Abnormal kalirin signaling in neuropsychiatric disorders

Brain Res Bull. 2014 Apr:103:29-38. doi: 10.1016/j.brainresbull.2013.12.006. Epub 2013 Dec 12.

Abstract

Changes in dendritic spines structure and function play a critical role in a number of physiological processes, including synaptic transmission and plasticity, and are intimately linked to cognitive function. Alterations in dendritic spine morphogenesis occur in a number of neuropsychiatric disorders and likely underlie the cognitive and behavioral changes associated with these disorders. The neuronal guanine nucleotide exchange factor (GEF) kalirin is emerging as a key regulator of structural and functional plasticity at dendritic spines. Moreover, a series of recent studies have genetically and functionally linked kalirin signaling to several disorders, including schizophrenia and Alzheimer's disease. Kalirin signaling may thus represent a disease mechanism and provide a novel therapeutic target.

Keywords: Alzheimer's disease; Genetic; Glutamatergic; Mental disorder; Postmortem; Schizophrenia.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Review

MeSH terms

  • Alzheimer Disease / metabolism*
  • Animals
  • Guanine Nucleotide Exchange Factors / genetics
  • Guanine Nucleotide Exchange Factors / metabolism*
  • Humans
  • Mice
  • Mice, Knockout
  • Protein Serine-Threonine Kinases / metabolism*
  • Schizophrenia / metabolism*
  • Signal Transduction*

Substances

  • Guanine Nucleotide Exchange Factors
  • KALRN protein, mouse
  • KALRN protein, human
  • Protein Serine-Threonine Kinases