REELER encyclopedia topics

REELER - 2 reference results

The reeler is an autosomal recessive mouse mutant, in which cortical neurons are generated normally but are abnormally placed, resulting in disorganization of cortical laminar layers in the CNS. The reason is the lack of Reelin, an extracellular matrix glycoprotein, which during the corticogenesis is secreted mainly by the Cajal-Retzius cells. In the reeler neocortex, cortical plate neurons are aligned in a practically inverted fashion (‘‘outside-in’’). The name "reeler" comes from the distinct “reeling” gait that is caused by profound hypoplasia of the mouse cerebellum, in which the normal cerebellar folia are missing. In the ventricular zone of the cortex fewer neurons have been found to have radial glial processes. In the dentate gyrus of hippocampus, no characteristic radial glial scaffold is formed and no compact granule cell layer is established. Therefore, the reeler mouse presents a good model in which to investigate the mechanisms of establishment of the precise neuronal network during development.

There are two types of the reeler mutation:

Albany2 mutation (Reln(rl-Alb2)
- Orleans mutation (Reln-rl-orl, or rl-orl), in which reelin lacks a C-terminal region and a part of the eighth reelin repeat. This hampers the secretion of the protein from the cell.
  
  Key pathological findings in the Reeler brain structure
  - Inversion of cortical layers.
  - Dispersion of neurons within cortical layers.
  - Decreased cerebellar size.
  - Failure of preplate to split
  - Failure to establish a distinct granule cell layer in the dentate gyrus. Normal dentate gyrus demonstrates a clear segregation of granule cells and hilar mossy cells, which are identified, respectively, by their expression of calbindin and calretinin. In the reeler DG, the two cell types intermingle.
    - Impaired dendrite outgrowth.
      - In one study, reeler mice were shown to have attenuated methamphetamine-induced hyperlocomotion, which was also reduced by a targeted disruption of reelin activity in wildtype mice. Reeler mice in the same study demonstrated a decrease in D1 and D2 receptor-mediated dopaminergic function together with reduced numbers of D1D2 receptors.
        Heterozygous Reeler Mouse
        Heterozygous reeler mice, also known as HRM, while lacking the apparent phenotype seen in the homozygous reeler, also show some brain abnormalities due to the reelin deficit.
        Heterozygous (rl/+) mice express reelin at 50% of wild-type levels and have grossly normal brains but exhibit a progressive loss during aging of a neuronal target of reelin action, Purkinje cells.
        Studies reveal a 16% deficit in the number of Purkinje cells in 3-month-old (+/rl) and a 24% one in 16-month-old animals: surprisingly this deficit is only present in the (+/rl) males, while the females are spared.
        History of research
        First mention of reeler mouse mutation dates back to 1951. In the later years, histopathological studies revealed that the reeler cerebellum is dramatically decreased in size and the normal laminar organization found in several brain regions is disrupted (Hamburgh, 1960). In 1995, the RELN gene and reelin protein were discovered at chromosome 7q22 by Gabriella D'Arcangelo and colleagues. .
        See also
        Shaking rat Kawasaki has a reduced reelin expression due to missplicing of the reelin gene.
        External links
        Development of the Cerebral Cortex: III. The Reeler Mutation - by Paul J. Lombroso, M.D.
        References