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Publication : Reduced mitochondria membrane potential and lysosomal acidification are associated with decreased oligomeric Aβ degradation induced by hyperglycemia: A study of mixed glia cultures.

First Author  Huang YC Year  2022
Journal  PLoS One Volume  17
Issue  1 Pages  e0260966
PubMed ID  35073330 Mgi Jnum  J:348711
Mgi Id  MGI:6861416 Doi  10.1371/journal.pone.0260966
Citation  Huang YC, et al. (2022) Reduced mitochondria membrane potential and lysosomal acidification are associated with decreased oligomeric Abeta degradation induced by hyperglycemia: A study of mixed glia cultures. PLoS One 17(1):e0260966
abstractText  Diabetes is a risk factor for Alzheimer's disease (AD), a chronic neurodegenerative disease. We and others have shown prediabetes, including hyperglycemia and obesity induced by high fat and high sucrose diets, is associated with exacerbated amyloid beta (Abeta) accumulation and cognitive impairment in AD transgenic mice. However, whether hyperglycemia reduce glial clearance of oligomeric amyloid-beta (oAbeta), the most neurotoxic Abeta aggregate, remains unclear. Mixed glial cultures simulating the coexistence of astrocytes and microglia in the neural microenvironment were established to investigate glial clearance of oAbeta under normoglycemia and chronic hyperglycemia. Ramified microglia and low IL-1beta release were observed in mixed glia cultures. In contrast, amoeboid-like microglia and higher IL-1beta release were observed in primary microglia cultures. APPswe/PS1dE9 transgenic mice are a commonly used AD mouse model. Microglia close to senile plaques in APPswe/PS1dE9 transgenic mice exposed to normoglycemia or chronic hyperglycemia exhibited an amoeboid-like morphology; other microglia were ramified. Therefore, mixed glia cultures reproduce the in vivo ramified microglial morphology. To investigate the impact of sustained high-glucose conditions on glial oAbeta clearance, mixed glia were cultured in media containing 5.5 mM glucose (normal glucose, NG) or 25 mM glucose (high glucose, HG) for 16 days. Compared to NG, HG reduced the steady-state level of oAbeta puncta internalized by microglia and astrocytes and decreased oAbeta degradation kinetics. Furthermore, the lysosomal acidification and lysosomal hydrolysis activity of microglia and astrocytes were lower in HG with and without oAbeta treatment than NG. Moreover, HG reduced mitochondrial membrane potential and ATP levels in mixed glia, which can lead to reduced lysosomal function. Overall, continuous high glucose reduces microglial and astrocytic ATP production and lysosome activity which may lead to decreased glial oAbeta degradation. Our study reveals diabetes-induced hyperglycemia hinders glial oAbeta clearance and contributes to oAbeta accumulation in AD pathogenesis.
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