Serotonin transporter gene, stress and raphe-raphe interactions: a molecular mechanism of depression

Trends Neurosci. 2012 Jul;35(7):395-402. doi: 10.1016/j.tins.2012.01.001. Epub 2012 Jan 31.

Abstract

Reports of gene-environment interactions (GxE) between the serotonin transporter gene and stress on risk of depression have generated both excitement and controversy. The controversy persists in part because a mechanistic account of this GxE on serotonergic neurotransmission and risk of depression has been lacking. In this Opinion, we draw on recent discoveries in the functional neuroanatomy of the serotonergic dorsal raphe nucleus (DR) to propose such a mechanistic account. We argue that genetically produced variability in serotonin reuptake during stressor-induced raphe-raphe interactions alters the balance in the amygdala-ventromedial prefrontal cortex (VMPFC)-DR circuitry underlying stressor reactivity and emotion regulation. In particular, the recently characterized stressor-responsive serotonergic interneurons originating from the dorsolateral DR may hold a key to unlocking the GxE mechanism of depression.

MeSH terms

  • Animals
  • Depression / etiology*
  • Gene-Environment Interaction*
  • Genetic Predisposition to Disease / genetics
  • Humans
  • Raphe Nuclei*
  • Serotonin Plasma Membrane Transport Proteins / genetics*
  • Stress, Psychological / genetics*

Substances

  • Serotonin Plasma Membrane Transport Proteins