| First Author | Lin A | Year | 2020 |
| Journal | J Neuroinflammation | Volume | 17 |
| Issue | 1 | Pages | 254 |
| PubMed ID | 32861245 | Mgi Jnum | J:295173 |
| Mgi Id | MGI:6458177 | Doi | 10.1186/s12974-020-01924-z |
| Citation | Lin A, et al. (2020) Serum amyloid A inhibits astrocyte migration via activating p38 MAPK. J Neuroinflammation 17(1):254 |
| abstractText | BACKGROUND: The accumulation of astrocytes around senile plaques is one of the pathological characteristics in Alzheimer's disease (AD). Serum amyloid A (SAA), known as a major acute-phase protein, colocalizes with senile plaques in AD patients. Here, we demonstrate the role of SAA in astrocyte migration. METHODS: The effects of SAA on astrocyte activation and accumulation around amyloid beta (Abeta) deposits were detected in APP/PS1 transgenic mice mated with Saa3(-/-) mice. SAA expression, astrocyte activation, and colocalization with Abeta deposits were evaluated in mice using immunofluorescence staining and/or Western blotting. The migration of primary cultures of mouse astrocytes and human glioma U251 cells was examined using Boyden chamber assay and scratch-would assay. The actin and microtubule networks, protrusion formation, and Golgi apparatus location in astrocytes were determined using scratch-would assay and immunofluorescence staining. RESULTS: Saa3 expression was significantly induced in aged APP/PS1 transgenic mouse brain. Saa3 deficiency exacerbated astrocyte activation and increased the number of astrocytes around Abeta deposits in APP/PS1 mice. In vitro studies demonstrated that SAA inhibited the migration of primary cultures of astrocytes and U251 cells. Mechanistic studies showed that SAA inhibited astrocyte polarization and protrusion formation via disrupting actin and microtubule reorganization and Golgi reorientation. Inhibition of the p38 MAPK pathway abolished the suppression of SAA on astrocyte migration and polarization. CONCLUSIONS: These results suggest that increased SAA in the brain of APP/PS1 mice inhibits the migration of astrocytes to amyloid plaques by activating the p38 MAPK pathway. |
