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Review
. 1997 Jan;12(1):171-84.

Compartmentation of the granular layer of the cerebellum

Affiliations
  • PMID: 9046053
Review

Compartmentation of the granular layer of the cerebellum

K O Ozol et al. Histol Histopathol. 1997 Jan.

Abstract

Numerous studies have demonstrated that the cerebellum is highly compartmentalized. In most cases, compartmentation involves the Purkinje cells and the molecular layer, but there is also substantial evidence that the granular layer is subdivided into a large number of highly reproducible modules. We first review the evidence for a modular granular layer. Compartmentation of the granular layer has been revealed both functionally and structurally. First, tactile receptive field mapping has revealed numerous discrete functional modules within the granular layer. The molecular correlates of the receptive fields may be the compartments revealed by histological staining of the cerebellum for several enzymes and antigens. The structural substrate of the receptive fields is the mossy fiber afferent projection map, and anterograde tracing of various mossy fiber projections shows afferent terminals in parasagittal bands within the granular layer that are topographically aligned with the Purkinje cell compartments. Based on this evidence we argue that the cerebellum consists of many hundreds of reproducible structural/functional modules, and that a modular organization is a prerequisite for the efficient parallel processing of information during motor control. The complex organization of the adult granular layer implies elaborate developmental mechanisms. In the second part of the review we consider five developmental models to generate the modular organization of the adult granular layer: 1) the external granular layer is heterogeneous, and its topography translates directly into a modular granular layer; 2) granular layer modules are clones, derived from single external granular layer precursors; 3) modules in the granular layers are a secondary epigenetic response to the compartmentation of the Purkinje cells; 4) modules are secondary to the compartmentation of the afferent terminal fields; 5) modules are sculpted by activity-dependent processes.

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