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Reelin signaling in development, maintenance, and plasticity of neural networks

*Corresponding author for this work
Scholary Output:
Contribution to journal
Review article
Peer-review

Open access

Abstract

The developing brain is formed through an orchestrated pattern of neuronal migration, leading to the formation of heterogeneous functional regions in the adult. Several proteins and pathways have been identified as mediators of developmental neuronal migration and cell positioning. However, these pathways do not cease to be functionally relevant after the embryonic and early postnatal period; instead, they switch from guiding cells, to guiding synapses. The outcome of synaptic guidance determines the strength and plasticity of neuronal networks by creating a scalable functional architecture that is sculpted by cues from the internal and external environment. Reelin is a multifunctional signal that coordinates cortical and subcortical morphogenesis during development and regulates structural plasticity in adulthood and aging. Gain or loss of function in reelin or its receptors has the potential to influence synaptic strength and patterns of connectivity, with consequences for memory and cognition. The current review highlights similarities in the signaling cascades that modulate neuronal positioning during development, and synaptic plasticity in the adult, with a focus on reelin, a glycoprotein that is increasingly recognized for its dual role in the formation and maintenance of neural circuits.

Publication Information

Output type

Scholary Output:
Contribution to journal
Review article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 815-822 (8 pages)

Journal (Volume, Issue Number)

Ageing Research Reviews (Volume 12, Issue 3)

Publication milestones

  • Published - 06/2013

Publication status

Published - 06/2013

ISSN

1568-1637

Publication IDs

  • Scopus: 84881552864
  • PubMed: 23352928

Publication metrics

Metrics

Scopus
citations
SciVal
citations
51
SciVal
FWCI
1.34
SciVal
Author count
3
SciVal
Paper percentile
93
SciVal
Top percentile
10
Fractional count
2
Fractional count
0.67
Fractional count
1
Fractional count
0.33
Fractional count
2
Fractional count
1

PlumX, opens in new tab

Captures
137
Citation count
70

Funding Details

This work was supported by start-up funds from Georgia Health Sciences University and the authors have no conflict of interest.
FundersFunding number
Georgia Health Sciences University
-
NIA
F32AG034818