Abstract
To investigate the involvement of galectin-3 in the process of neurodegeneration in prion diseases, the expression and cellular localization of galectin-3 in the brain were studied in scrapie, a mouse model of prion disease. Reverse transcription-polymerase chain reaction (RT-PCR) and Western blot analyses showed that the expression of galectin-3 protein and mRNA was induced in scrapie-affected brains, particularly at the time when the abnormal prion protein PrPSc began to accumulate in the brains. Immunohistochemically, immunostaining for galectin-3 was found mainly in B4-isolectin-positive cells (presumably activated microglia/macrophages), but not in astrocytes. Galectin-3 immunoreactivity was localized mainly in areas of PrPSc accumulation and neuronal death in scrapie-infected brains. These findings suggest that the expression of galectin-3 by activated microglia/macrophages in prion disease correlates with abnormal prion protein accumulation.
Original language | English |
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Pages (from-to) | 138-143 |
Number of pages | 6 |
Journal | Neuroscience Letters |
Volume | 420 |
Issue number | 2 |
DOIs | |
State | Published - 13 Jun 2007 |
Keywords
- Galectin-3
- Macrophage
- Microglia
- Prion disease
- Scrapie