Recent association studies indicate several genes highly expressed by microglia influence Alzheimer’s disease (AD) risk, which suggests microglial function contributes to this disease. Here, we evaluated how one component of microglial function, cytokine release, affects AD-related phenomena. First, we used a 3-hour lipopolysaccharide (LPS) treatment to activate mouse BV2 microglial cells. Next, we removed the LPS-containing medium, added LPS-free medium, and after 6 hours collected the medium conditioned by the activated BV2 microglial cells. We then exposed human neuronal SH-SY5Y cells to the conditioned medium for 24 hours. At the end of the 24-hour exposure, we assessed amyloid-β protein precursor (AβPP), tau, apolipoprotein E (ApoE), and lipid status. The amount of AβPP was unaffected, although a slight decrease in soluble AβPPα suggested a subtle reduction in AβPP non-amyloidogenic processing occurred. Tau mRNA increased, but total and phosphorylated tau levels were unchanged. ApoE mRNA increased, while ApoE protein levels were lower. Per cell lipid droplet number decreased and lipid oxidation increased. These results show cytokine release by activated microglial cells can influence specific AD-relevant physiologies and pathologies.
Effects of Microglial Cytokines on Alzheimer’s Disease-Related Phenomena
Yan Ji,Xiaowan Wang,Colin H. Kalicki,B. Menta,Megan Baumgardner,Scott J Koppel,Ian W. Weidling,Judit Perez-Ortiz,Heather M. Wilkins,R. Swerdlow
Published 2019 in Journal of Alzheimer's Disease
ABSTRACT
PUBLICATION RECORD
- Publication year
2019
- Venue
Journal of Alzheimer's Disease
- Publication date
2019-01-28
- Fields of study
Biology, Medicine, Chemistry, Psychology
- Identifiers
- External record
- Source metadata
Semantic Scholar, PubMed
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