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Comparative study of aging in the mouse olfactory bulb.
Jennifer M Mirich1, Nathaniel C Williams, Daniel J Berlau
1Department of Psychology, University of Virginia, Charlottesville, Virginia 22904, USA.
The Journal of Comparative Neurology
|November 28, 2002
Summary
Mouse olfactory bulb structure and cell populations change with age, not just strain. Aged mice show increased volume and altered interneuron staining, with decreased cell proliferation and apoptosis.
Area of Science:
- Neuroscience
- Aging Research
- Olfactory System Biology
Background:
- Mice are key models for genetic research, but age and strain variations in their olfactory system are understudied.
- Understanding these differences is crucial for interpreting olfactory studies in mice.
Purpose of the Study:
- To investigate age-related and strain-specific changes in the mouse olfactory bulb.
- To compare mature and aged male mice across three common strains: BALB/cBy, C57BL/6J, and DBA/2.
Main Methods:
- Comparative analysis of olfactory bulb layer volumes (glomerular, external plexiform, mitral/granule cell).
- Immunohistochemistry for calretinin and tyrosine hydroxylase to assess interneuron populations.
- Glial fibrillary acidic protein staining to examine astrocyte morphology.
- Assessment of cell proliferation and apoptosis using specific labeling techniques.
Main Results:
- Olfactory bulb layer volumes increased with age, independent of body weight.
- Calretinin staining increased with age in C57BL/6J mice's external plexiform layer.
- Tyrosine hydroxylase staining patterns varied with age and strain, notably in old DBA/2 mice.
- Astrocytes were larger and more evenly distributed in C57BL/6J mice.
- Cell proliferation significantly decreased with age, with minimal activity in the rostral migratory stream.
- Apoptotic figures decreased in aged mice.
Conclusions:
- The mouse olfactory bulb undergoes significant age-related structural and cellular alterations.
- Strain differences exist in specific cell populations and astrocyte morphology.
- These age and strain variations must be considered when using mice as models for olfactory research.