Seil Fredrick J
Department of Neurology, Oregon Health & Science University, Portland, OR, USA.
Neurosci Biobehav Rev. 2014 Sep;45:212-32. doi: 10.1016/j.neubiorev.2014.06.003. Epub 2014 Jun 13.
Circuit reorganization after injury was studied in a cerebellar culture model. When cerebellar cultures derived from newborn mice were exposed at explantation to a preparation of cytosine arabinoside that destroyed granule cells and oligodendrocytes and compromised astrocytes, Purkinje cells surviving in greater than usual numbers were unensheathed by astrocytic processes and received twice the control number of inhibitory axosomatic synapses. Purkinje cell axon collaterals sprouted and many of their terminals formed heterotypical synapses with other Purkinje cell dendritic spines. The resulting circuit reorganization preserved inhibition in the cerebellar cortex. Following this reorganization, replacement of the missing granule cells and glia was followed by a restitution of the normal circuitry. Most of these developmental and reconstructive changes were not dependent on neuronal activity, the major exception being inhibitory synaptogenesis. The full complement of inhibitory synapses did not develop in the absence of neuronal activity, which could be mitigated by application of exogenous TrkB receptor ligands. Inhibitory synaptogenesis could also be promoted by activity-induced release of endogenous TrkB receptor ligands or by antibody activation of the TrkB receptor.
在小脑培养模型中研究了损伤后的回路重组。当将新生小鼠来源的小脑培养物在植入时暴露于一种阿糖胞苷制剂,该制剂破坏颗粒细胞和少突胶质细胞并损害星形胶质细胞时,存活数量多于正常的浦肯野细胞未被星形胶质细胞突起包裹,并接受了两倍于对照数量的抑制性轴体突触。浦肯野细胞轴突侧支发芽,其许多终末与其他浦肯野细胞树突棘形成异型突触。由此产生的回路重组保留了小脑皮质中的抑制作用。在这种重组之后,缺失的颗粒细胞和神经胶质细胞被替代,随后正常回路得以恢复。这些发育和重建变化大多不依赖于神经元活动,主要的例外是抑制性突触形成。在没有神经元活动的情况下,抑制性突触的完整补充并未发育,这可以通过应用外源性TrkB受体配体来缓解。抑制性突触形成也可以通过活性诱导的内源性TrkB受体配体释放或通过TrkB受体的抗体激活来促进。