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Updated: Oct 25, 2025

Ex Utero Electroporation and Organotypic Slice Culture of Mouse Hippocampal Tissue
Published on: March 4, 2015
Postnatal development of BAG3 expression in mouse cerebral cortex and hippocampus
Xinlu Li1, Geng Lin1, Tongtong Liu1,2
1Department of Histology and Embryology, China Medical University, Shenyang, 110122, China.
The protein BAG3 (Bcl2 associated athanogene 3) is crucial for autophagy. Its expression in mouse brains is stable until 12 months but significantly increases in aged mice, suggesting a role in aging-related neurodegeneration.
Area of Science:
- Neuroscience
- Molecular Biology
- Cellular Biology
Background:
- Autophagic processing declines in the aging central nervous system, potentially contributing to neurodegenerative diseases.
- BAG3 (Bcl2 associated athanogene 3) is a key co-molecular chaperone involved in selective macroautophagy.
Purpose of the Study:
- To investigate the expression and distribution of BAG3 in the brain across various developmental and aging stages in C57BL/6 mice.
Main Methods:
- Analysis of BAG3 mRNA and protein levels.
- Immunohistochemical examination of BAG3 distribution in the cerebral cortex and hippocampus.
Main Results:
- BAG3 mRNA and protein levels dropped significantly after birth (P0) but remained relatively stable from P15 to 12 months.
- A significant increase in BAG3 expression was observed in 18-month-old mice.
- Immunohistochemistry revealed BAG3 is primarily localized in neuronal cytoplasm and processes throughout postnatal development.
Conclusions:
- BAG3 expression is stable in young and middle-aged mice but becomes unstable in aged mice.
- The altered expression pattern of BAG3 in aging mice may have implications for neurodegenerative disease research.
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