The transcription factor prolactin regulatory element-binding protein mediates prolactin transcription induced by thyrotropin-releasing hormone in GH3 cells

被引:0
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作者
Xiao Yu
Koji Murao
Hitomi Imachi
Junhua Li
Takamasa Nishiuchi
Hiroaki Dobashi
Naohisa Hosomi
Hisashi Masugata
Guo-Xing Zhang
Hisakazu Iwama
Toshihiko Ishida
机构
[1] Kagawa University,Division of Endocrinology and Metabolism, Department of Internal Medicine, Faculty of Medicine
[2] Soochow University,Laboratory of Cellular and Molecular Tumor Immunology, Medical College
[3] Kagawa University,Department of Cardiorenal and Cerebrovascular Medicine, Faculty of Medicine
[4] Kagawa University,Department of Integrated Medicine, Faculty of Medicine
[5] Nara Medical University,Department of Physiology II
[6] Kagawa University,Life Science Research Center
来源
Endocrine | 2010年 / 38卷
关键词
Prolactin regulatory element-binding protein; Thyrotropin-releasing hormone; Prolactin; Pituitary; Promoter; Transcription;
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学科分类号
摘要
The prolactin regulatory element-binding protein (PREB) is a transcription factor that regulates prolactin (PRL) promoter activity in the rat anterior pituitary. PRL gene expression and secretion are regulated by various hormones and growth factors, including dopamine, epidermal growth factor, and thyrotropin-releasing hormone (TRH). We examined the effect of TRH on PREB expression in pituitary cells. Western blots probed with a PREB-specific antiserum showed that the relative abundance of PREB in GH3 cells increased on treatment with TRH in a dose-dependent manner. The relative abundance of PREB mRNA also increased in a dose-dependent manner after treatment with TRH. TRH induced the expression of the luciferase reporter protein under the PREB promoter control. We used inhibitors of certain signal transduction pathways to show that TRH-induced PREB induction is sensitive to the protein kinase A (PKA) inhibitor. TRH stimulated the activity of the wild-type PRL promoter, whereas mutation of the PREB core-binding element on the PRL promoter reduced this ability. In summary, we have shown that TRH stimulated PREB expression in GH3 cells via the PKA pathway. PREB can function as a transcriptional regulator of PRL promoter activity and might be involved in TRH-induced PRL gene transcription.
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页码:53 / 59
页数:6
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