physiology, University of Groningen, Groningen, The Netherlands.
Cerebellum. 2003;2(3):206-14. doi: 10.1080/14734220310016150.
The cerebellum is a central organ in the control of motor learning and performance. In this respect, the cellular plasticity model systems of multiple climbing fiber elimination and long-term depression have been intensively studied. The signalling pathways involved in these plastic changes are now well understood on a molecular level and protein kinase C (PKC) activity appears to be crucially involved in both processes. Furthermore, as shown in recent studies, Purkinje cell dendritic development also critically depends on the activity of PKC. Thereby, the Ca(2+)-dependent PKC subtypes, activated by synaptic inputs through metabotropic glutamate receptors, trigger functional changes as well as long-term anatomical maturation of the Purkinje cell dendritic tree during cerebellar development at different time levels. This review summarizes these findings and forwards the hypothesis of a link between the functional mechanisms underlying LTD and the differentiation of Purkinje cell dendrites.
小脑是控制运动学习和表现的核心器官。在这方面,多个攀缘纤维消除和长时程抑制的细胞可塑性模型系统已得到深入研究。目前在分子水平上对这些可塑性变化所涉及的信号通路已了解得很清楚,蛋白激酶C(PKC)活性似乎在这两个过程中都起着关键作用。此外,如最近的研究所表明的,浦肯野细胞树突发育也严重依赖于PKC的活性。由此,由代谢型谷氨酸受体的突触输入激活的钙依赖性PKC亚型,在小脑发育的不同时间水平触发浦肯野细胞树突的功能变化以及长期的解剖学成熟。本综述总结了这些发现,并提出了长时程抑制的潜在功能机制与浦肯野细胞树突分化之间存在联系的假说。