Coverage of blood vessels by astrocytic endfeet is reduced in major depressive disorder

Grazyna Rajkowska1, Jonathan Hughes, Craig A Stockmeier

  • 1Department of Psychiatry and Human Behavior, University of Mississippi Medical Center, Jackson, Mississippi 39216-4505, USA. grajkowska@umc.edu

Biological Psychiatry
|November 14, 2012
PubMed

Insights

Major depressive disorder (MDD) is linked to reduced astrocyte coverage of brain blood vessels. This cellular change in the prefrontal cortex may impact brain function in depression.

Area of Science:

  • Neuroscience
  • Cellular Biology
  • Psychiatry

Background:

  • Major depressive disorder (MDD) and cerebrovascular disease are clinically linked.
  • Previous research has not explored the cellular relationship between MDD and cerebrovascular disease.
  • Astrocyte density is decreased in MDD, impacting the neuron-blood vessel interface.

Purpose of the Study:

  • To investigate the coverage of blood vessels by astrocyte endfeet in the prefrontal cortex of individuals with MDD.
  • To examine cellular-level differences in astrocyte-blood vessel interactions in depression.

Main Methods:

  • Used double immunofluorescent staining and confocal microscopy on postmortem brain tissue from 13 MDD and 13 control subjects.
  • Examined orbitofrontal gray matter and ventromedial prefrontal white matter.
  • Quantified co-localization of astrocyte markers (aquaporin-4, glial fibrillary acidic protein) with blood vessel marker (collagen IV).

Main Results:

  • Significantly reduced coverage (50%) of gray matter blood vessels by aquaporin-4 (AQP4)-immunoreactive astrocyte endfeet in MDD subjects compared to controls (p=.033).
  • This reduction was specific to gray matter, not observed in white matter.
  • No significant difference in coverage by glial fibrillary acidic protein-immunoreactive astrocyte processes between groups.

Conclusions:

  • Reduced AQP4-astrocyte coverage in gray matter vessels of MDD patients indicates potential functional alterations.
  • These alterations may affect AQP4-mediated functions including water homeostasis, blood flow, and glucose metabolism.
  • Implications for blood-brain barrier integrity, glutamate turnover, and synaptic plasticity in MDD.
Abstract

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