Circadian Clock genes Per2 and clock regulate steroid production, cell proliferation, and luteinizing hormone receptor transcription in ovarian granulosa cells

被引:52
作者
Shimizu, Takashi [1 ]
Hirai, Yuko [1 ]
Murayama, Chiaki [1 ]
Miyamoto, Akio [1 ]
Miyazaki, Hitoshi [2 ]
Miyazaki, Koyomi [3 ]
机构
[1] Obihiro Univ Agr & Vet Med, Grad Sch Anim & Food Hyg, Obihiro, Hokkaido 0808555, Japan
[2] Univ Tsukuba, Ctr Gene Res, Tsukuba, Ibaraki 3058572, Japan
[3] Natl Inst Adv Ind Sci & Technol, Biomed Res Inst, Tsukuba, Ibaraki 3058566, Japan
基金
日本学术振兴会;
关键词
Circadian Clock; Steroid hormone; Granulosa cell; Ovary; TUMOR SUPPRESSION; EXPRESSION;
D O I
10.1016/j.bbrc.2011.07.058
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Circadian Clock genes are associated with the estrous cycle in female animals. Treatment with Per2 and Clock siRNAs decreased the number of granulosa cells and LHr expression in follicle-stimulating hormone FSH-treated granulosa cells. Per2 siRNA treatment did not stimulate the production of estradiol and expression of P450arom, whereas Clock siRNA treatment inhibited the production of estradiol and expression of P450arom mRNA. Per2 and Clock siRNA treatment increased and unchanged, respectively, progesterone production in FSH-treated granulosa cells. Similarly, expression of SEAR mRNA was increased by Per2 siRNA and unchanged by Clock siRNA. Our data provide a new insight that Per2 and Clock have different action on ovarian granulosa cell functions. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:132 / 135
页数:4
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