Single-Walled Carbon Nanotubes Alleviate Autophagic/Lysosomal Defects in Primary Glia from a Mouse Model of Alzheimer’s Disease
Author(s) -
Xue Xue,
Lirong Wang,
Yutaka Satō,
Ying Jiang,
Martin J. Berg,
DunSheng Yang,
Ralph A. Nixon,
XingJie Liang
Publication year - 2014
Publication title -
nano letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.853
H-Index - 488
eISSN - 1530-6992
pISSN - 1530-6984
DOI - 10.1021/nl501839q
Subject(s) - autophagy , neuroprotection , proteolysis , microbiology and biotechnology , pi3k/akt/mtor pathway , amyloid (mycology) , alzheimer's disease , amyloid precursor protein , lysosome , neuroscience , chemistry , disease , biology , apoptosis , medicine , signal transduction , biochemistry , pathology , inorganic chemistry , enzyme
Defective autophagy in Alzheimer's disease (AD) promotes disease progression in diverse ways. Here, we demonstrate impaired autophagy flux in primary glial cells derived from CRND8 mice that overexpress mutant amyloid precursor protein (APP). Functionalized single-walled carbon nanotubes (SWNT) restored normal autophagy by reversing abnormal activation of mTOR signaling and deficits in lysosomal proteolysis, thereby facilitating elimination of autophagic substrates. These findings suggest SWNT as a novel neuroprotective approach to AD therapy.
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