Genipin suppresses subconjunctival fibroblast migration, proliferation and myofibroblast transdifferentiation

被引:30
作者
Kitano, Ai
Saika, Shizuya
Yamanaka, Osamu
Ikeda, Kazuo
Reinach, Peter S.
Nakajima, Yuji
Okada, Yuka
Shirai, Kumi
Ohnishi, Yoshitaka
机构
[1] Wakayama Med Univ, Dept Ophthalmol, Wakayama 6410012, Japan
[2] Osaka Univ, Grad Sch Med, Dept Anat, Suita, Osaka 565, Japan
[3] SUNY Coll Optometry, New York, NY 10010 USA
关键词
genipin; subconjunctival fibroblast; myofibroblast; fibrosis; transforming growth factor-beta;
D O I
10.1159/000096231
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose: Inchin-ko-to is a herbal medicine which has therapeutic effects in ameliorating liver fibrosis or cholestatic liver diseases. Its main bioactive component is genipin, which is an intestinal bacterial metabolite of this medication. Accordingly, we determined whether or not Inchin-ko-to suppresses in a wound healing model subconjunctival fibroblast (SCF) migration proliferation and myofibroblast transdifferentiation since an inhibitory effect could be of value in improving trabeculotomy outcome. Methods: Effects of genipin on SCF cell migration were examined subsequent to wounding confluent monolayer cultures. Alamar blue staining evaluated the effects of genipin (0-50 mu g/ml) on fibroblast cell proliferation. Immunostaining determined alpha-smooth muscle actin (alpha SMA) expression. Western blotting evaluated (alpha SMA) expression and phospho-Smad2 formation. Real-time RT-PCR evaluated TGF beta 1 and collagen I alpha 2 mRNA expression. Enzyme-immunoassay determined culture medium collagen I content. Results: Genipin suppressed wound-induced cell migration and proliferation. It also decreased collagen type I TGF beta 1 and alpha SMA mRNA and protein expression. Smad2 signaling was inhibited by genipin in a dose-dependent manner. Conclusion: Genipin suppresses injury-induced fibrogenic responses in SCFs. This result suggests that the herbal medicine Inchin-ko-to might have therapeutic value following trabeculotomy. Copyright (c) 2006 S. Karger AG, Basel.
引用
收藏
页码:355 / 360
页数:6
相关论文
共 31 条
[1]   A case of severe acute hepatitis of unknown etiology treated with the Chinese herbal medicine Inchinko-to [J].
Arai, M ;
Yokosuka, O ;
Fukai, K ;
Kanda, T ;
Kojima, H ;
Kawai, S ;
Imazeki, F ;
Hirasawa, H ;
Saisho, H .
HEPATOLOGY RESEARCH, 2004, 28 (03) :161-165
[2]   CORRELATION OF FIBROSIS AND TRANSFORMING GROWTH FACTOR-BETA TYPE-2 LEVELS IN THE EYE [J].
CONNOR, TB ;
ROBERTS, AB ;
SPORN, MB ;
DANIELPOUR, D ;
DART, LL ;
MICHELS, RG ;
DEBUSTROS, S ;
ENGER, C ;
KATO, H ;
LANSING, M ;
HAYASHI, H ;
GLASER, BM .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 83 (05) :1661-1666
[3]   Novel antisense oligonucleotides targeting TGF-β inhibit in vivo scarring and improve surgical outcome [J].
Cordeiro, MF ;
Mead, A ;
Ali, RR ;
Alexander, RA ;
Murray, S ;
Chen, C ;
York-Defalco, C ;
Dean, NM ;
Schultz, GS ;
Khaw, PT .
GENE THERAPY, 2003, 10 (01) :59-71
[4]  
Cordeiro MF, 2000, INVEST OPHTH VIS SCI, V41, P756
[5]  
Cordeiro MF, 1999, INVEST OPHTH VIS SCI, V40, P1975
[6]   Mediation of transforming growth factor-β1-stimulated matrix contraction by fibroblasts -: A role for connective tissue growth factor in contractile scarring [J].
Daniels, JT ;
Schultz, GS ;
Blalock, TD ;
Garrett, Q ;
Grotendorst, GR ;
Dean, NM ;
Khaw, PT .
AMERICAN JOURNAL OF PATHOLOGY, 2003, 163 (05) :2043-2052
[7]   Tissue repair, contraction, and the myofibroblast [J].
Desmoulière, A ;
Chaponnier, C ;
Gabbiani, G .
WOUND REPAIR AND REGENERATION, 2005, 13 (01) :7-12
[8]   Conjunctival fibrosis in ocular cicatricial pemphigoid - the role of cytokines [J].
Elder, MJ ;
Dart, JKG ;
Lightman, S .
EXPERIMENTAL EYE RESEARCH, 1997, 65 (02) :165-176
[9]   TGF-β1-mediated fibroblast-myofibroblast terminal differentiation -: the role of Smad proteins [J].
Evans, RA ;
Tian, YC ;
Steadman, R ;
Phillips, AO .
EXPERIMENTAL CELL RESEARCH, 2003, 282 (02) :90-100
[10]   Comparison of alamar blue and MTT assays for high through-put screening [J].
Hamid, R ;
Rotshteyn, Y ;
Rabadi, L ;
Parikh, R ;
Bullock, P .
TOXICOLOGY IN VITRO, 2004, 18 (05) :703-710