Rotter A, Frostholm A
Brain Res Bull. 1986 Feb;16(2):205-14. doi: 10.1016/0361-9230(86)90034-1.
The distribution of 3H-mepyramine binding sites in cerebellae of normal mice and Purkinje cell degeneration, staggerer, weaver and reeler mutant mice was studied by light microscopic autoradiography. The binding of 3H-mepyramine to 20 micron coronal sections through the cerebellum and medulla had the characteristics expected of histamine-H1 receptor labeling. In the cerebellar cortex of normal mice, a high density of 3H-mepyramine binding was observed over the molecular layer and an intermediate density over the Purkinje cell layer, while the granule cell layer and white matter were almost devoid of labeling. The deep cerebellar nuclei were labeled to an intermediate density. In the 54 day old Purkinje cell degeneration mutant cerebellum, which is depleted of Purkinje cells, a greatly reduced labeling of the cerebellar cortex was observed. Labeling in the deep cerebellar nuclei was unaffected. In the 27 day old staggerer cerebellum, a mutation characterized by Purkinje cells which are almost devoid of spines and which do not form synaptic contacts with granule cells, a higher than normal grain density was seen over the cerebellar cortex, while normal grain density was observed over the deep cerebellar nuclei. The cerebellar cortex of 81 day old weaver mice, which is almost devoid of granule cells, had a high grain density over medial regions of the cortex, while the portion of the granule cell layer which remained relatively unaffected in the lateral parts of the cerebellum was unlabeled. The deep cerebellar nuclei had grain densities similar to littermate controls. In the 29 day old reeler cerebellae, which contain malpositioned Purkinje cells, high grain density regions corresponding to the heterotopically located Purkinje cells were observed. The present observations suggest that cerebellar cortical histamine-H1 receptors are associated predominantly with Purkinje cells. Furthermore, the expression of these H1 receptors appears not to be adversely affected by several alterations in the Purkinje cell environment, which have previously been shown to dramatically influence Purkinje cell morphology.
通过光学显微镜放射自显影术,研究了正常小鼠以及浦肯野细胞变性、蹒跚、织工和旋转突变小鼠小脑内3H-美吡拉敏结合位点的分布情况。3H-美吡拉敏与穿过小脑和延髓的20微米冠状切片的结合具有组胺-H1受体标记所预期的特征。在正常小鼠的小脑皮质中,分子层观察到高密度的3H-美吡拉敏结合,浦肯野细胞层为中等密度,而颗粒细胞层和白质几乎没有标记。小脑深部核团标记为中等密度。在54日龄的浦肯野细胞变性突变小鼠小脑中,由于浦肯野细胞缺失,观察到小脑皮质标记大大减少。小脑深部核团的标记不受影响。在27日龄的蹒跚小鼠小脑中,其特征是浦肯野细胞几乎没有树突棘且不与颗粒细胞形成突触联系,小脑皮质上可见高于正常的颗粒密度,而小脑深部核团观察到正常的颗粒密度。81日龄织工小鼠的小脑皮质几乎没有颗粒细胞,皮质内侧区域有高颗粒密度,而小脑外侧部分相对未受影响的颗粒细胞层部分未标记。小脑深部核团的颗粒密度与同窝对照相似。在29日龄的旋转小鼠小脑中,其浦肯野细胞位置异常,观察到与异位浦肯野细胞相对应的高颗粒密度区域。目前的观察结果表明,小脑皮质组胺-H1受体主要与浦肯野细胞相关。此外,这些H1受体的表达似乎不受浦肯野细胞环境中几种改变的不利影响,这些改变先前已被证明会显著影响浦肯野细胞形态。