Kiyohara Yoshimoto, Endo Katsuaki, Ide Chizuka, Mizoguchi Akira
Department of Biological Sciences, Graduate School of Medicine, Kyoto University, Yoshida-konoe-cho, Sakyo-ku, Kyoto 606-8501, Japan.
J Electron Microsc (Tokyo). 2003;52(3):327-35. doi: 10.1093/jmicro/52.3.327.
To study morphologically the relationship between climbing fibre and Purkinje cell in the developing mouse cerebellum, we established a novel tract tracing using injection of 1,1'-dioctodecyl-3,3,3',3'-tetramethylindocarbocyanine perchlorate (DiI) into the inferior cerebellar peduncle, the half point of olivocerebellar projection. In this tracing method, only a certain number of climbing fibres were labelled with DiI and they revealed the single-fibre resolution, individually. These technical advantages enabled us to follow the projection of a climbing fibre to a Purkinje cell at the light microscopic level. To further investigate how a single labelled olivocerebellar axon interacts with a Purkinje cell, we introduced a photoconversion method into this tracing method and successfully observed the photo-oxidized climbing fibre terminals at the electron microscopic level. At postnatal days 7 and 9, a single DiI-labelled climbing fibre arborized around some adjacent Purkinje cell bodies in a distinguishable nest. At this pericellular nest stage, we first demonstrated that the terminal arborization stemmed from a single climbing fibre formed synapses simultaneously on both a soma and dendrites of a Purkinje cell. This finding suggests that the pericellular nest may be such an efficient form that a single climbing fibre innervates a Purkinje cell at both perisomatic and peridendritic sites. Thus, we succeeded in establishing an effective tracing method to investigate a single climbing fibre synaptogenesis with a Purkinje cell both at the light and electron microscopic levels.
为了从形态学上研究发育中小鼠小脑攀爬纤维与浦肯野细胞之间的关系,我们建立了一种新的示踪方法,即将高氯酸1,1'-二十八烷基-3,3,3',3'-四甲基吲哚羰花青(DiI)注入小脑下脚(橄榄小脑投射的中点)。在这种示踪方法中,只有一定数量的攀爬纤维被DiI标记,并且它们能单独显示单纤维分辨率。这些技术优势使我们能够在光学显微镜水平追踪一条攀爬纤维向浦肯野细胞的投射。为了进一步研究一条被标记的橄榄小脑轴突如何与浦肯野细胞相互作用,我们将光转换方法引入该示踪方法,并成功在电子显微镜水平观察到光氧化的攀爬纤维终末。在出生后第7天和第9天,一条被DiI标记的攀爬纤维在一些相邻的浦肯野细胞体周围形成分支,呈可区分的巢状。在这个细胞周巢阶段,我们首次证明源自单条攀爬纤维的终末分支同时在浦肯野细胞的胞体和树突上形成突触。这一发现表明,细胞周巢可能是一种有效的形式,使得单条攀爬纤维能在体细胞周围和树突周围位点支配浦肯野细胞。因此,我们成功建立了一种有效的示踪方法,可在光学显微镜和电子显微镜水平研究单条攀爬纤维与浦肯野细胞的突触形成。