| Literature DB >> 33472003 |
Insung Kang1,2, Je Min Yoo3,4, Donghoon Kim5, Juhee Kim3, Myung Keun Cho3, Seung-Eun Lee1,2, Dong Jin Kim6, Byung-Chul Lee1,2, Jin Young Lee1,2, Jae-Jun Kim1,2, Nari Shin1,2, Soon Won Choi1,2, Young-Ho Lee7,8,9, Han Seok Ko10, Seokmin Shin3, Byung Hee Hong3,5,6, Kyung-Sun Kang1,2.
Abstract
While the neuropathological characteristics of Niemann-Pick disease type C (NPC) result in a fatal diagnosis, the development of clinically available therapeutic agent remains a challenge. Here we propose graphene quantum dots (GQDs) as a potential candidate for the impaired functions in NPC in vivo. In addition to the previous findings that GQDs exhibit negligible long-term toxicity and are capable of penetrating the blood-brain barrier, GQD treatment reduces the aggregation of cholesterol in the lysosome through expressed physical interactions. GQDs also promote autophagy and restore defective autophagic flux, which, in turn, decreases the atypical accumulation of autophagic vacuoles. More importantly, the injection of GQDs inhibits the loss of Purkinje cells in the cerebellum while also demonstrating reduced activation of microglia. The ability of GQDs to alleviate impaired functions in NPC proves the promise and potential of the use of GQDs toward resolving NPC and other related disorders.Entities:
Keywords: Niemann-pick disease type C; cholesterol accumulation; graphene quantum dots; lysosomal storage disorders; nanomedicine
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Year: 2021 PMID: 33472003 DOI: 10.1021/acs.nanolett.0c03741
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189