Sawada Kazuhiko, Kalam Azad Abul, Sakata-Haga Hiromi, Lee Nam-Seob, Jeong Young-Gil, Fukui Yoshihiro
Department of Anatomy and Developmental Neurobiology, University of Tokushima Graduate School Institute of Health Biosciences, Tokushima, Japan.
Acta Neurobiol Exp (Wars). 2009;69(1):138-45. doi: 10.55782/ane-2009-1736.
Tottering mouse is an ataxic mutant that carries a mutation in a gene encoding for the apha1A subunit of P/Q-type Ca2+ channel (Cav2.1). This study revisited to examine whether a Purkinje cell loss occurred in the cerebellum of tottering mice. In tottering mice, Calbindin D-28k negative gaps were apparent in the vermis but not in the hemisphere. Calbindin D-28k immunofluorescence with DAPI staining demonstrated the absence of Purkinje cells in the Calbindin D-28k negative gaps. The Purkinje cell loss seemed to be observed prominently in the zebrin II negative compartments of the anterior vermis, but in the zebrin II positive compartments of the posterior vermis. Quite consistent with the histopathological observations, quantitation of the density of Calbindin D-28k and zebrin II immunopositive Purkinje cells in the tottering cerebellum revealed that the Purkinje cells were selectively lost in the zebrin II immunonegative compartments of the lobules I and II but in the zebrin II immunopositive compartments in the lobule IX. Those results predict that the susceptibility to the Cav2.1 gene defect is different among Purkinje cell phenotypes of the tottering cerebellum rather than the expression pattern of mutated Cav2.1 channels. This may result in the reproducible parasagittal pattern of Purkinje cell loss.
蹒跚小鼠是一种共济失调突变体,其编码P/Q型Ca2+通道(Cav2.1)的α1A亚基的基因发生了突变。本研究重新审视了蹒跚小鼠小脑是否发生浦肯野细胞丢失的情况。在蹒跚小鼠中,蚓部可见钙结合蛋白D-28k阴性间隙,而半球未见。钙结合蛋白D-28k免疫荧光与DAPI染色显示,钙结合蛋白D-28k阴性间隙中不存在浦肯野细胞。浦肯野细胞丢失似乎在前蚓部的zebrin II阴性区明显可见,但在后蚓部的zebrin II阳性区未见。与组织病理学观察结果非常一致,对蹒跚小鼠小脑中钙结合蛋白D-28k和zebrin II免疫阳性浦肯野细胞密度的定量分析表明,浦肯野细胞在小叶I和II的zebrin II免疫阴性区选择性丢失,但在小叶IX的zebrin II免疫阳性区未见丢失。这些结果预测,蹒跚小鼠小脑的浦肯野细胞表型对Cav2.1基因缺陷的易感性不同,而不是突变的Cav2.1通道的表达模式不同。这可能导致浦肯野细胞丢失呈现可重复的矢状旁区模式。