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Physiological application of nanoparticles in calcium-related proteins and channels

Authors
Lee, DongunHong, Jeong Hee
Issue Date
Sep-2019
Publisher
FUTURE MEDICINE LTD
Keywords
Ca2+ ATPase; Ca2+ signaling; cytotoxicity; G protein-coupled receptors; nanoparticles; signal transduction; store-operated Ca2+ channels; transient receptor potential channels; voltage-gated Ca2+ channels
Citation
NANOMEDICINE, v.14, no.18, pp.2479 - 2486
Journal Title
NANOMEDICINE
Volume
14
Number
18
Start Page
2479
End Page
2486
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/18233
DOI
10.2217/nnm-2019-0004
ISSN
1743-5889
Abstract
Nanoparticles (NPs) have been studied as therapeutic drug-delivery agents for promising clinical trial outcomes. Nanomaterial-based drugs can transfer conventional drugs to target lesions, such as tumors, with increasing efficiency by enhancing drug-cell interaction or drug absorption. Although they are favorable as efficient drug transfer systems, NPs also exhibit cytotoxicity that affects nonpathological regions. Here, we review the basic information behind NP-induced Ca2+ signaling and its participation in channel physiology and pathology. NPs are observed to demonstrate inhibitory or active effects on Ca2+ signaling. Thus, understanding Ca2+ signaling by NPs as a key mechanism in signal transduction will progress the application of nano-drugs in various diseases without deleterious effect.
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