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Mycophenolic acid inhibits oleic acid-induced mesangial cell activation through both cellular reactive oxygen species and inosine monophosphate dehydrogenase 2 pathways

Authors
 Kyu Ha Huh  ;  Hyung Joon Ahn  ;  Jehyun Park  ;  Man Ki Ju  ;  Jae Sook Song  ;  Myoung Soo Kim  ;  Soon Il Kim  ;  Yu Seun Kim 
Citation
 PEDIATRIC NEPHROLOGY, Vol.24(4) : 737-745, 2009 
Journal Title
 PEDIATRIC NEPHROLOGY 
ISSN
 0931-041X 
Issue Date
2009
MeSH
Acetylcysteine/pharmacology ; Animals ; Antibodies, Blocking/pharmacology ; Cells, Cultured ; Culture Media, Conditioned/chemistry ; Culture Media, Conditioned/metabolism ; Drug Antagonism ; Enzyme Inhibitors/pharmacology* ; Fibronectins/drug effects* ; Fibronectins/genetics ; Fibronectins/metabolism ; Guanosine/pharmacology ; IMP Dehydrogenase/antagonists & inhibitors* ; IMP Dehydrogenase/genetics ; IMP Dehydrogenase/metabolism ; Mesangial Cells/drug effects* ; Mesangial Cells/metabolism ; Mice ; Mice, Transgenic ; Mycophenolic Acid/pharmacology* ; Oleic Acid/pharmacology* ; RNA Interference/drug effects ; RNA, Small Interfering/pharmacology ; Reactive Oxygen Species/metabolism ; Transforming Growth Factor beta/immunology
Keywords
Mycophenolic acid ; Chronic allograft nephropathy ; Mesangial cell ; Inosine monophosphate dehydrogenase 2 ; Oleic acid ; Hyperlipidemia ; Extracellular matrix ; Reactive oxygen species
Abstract
The synthesis of extracellular matrix (ECM) in mesangial cells (MCs) plays important roles in the development and progression of renal diseases, including chronic allograft nephropathy. Mycophenolic acid (MPA), an inhibitor of inosine monophosphate dehydrogenase 2 (IMPDH2), suppresses MC proliferation and ECM synthesis. However, the exact inhibitory mechanism of MPA on MCs has not been clearly elucidated. In this study we compared the inhibitory effects of MPA and IMPDH2 reduction [by using small interfering RNA (siRNA)] on oleic acid (OA)-induced fibronectin secretion and cellular reactive oxygen species (ROS) in mouse MCs. Growth-arrested MCs were stimulated with OA in the presence or absence of MPA, IMPDH2 siRNA, N-acetylcysteine (NAC), transforming growth factor beta (TGF-beta) antibody or exogenous guanosine. Fibronectin secretion into the medium was examined by Western blot, dichlorodihydrofluorescein (DCF)-sensitive cellular ROS by fluorescence-activated cell scanning (FACS), TGF-beta levels in the media by enzyme-linked immunosorbent assay (ELISA). OA increased fibronectin secretion, TGF-beta and cellular ROS levels. A TGF-beta neutralizing antibody effectively suppressed OA-induced fibronectin secretion. NAC and MPA completely suppressed OA-induced fibronectin secretion and decreased the levels of TGF-beta and cellular ROS. However, IMPDH2 siRNA partly inhibited OA-induced MC activation. Exogenous guanosine successfully reversed the inhibitory effects of IMPDH2 siRNA on OA-induced MC activation. Pleiotropic inhibitory effect of MPA on OA-induced mouse MC activation was mediated via its antioxidant effect on cellular ROS production and partly via inhibition of IMPDH2 itself. Our results implicate ROS as an alternative therapeutic target for the prevention of hyperlipidemia-related glomerulopathy, chronic allograft nephropathy, and subsequent graft loss.
Full Text
http://link.springer.com/article/10.1007%2Fs00467-008-1075-8
DOI
10.1007/s00467-008-1075-8
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Surgery (외과학교실) > 1. Journal Papers
Yonsei Authors
Kim, Soon Il(김순일) ORCID logo https://orcid.org/0000-0002-0783-7538
Kim, Yu Seun(김유선) ORCID logo https://orcid.org/0000-0002-5105-1567
Joo, Man Ki(주만기) ORCID logo https://orcid.org/0000-0002-4112-7003
Huh, Kyu Ha(허규하) ORCID logo https://orcid.org/0000-0003-1364-6989
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/103519
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