Proliferating effects of the flavonoids daidzein and quercetin on cultured chicken primordial germ cells through antioxidant action

被引:32
作者
Tang, Xinyan [1 ]
Zhang, Caiqiao [1 ]
Zeng, Weidong [1 ]
Mi, Yuling [1 ]
Liu, Hongyun [1 ]
机构
[1] Zhejiang Univ, Dept Vet Med, Coll Anim Sci, Hangzhou 310029, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
antioxidant; chicken; daidzein; flavonoids; primordial germ cell; proliferation; protein kinase A; quercetin;
D O I
10.1016/j.cellbi.2006.02.004
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Primordial germ cells (PGCs) are undifferentiated pluripotent stem cells, whose proliferation is influenced by many internal and external factors. In the present study, a PGC-somatic cell co-culture model was established to evaluate effects of the flavonoids daidzein (DAI) and quercetin (QUE) on proliferation of PGCs from embryonic chickens. PGCs were isolated from the germinal ridge of 3.5-4 day embryos and cultured in 5% fetal calf serum (FCS)-supplemented Medium 199. PGC subculture was carried out on chicken embryonic fibroblast feeder (CEF) or follicular granulosa cell feeder (GCF) layers. The subcultured PGCs were challenged with flavonoids alone or in combination with a reactive oxygen substance (ROS)-producing system on CEF for 48 h. The results showed a better supporting effect of CEF than GCF. Flavonoids (1 mu g/ ml) significantly promoted PGC proliferation, which could be markedly inhibited by ROS. The oxidative damage by ROS was further manifest by decreased superoxide dismutase activity and glutathione levels. In addition, activation of protein kinase A (PKA) by forskolin significantly stimulated PGC proliferation, but PKA inhibitor H89 inhibited the proliferating effects induced by DAI and QUE. These results indicated that cultured PGCs respond to exogenous agents on proliferation and that antioxidant flavonoids could restore the intracellular antioxidant system and promote PGC proliferation via their antioxidant action involving the PKA signaling pathway. (c) 2006 International Federation for Cell Biology. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:445 / 451
页数:7
相关论文
共 33 条
[21]   LONG-TERM PROLIFERATION OF MOUSE PRIMORDIAL GERM-CELLS IN CULTURE [J].
RESNICK, JL ;
BIXLER, LS ;
CHENG, LZ ;
DONOVAN, PJ .
NATURE, 1992, 359 (6395) :550-551
[22]   Depolarization-dependent effect of flavonoids in rat uterine smooth muscle contraction elicited by CaCl2 [J].
Revuelta, MP ;
Cantabrana, B ;
Hidalgo, A .
GENERAL PHARMACOLOGY-THE VASCULAR SYSTEM, 1997, 29 (05) :847-857
[23]   Biotransformation of soy isoflavone-glyco sides in laying hens: intestinal absorption and preferential accumulation into egg yolk of equol, a more estrogenic metabolite of daidzein [J].
Saitoh, S ;
Sato, T ;
Harada, H ;
Matsuda, T .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2004, 1674 (02) :122-130
[24]   Oxidative stress in carcinogenesis.: Correlation between lipid peroxidation and induction of preneoplastic lesions in rat hepatocarcinogenesis [J].
Sánchez-Pérez, Y ;
Carrasco-Legleu, C ;
García-Cuellar, C ;
Pérez-Carreón, J ;
Hernández-García, S ;
Salcido-Neyoy, M ;
Alemán-Lazarini, L ;
Villa-Treviño, S .
CANCER LETTERS, 2005, 217 (01) :25-32
[25]   MAPK signaling in neurodegeneration: influences of flavonoids and of nitric oxide [J].
Schroeter, H ;
Boyd, C ;
Spencer, JPE ;
Williams, RJ ;
Cadenas, E ;
Rice-Evans, C .
NEUROBIOLOGY OF AGING, 2002, 23 (05) :861-880
[26]   In vitro survival and proliferation of porcine primordial germ cells [J].
Shim, H ;
Anderson, GB .
THERIOGENOLOGY, 1998, 49 (03) :521-528
[27]   Cellular uptake and metabolism of flavonoids and their metabolites: implications for their bioactivity [J].
Spencer, JPE ;
El Mohsen, MMA ;
Rice-Evans, C .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2004, 423 (01) :148-161
[28]   STUDY ON DIVISION OF PRIMORDIAL GERM-CELLS IN EARLY CHICK-EMBRYO [J].
SWARTZ, WJ ;
DOMM, LV .
AMERICAN JOURNAL OF ANATOMY, 1972, 135 (01) :51-+
[29]   Soy isoflavones improve endothelial function in spontaneously hypertensive rats in an estrogen-independent manner:: Role of nitric-oxide synthase, superoxide, and cyclooxygenase metabolites [J].
Vera, R ;
Galisteo, M ;
Villar, IC ;
Sánchez, M ;
Zarzuelo, A ;
Pérez-Vizcaino, F ;
Duarte, J .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2005, 314 (03) :1300-1309
[30]   Proliferative feeder cells support prolonged expansion of human embryonic stem cells [J].
Xie, CQ ;
Lin, G ;
Yuan, D ;
Wang, J ;
Liu, TC ;
Lu, GX .
CELL BIOLOGY INTERNATIONAL, 2005, 29 (08) :623-628