...
首页> 外文期刊>Life sciences >Adipose tissue gene expression profiles in ob/ob mice treated with leptin.
【24h】

Adipose tissue gene expression profiles in ob/ob mice treated with leptin.

机译:瘦素治疗的ob / ob小鼠的脂肪组织基因表达谱。

获取原文
获取原文并翻译 | 示例

摘要

Leptin plays a critical role in regulating body weight, lipid metabolism, apoptosis and microvasculature of adipose tissue. To explore multiple signaling pathways of leptin action on adipose tissue, real-time PCR utilizing TaqMan low-density arrays was performed to compare mRNA expression in adipose tissue of ob/ob mice treated with vehicle or leptin (2.5 microg/d or 10 microg/d) for 14 days via subcutaneous osmotic minipumps. Of the 24 target genes selected for characterization, many were differentially expressed between control ob/ob mice and leptin-treated ob/ob mice. Increases in mRNA expression were found for hormone sensitive lipase (HSL), uncoupling protein 2 (UCP2), adrenergic receptor 3 (ADR3), mitofusin 2 (Mfn2), sirtuin 3 (Sirt3), transcription factor sterol regulatory element binding factor 1 (SREBF1), Bcl-2, Bax, Caspase 3, tumor necrosis factor alpha (TNFalpha), adiponectin and angiopoietin 2 (Ang-2). Decreases in expression were found for stearoyl-coenzyme A desaturase 1 (SCD1), fatty acid synthase (FAS), and retinol binding protein 4 (RBP4). There were no changes in expression of transcription factors involved in adipocyte differentiation (C/EBPalpha, PPARalpha, and PPARgamma). These results confirm that alterations in the expression of specific adipose tissue genes including those associated with the promotion of lipid mobilization, energy dissipation, and apoptosis may mediate leptin-induced fat loss in ob/ob mice.
机译:瘦素在调节脂肪组织的体重,脂质代谢,细胞凋亡和微脉管系统中起关键作用。为了探索瘦素作用于脂肪组织的多种信号传导途径,利用TaqMan低密度阵列进行了实时PCR,比较了接受媒介物或瘦素(2.5 microg / d或10 microg / d的ob / ob小鼠的脂肪组织中的mRNA表达)。 d)通过皮下渗透微型泵持续14天。在选择用于表征的24个靶基因中,许多在对照ob / ob小鼠和瘦素处理的ob / ob小鼠之间差异表达。发现激素敏感性脂肪酶(HSL),解偶联蛋白2(UCP2),肾上腺素能受体3(ADR3),mitofusin 2(Mfn2),sirtuin 3(Sirt3),转录因子固醇调节元件结合因子1(SREBF1)mRNA表达增加),Bcl-2,Bax,Caspase 3,肿瘤坏死因子α(TNFalpha),脂联素和血管生成素2(Ang-2)。发现降低了硬脂酰辅酶A去饱和酶1(SCD1),脂肪酸合酶(FAS)和视黄醇结合蛋白4(RBP4)的表达。参与脂肪细胞分化的转录因子(C / EBPalpha,PPARalpha和PPARgamma)的表达没有变化。这些结果证实,特定脂肪组织基因表达的改变(包括与脂质动员,能量耗散和细胞凋亡的促进有关的那些)可能介导瘦素诱导的ob / ob小鼠脂肪减少。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号