Affiliations: [a] Department of Neurology, Zhongshan Hospital, State Key Laboratory of Medical Neurobiology, Institutes of Brain Science, Fudan University, Shanghai, China
| [b]
Department of Neurology, Xiamen Branch Zhongshan Hospital, Fudan University, Xiamen, China
Correspondence:
[*]
Correspondence to: Xiaoqin Cheng and Chunjiu Zhong, Department of Neurology, Zhongshan Hospital, Fudan University, 136 Yixueyuan Road, Xuhui District, Shanghai, 200032, China. Tel.: +86 21 54237920; E-mails: [email protected] (XC); [email protected] (CZ).
Note: [1] These authors contributed equally to this work.
Abstract: Background:Microglia play diverse roles in Alzheimer’s disease (AD). Intracellular metabolism has been indicated an important factor in modulating the function of microglia. However, it is not clear whether the intracellular metabolism of microglia changes dynamically in different stages of AD. Objective:To determine whether microglia intracellular metabolism changes dynamically in different stages of AD. Methods:Microglia were extracted from APPSwe/PS1dE9 (APP/PS1) mice and wild-type littermates at 2, 4, and 8 months old by fluorescence-activated cell sorting and used for RNA-sequencing analysis and quantitative PCR. Morphologies of amyloid plaques and microglia were detected by immunofluorescence staining. Results:Compared with control littermates, the microglia of APP/PS1 mice exhibited significant transcriptional changes at 2-month-old before microglia morphological alterations and the plaque formation. The changes continued drastically following age with defined morphological shift of microglia and amyloid plaque enhancement in brains. Further analysis of those genotype and age dependent transcriptomic changes revealed that differentially expressed genes were enriched in pathways related to energy metabolism. Compared with wild-type mice, there were changes of some vital genes related to glucose metabolism and lipid metabolism pathways in APP/PS1 mice at different ages. Glucose metabolism may play a major role in early activation of microglia, and lipid metabolism may be more important in later activation period. Conclusion:Our results showed that microglia actively participate in the pathological progress of AD. The intracellular metabolism of microglia changed significantly in different stages of AD, even preceding amyloid-β deposition.
