Open AccessEuropium-Doped Cerium Oxide Nanoparticles for Microglial Amyloid Beta Clearance and Homeostasis
Author(s) -
Jatin Machhi,
Pravin Yeapuri,
Milica Marković,
Milankumar Patel,
Wenhui Yan,
Yaman Lu,
Jacob D. Cohen,
Mahmudul Hasan,
Mai Mohamed Abdelmoaty,
You Zhou,
Huangui Xiong,
Xinglong Wang,
R. Lee Mosley,
Howard E. Gendelman,
Bhavesh D. Kevadiya
Publication year - 2022
Publication title -
acs chemical neuroscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.158
H-Index - 69
ISSN - 1948-7193
DOI - 10.1021/acschemneuro.1c00847
Subject(s) - microglia , neuroinflammation , neurodegeneration , inflammation , chemistry , oxidative stress , amyloid beta , microbiology and biotechnology , scavenger receptor , immune system , medicine , immunology , biology , biochemistry , disease , cholesterol , peptide , lipoprotein
Alzheimer's disease (AD) is the most common neurodegenerative disorder. Pathologically, the disease is characterized by the deposition of amyloid beta (Aβ) plaques and the presence of neurofibrillary tangles. These drive microglia neuroinflammation and consequent neurodegeneration. While the means to affect Aβ plaque accumulation pharmacologically was achieved, how it affects disease outcomes remains uncertain. Cerium oxide (CeO 2 ) reduces Aβ plaques, oxidative stress, inflammation, and AD signs and symptoms. In particular, CeO 2 nanoparticles (CeO 2 NPs) induce free-radical-scavenging and cell protective intracellular signaling. This can ameliorate the pathobiology of an AD-affected brain. To investigate whether CeO 2 NPs affect microglia neurotoxic responses, a novel formulation of europium-doped CeO 2 NPs (EuCeO 2 NPs) was synthesized. We then tested EuCeO 2 NPs for its ability to generate cellular immune homeostasis in AD models. EuCeO 2 NPs attenuated microglia BV2 inflammatory activities after Aβ 1-42 exposure by increasing the cells' phagocytic and Aβ degradation activities. These were associated with increases in the expression of the CD36 scavenger receptor. EuCeO 2 NPs facilitated Aβ endolysosomal trafficking and abrogated microglial inflammatory responses. We posit that EuCeO 2 NPs may be developed as an AD immunomodulator.