Glycyrrhizic acid prevents astrocyte death by neuromyelitis optica-specific IgG via inhibition of C1q binding

Authors
Kim, Ji-SunCheon, SoyoungKim, Seung WooKim, BoramKim, HeejaungPark, Ki DukKim, Sung-Min
Issue Date
2016-09-16
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
Citation
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.478, no.2, pp.553 - 558
Abstract
Neuromyelitis optica (NMO) is an inflammatory demyelinating disease of the central nervous system and is mediated by complement-dependent cytotoxicity (CDC) of NMO-specific immunoglobulin G (IgG) antibodies (NMO-IgG). Glycyrrhizic acid (GA) has numerous pharmacological effects including inhibition of the complement pathway. We aimed to study the influence of GA on NMO-IgG-induced CDC. NMO-IgG samples from 7 patients with NMO, together with human complement, induced CDC in an aquaporin 4 M23-overexpressing glial cell line, an in vitro NMO model. GA attenuated NMO-IgG-induced CDC in a dose-dependent manner. The mechanism of the GA-related CDC inhibition was sequentially dissected and found to involve inhibition of C1q binding to NMO-IgG. Consequently, GA attenuates NMO-IgG-induced CDC and may be a promising novel therapeutic agent against NMO. (C) 2016 Elsevier Inc. All rights reserved.
Keywords
COMPLEMENT-DEPENDENT CYTOTOXICITY; MULTIPLE-SCLEROSIS; RETROSPECTIVE ANALYSIS; DIAGNOSTIC-CRITERIA; SPECTRUM DISORDERS; WATER CHANNEL; IN-VITRO; MARKER; THERAPIES; PROTEIN; COMPLEMENT-DEPENDENT CYTOTOXICITY; MULTIPLE-SCLEROSIS; RETROSPECTIVE ANALYSIS; DIAGNOSTIC-CRITERIA; SPECTRUM DISORDERS; WATER CHANNEL; IN-VITRO; MARKER; THERAPIES; PROTEIN; Glycyrrhizic acid; Neuromyelitis optica; Complement dependent cytotoxicity
ISSN
0006-291X
URI
https://pubs.kist.re.kr/handle/201004/123669
DOI
10.1016/j.bbrc.2016.07.098
Appears in Collections:
KIST Article > 2016
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE