Landis D M, Sidman R L
J Comp Neurol. 1978 Jun 15;179(4):831-63. doi: 10.1002/cne.901790408.
Postnatal development of the cerebellar cortex has been compared in staggerer mutant and unaffected littermate mice. From postnatal day 3 to about day 21 the external granular layer in staggerer mice is decreased in thickness and area, and the number of postmitotic granule cell neurons is reduced. Those granule cells that are generated seem to differentiate normally, with the remarkable exception that they form only primitive junctions with Purkinje cell dendritic shafts. These specialized junctions are not superseded by the normal parallel fiber:Purkinje spine synapses and disappear by the third week. Purkinje cell somata and dendrites are smaller than normal at all stages examined. The dendrites are not confined to the sagittal plane as in the normal and, unique among mutant or other animals described to date, they exhibit virtually no branchlet spines. All other cortical synaptic relations of granule and Purkinje cells, including climbing fiber:Purkinje spine synapses, appear qualitatively normal. However, by 28 days virtually all staggerer granule cells have degenerated. While the primary genetic defect remains unknown, we postulate that the morphological abnormalities may be attributable to a block in the normal developmental relationship between granule cells and Purkinje cells. The small cell size and failure to form branchlet spines suggest that the Purkinje cell abnormality may be closer to the primary effect of the mutant gene than the more flagrant hypoplasia and degeneration of granule cell neurons.
在蹒跚突变小鼠和未受影响的同窝小鼠中,对小脑皮质的产后发育进行了比较。从出生后第3天到大约第21天,蹒跚小鼠的外颗粒层厚度和面积减小,有丝分裂后颗粒细胞神经元数量减少。那些产生的颗粒细胞似乎正常分化,但有一个显著例外,即它们仅与浦肯野细胞树突轴形成原始连接。这些特殊连接不会被正常的平行纤维:浦肯野棘突触取代,并在第三周消失。在所有检查阶段,浦肯野细胞的胞体和树突都比正常的小。树突不像正常情况那样局限于矢状面,而且在迄今为止描述的突变体或其他动物中独一无二的是,它们几乎没有小分支棘。颗粒细胞和浦肯野细胞的所有其他皮质突触关系,包括攀缘纤维:浦肯野棘突触,在质量上看起来正常。然而,到28天时,几乎所有蹒跚小鼠的颗粒细胞都已退化。虽然主要的基因缺陷仍然未知,但我们推测形态学异常可能归因于颗粒细胞和浦肯野细胞之间正常发育关系的阻断。细胞体积小和未能形成小分支棘表明,浦肯野细胞异常可能比颗粒细胞神经元更明显的发育不全和退化更接近突变基因的主要作用。