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孕酮以剂量依赖方式调节3T3-L1小鼠前脂肪细胞中肝细胞生长因子的产生。

Progesterone dose-dependently modulates hepatocyte growth factor production in 3T3-L1 mouse preadipocytes.

作者信息

Ito Tomoki, Yamaji Daisuke, Kamikawa Akihiro, Abd Eldaim Mabrouk Attia, Okamatsu-Ogura Yuko, Terao Akira, Saito Masayuki, Kimura Kazuhiro

机构信息

Department of Biomedical Sciences, Graduate School of Veterinary Medicine, Hokkaido University, Sapporo 060-0818, Japan.

出版信息

Endocr J. 2017 Aug 30;64(8):777-785. doi: 10.1507/endocrj.EJ17-0097. Epub 2017 Jul 27.

Abstract

It is well documented that estrogen is predominant inducer of hepatocyte growth factor (HGF) in a variety of cell types. However, the effect of progesterone (P) remains to be elusive. Thus, in the present study, we examined the effect of P and combined effect of P and 17β-estradiol (E2) on HGF expression and production in 3T3-L1 fibroblastic preadipocytes and mature adipocytes, as a model of stromal cells. Northern blot analysis showed that hgf mRNA expressed in preadipocytes was notably higher than that of mature adipocytes, and increased by treatment of preadipocytes with E2 or 10 nM P, but not with 1,000 nM P. The E2-induced hgf mRNA expression was enhanced by 10 nM P, but suppressed by 1,000 nM P. Western blot analysis revealed that biological active forms of HGF protein was found in the preadipocyte culture medium, while the lesser amount of HGF precursor protein was detected in the mature adipocyte culture medium. The amounts of HGF were changed dependently on the hgf mRNA expression levels. These results indicate that HGF production is intricately regulated by E2 and P at the transcriptional levels in 3T3-L1 cells, and may explain the changes in the HGF production during the mammary gland development, especially decrease in HGF expression during pregnancy when P concentration is high.

摘要

有充分文献记载,雌激素是多种细胞类型中肝细胞生长因子(HGF)的主要诱导剂。然而,孕酮(P)的作用仍不明确。因此,在本研究中,我们以3T3-L1成纤维前脂肪细胞和成熟脂肪细胞作为基质细胞模型,研究了孕酮以及孕酮与17β-雌二醇(E2)联合作用对HGF表达和产生的影响。Northern印迹分析表明,前脂肪细胞中表达的hgf mRNA明显高于成熟脂肪细胞,用E2或10 nM孕酮处理前脂肪细胞可使其增加,但1000 nM孕酮则无此作用。E2诱导的hgf mRNA表达在10 nM孕酮作用下增强,但在1000 nM孕酮作用下受到抑制。Western印迹分析显示,在前脂肪细胞培养基中发现了生物活性形式的HGF蛋白,而在成熟脂肪细胞培养基中检测到的HGF前体蛋白较少。HGF的量随hgf mRNA表达水平而变化。这些结果表明,在3T3-L1细胞中,E2和P在转录水平上对HGF的产生进行复杂调控,这可能解释了乳腺发育过程中HGF产生的变化,尤其是在孕期孕酮浓度较高时HGF表达的下降。

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