Abstract

APOE4 is a major risk factor for sporadic Alzheimer’s disease; however, it is unclear how it exerts its pathological effects. Others and we have previously shown that autophagy is impaired in APOE4 compared to APOE3 astrocytes, and demonstrated differences in the expression of mitochondrial dynamics proteins in brains of APOE3 and APOE4 transgenic mice. Here, we investigated the effect of APOE4 expression on several aspects of mitochondrial function and network dynamics, including fusion, fission, and mitophagy, specifically in astrocytes. We found that APOE3 and APOE4 astrocytes differ in their mitochondrial dynamics, suggesting that the mitochondria of APOE4 astrocytes exhibit reduced fission and mitophagy. APOE4 astrocytes also show impaired mitochondrial function. Importantly, the autophagy inducer rapamycin enhanced mitophagy and improved mitochondrial functioning in APOE4 astrocytes. Collectively, the results demonstrate that APOE4 expression is associated with altered mitochondrial dynamics, which might lead to impaired mitochondrial function in astrocytes. This, in turn, may contribute to the pathological effects of APOE4 in Alzheimer’s disease.

Highlights

  • Alzheimer’s disease (AD) is characterized by brain Aβ plaques and neurofibrillary tangles, neuronal loss and cognitive decline

  • Changes in mitochondrial dynamics and mitochondrial dysfunction are recognized as hallmarks of AD, and mitochondrial deterioration in astrocytes occurs early in the disease development, the mechanism is vague[12]

  • It was shown that APOE4 is associated with impaired autophagy in astrocytes[13,14], as well as with changes in mitochondrial dynamics proteins expression in transgenic mice brains[15]

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Summary

Introduction

Alzheimer’s disease (AD) is characterized by brain Aβ plaques and neurofibrillary tangles, neuronal loss and cognitive decline. Mitochondrial dynamics include fusion, fission, and degradation events, linked to mitochondrial function[3,4]. Damaged mitochondria are degraded by selective autophagy, termed mitophagy, Several proteins are required for mitochondrial fusion, including the mitofusins (Mfn1/Mfn2)[3,4]. This process is triggered by increased mitochondrial membrane potential (MMP) and involves the oligomerization of mitofusins on the outer mitochondrial membrane (OMM)[4]. Mitophagy proceeds mitochondrial fission and is triggered by decreased MMP5 It allows the removal of damaged/excessive mitochondria via the lysosome.

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