mTOR signaling: at the crossroads of plasticity, memory and disease

Trends Neurosci. 2010 Feb;33(2):67-75. doi: 10.1016/j.tins.2009.11.003. Epub 2009 Dec 4.

Abstract

Mammalian target of rapamycin (mTOR) is a protein kinase involved in translation control and long-lasting synaptic plasticity. mTOR functions as the central component of two multi-protein signaling complexes, mTORC1 and mTORC2, which can be distinguished from each other based on their unique compositions and substrates. Although the majority of evidence linking mTOR function to synaptic plasticity comes from studies utilizing rapamycin, studies in genetically modified mice also suggest that mTOR couples receptors to the translation machinery for establishing long-lasting synaptic changes that are the basis for higher order brain function, including long-term memory. Finally, perturbation of the mTOR signaling cascade appears to be a common pathophysiological feature of human neurological disorders, including mental retardation syndromes and autism spectrum disorders.

Publication types

  • Review

MeSH terms

  • Animals
  • Gene Expression Regulation / physiology
  • Humans
  • Intracellular Signaling Peptides and Proteins / physiology*
  • Memory / physiology*
  • Mice
  • Models, Biological
  • Nervous System Diseases / genetics*
  • Neuronal Plasticity / physiology*
  • Protein Serine-Threonine Kinases / physiology*
  • Signal Transduction / physiology*
  • TOR Serine-Threonine Kinases

Substances

  • Intracellular Signaling Peptides and Proteins
  • MTOR protein, human
  • mTOR protein, mouse
  • Protein Serine-Threonine Kinases
  • TOR Serine-Threonine Kinases