Abstract

The mammalian cerebellum is located in the posterior cranial fossa and is critical for motor coordination and non-motor functions including cognitive and emotional processes. The anatomical structure of cerebellum is distinct with a three-layered cortex. During development, neurogenesis and fate decisions of cerebellar primordium cells are orchestrated through tightly controlled molecular events involving multiple genetic pathways. In this review, we will highlight the anatomical structure of human and mouse cerebellum, the cellular composition of developing cerebellum, and the underlying gene expression programs involved in cell fate commitments in the cerebellum. A critical evaluation of the cell death literature suggests that apoptosis occurs in ~5% of cerebellar cells, most shortly after mitosis. Apoptosis and cellular autophagy likely play significant roles in cerebellar development, we provide a comprehensive discussion of their role in cerebellar development and organization. We also address the possible function of unfolded protein response in regulation of cerebellar neurogenesis. We discuss recent advancements in understanding the epigenetic signature of cerebellar compartments and possible connections between DNA methylation, microRNAs and cerebellar neurodegeneration. Finally, we discuss genetic diseases associated with cerebellar dysfunction and their role in the aging cerebellum.

Highlights

  • Microscopic anatomy of the cerebellum was described in detail at the end of the 19th century by Ramon y Cajal and has attracted the attention of many researchers over the last century, and yet many questions remain unanswered

  • SUMMARY Anatomically, the cerebellum development begins at around E8 to E9 and cerebellar germinal zones are established during E9 to E13–14 in mice and the late embryonic period in humans The germinal zone can be categorized in four groups: internal germinal zone (VZ), external germinal zone (EGZ), caudomedial germinal zone and rostral germinal zone (RGZ)

  • Ventricular zone (VZ) is the source of Purkinje cells as well as all GABAergic interneurons in addition to a subset of non-neuronal cells

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Summary

Cellular commitment in the developing cerebellum

The anatomical structure of cerebellum is distinct with a three-layered cortex. Neurogenesis and fate decisions of cerebellar primordium cells are orchestrated through tightly controlled molecular events involving multiple genetic pathways. We will highlight the anatomical structure of human and mouse cerebellum, the cellular composition of developing cerebellum, and the underlying gene expression programs involved in cell fate commitments in the cerebellum. Apoptosis and cellular autophagy likely play significant roles in cerebellar development, we provide a comprehensive discussion of their role in cerebellar development and organization. We address the possible function of unfolded protein response in regulation of cerebellar neurogenesis. We discuss recent advancements in understanding the epigenetic signature of cerebellar compartments and possible connections between DNA methylation, microRNAs and cerebellar neurodegeneration. We discuss genetic diseases associated with cerebellar dysfunction and their role in the aging cerebellum

INTRODUCTION
Purkinje cells interneurons
EPIGENETIC MECHANISMS AND CEREBELLAR GENE EXPRESSION
Purkinje and granule cell death
Findings
Pontocerebellar hypoplasia
Full Text
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