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Published on: December 29, 2014
Long-term environmental enrichment reduces microglia morphological diversity of the molecular layer of dentate gyrus
Thaís Cristina Galdino de Oliveira1, Dario Carvalho-Paulo1, Camila Mendes de Lima1
1Laboratório de Investigações em Neurodegeneração e Infecção, Instituto de Ciências Biológicas, Hospital Universitário João de Barros Barreto, Universidade Federal do Pará, Belém, Brasil.
Abstract:
We investigated long-term environmental influences on morphology of microglia from the outer and middle thirds of molecular layer of the dentate gyrus (MolDG), and on microglia from dorsal and ventral dentate gyrus molecular layer. We also estimated the total number of MolDG microglia using stereology. For this purpose, microglia of the molecular layer of the dentate gyrus of 20-month-old female Swiss albino mice, housed from 21st postnatal day onwards, in the impoverished environment of the standard laboratory cages (SEA), or in a cage with an enriched environment (EEA), were reconstructed microscopically in three dimensions and compared with each other and with microglia of 6-month-old female Swiss albino mice, also housed from weaning onwards in an enriched cage (EEY). All mice had their brains sectioned and processed for immunolabeling for IBA-1, a selective microglia marker. Random and systematic microglia samples were reconstructed in three dimensions and classified morphologically using hierarchical cluster analysis, followed by discriminant function analysis. SEA and EEY showed two morphological phenotypes of microglia in both the outer and middle thirds of MolDG. EEA mice showed such a reduction in the morphological diversity of microglia that essentially a single morphotype was found. EEA mouse microglia showed an intermediate morphological complexity between types I and II SE microglia. We suggest that type I and type II microglia in SE mice may have different physiological roles and that long-term EE may be associated with adaptive responses of microglial phenotypes to somatomotor and cognitive stimuli.
Insights
Long-term environmental enrichment significantly reduced microglial morphological diversity in the dentate gyrus molecular layer. Enriched environments may promote adaptive microglial phenotypes for cognitive and somatomotor stimuli.
Area of Science:
- Neuroscience
- Neuroimmunology
- Cell Biology
Background:
- Microglia, the resident immune cells of the brain, play crucial roles in neural development and function.
- Environmental factors are known to influence brain plasticity and cellular behavior.
- Understanding microglial responses to environmental stimuli is vital for comprehending brain health and disease.
Purpose of the Study:
- To investigate the long-term effects of environmental enrichment on microglial morphology in the dentate gyrus molecular layer.
- To compare microglial phenotypes in standard (impoverished) and enriched environments across different ages.
- To assess the impact of environmental enrichment on microglial diversity and potential functional roles.
Main Methods:
- Three-dimensional reconstruction and morphological analysis of microglia (IBA-1 labeled) from Swiss albino mice housed in standard (SEA) or enriched (EEA) environments.
- Stereological estimation of microglial numbers in the molecular layer of the dentate gyrus.
- Hierarchical cluster analysis and discriminant function analysis for morphological classification.
Main Results:
- Standard environment (SEA) and young enriched environment (EEY) housing revealed two distinct microglial morphological phenotypes in the MolDG.
- Long-term environmental enrichment (EEA) significantly reduced microglial morphological diversity, resulting in a predominant single morphotype.
- Microglia in the EEA exhibited intermediate morphological complexity between the two phenotypes observed in SE mice.
Conclusions:
- Distinct microglial phenotypes in standard environments may indicate specialized physiological roles.
- Long-term environmental enrichment appears to induce adaptive changes in microglial phenotypes.
- These adaptive microglial responses may be associated with enhanced processing of somatomotor and cognitive stimuli.
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