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Updated: May 16, 2026

Monitoring Astrocyte Reactivity and Proliferation in Vitro Under Ischemic-Like Conditions
Published on: October 21, 2017
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
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.
Background:
Depression and cerebrovascular disease influence each other, according to clinical studies. Despite this evidence, no studies have investigated the relationship between major depressive disorder (MDD) and cerebrovascular disease at the cellular level. Astrocytic processes are a crucial interface between blood vessels and neurons, and astrocyte density is reduced in MDD. This study investigated the coverage of vessels by astrocyte endfeet in the prefrontal cortex in MDD.
Methods:
Thirteen pairs of MDD and nonpsychiatric control subjects were used for double immunofluorescent staining and confocal image analysis. Frozen sections of gray matter from orbitofrontal area 47 and white matter from the ventromedial prefrontal cortex were examined. Astrocytic processes (labeled with antibodies for aquaporin-4 (AQP4) or glial fibrillary acidic protein were co-localized with blood vessels (labeled with an antibody to collagen IV) to measure the coverage of vessel walls by astrocyte processes.
Results:
The coverage of blood vessels by endfeet of AQP4-immunoreactive (IR) astrocytes was significantly reduced by 50% in subjects with MDD as compared with control subjects [analysis of covariance: F(1,23) = 5.161, p = .033]. This difference was detected in orbitofrontal gray matter but not in white matter. Conversely, the coverage of vessels by glial fibrillary acidic protein-IR processes did not significantly differ between the groups.
Conclusions:
A significant reduction in the coverage of gray matter vessels by AQP4-IR astrocyte processes in MDD suggests alterations in AQP4 functions such as regulation of water homeostasis, blood flow, glucose transport and metabolism, the blood-brain barrier, glutamate turnover, and synaptic plasticity.
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