Abstract

Very-KIND/Kndc1/KIAA1768 (v-KIND) is a brain-specific Ras guanine nucleotide exchange factor carrying two sets of the kinase non-catalytic C-lobe domain (KIND), and is predominantly expressed in cerebellar granule cells. Here, we report the impact of v-KIND deficiency on dendritic and synaptic growth in cerebellar granule cells in v-KIND knockout (KO) mice. Furthermore, we evaluate motor function in these animals. The gross anatomy of the cerebellum, including the cerebellar lobules, layered cerebellar cortex and densely-packed granule cell layer, in KO mice appeared normal, and was similar to wild-type (WT) mice. However, KO mice displayed an overgrowth of cerebellar granule cell dendrites, compared with WT mice, resulting in an increased number of dendrites, dendritic branches and terminals. Immunoreactivity for vGluT2 (a marker for excitatory presynapses of mossy fiber terminals) was increased in the cerebellar glomeruli of KO mice, compared with WT mice. The postsynaptic density around the terminals of mossy fibers was also increased in KO mice. Although there were no significant differences in locomotor ability between KO and WT animals in their home cages or in the open field, young adult KO mice had an increased grip strength and a tendency to exhibit better motor performance in balance-related tests compared with WT animals. Taken together, our results suggest that v-KIND is required for compact dendritic growth and proper excitatory synaptic connections in cerebellar granule cells, which are necessary for normal motor coordination and balance.

Highlights

  • The cerebellum plays a central role in motor learning [1]

  • Our findings indicate that v-kinase non-catalytic C-lobe domain (KIND) deficiency alters dendritic structure and excitatory synaptic connections in cerebellar granule cells

  • These results suggest that vKIND is required for normal, compact, dendritic growth in cerebellar granule cells, which is necessary for proper motor coordination and balance

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Summary

Introduction

The cerebellum plays a central role in motor learning [1]. The cerebellar cortex possesses five major types of neurons—Purkinje cells, basket cells, stellate cells, Golgi cells and granule cells [2]. Cerebellar granule cells are estimated to represent approximately half of all neurons in the brain, and their soma are densely packed in the granule cell layer. They extend an average of four short claw-like dendrites to form postsynapses around large mossy fiber terminals within the glomerular rosettes [4,5]. Cerebellar granule cells are electrically very compact, most likely because of their short and thin dendrites, which allows them to rapidly and accurately integrate the inputs from mossy fibers [6] Loss of these cells causes impairment in motor behavior [7,8,9, 10]. It is intriguing how cerebellar granule cells differentiate their unique dendritic structures

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