期刊文献+

AMPK与脂肪细胞分化的关系研究及其在人脂肪源性肿瘤组织中的表达特点 被引量:2

The Role of AMPK in the Differentiation of Human Adipocyte and the Expressing Features in Human Lipoma or Liposarcoma
原文传递
导出
摘要 目的:探讨AMPK在脂肪细胞分化过程中的作用以及与脂滴相关表面蛋白Cidec的表达关系,为肥胖发生及其防治肥胖及肥胖相关性疾病提供重要的理论依据。方法:通过免疫组织化学、Real-time PCR和Western blot等方法分析AMPK和Cidec在脂肪细胞分化中的作用,明确二者的相关性。结果:在不同分化程度的脂肪源性肿瘤组织中,AMPK表达随着脂肪细胞分化程度的升高而表达降低,而Cidec的表达是逐渐增高的;在不同发育阶段的胎儿脂肪组织中,AMPK随着胎龄的增加表达逐渐降低(P<0.01),而Cidec的表达则呈逐渐增高的趋势(P<0.01);以上AMPKα的表达均与Cidec的表达水平呈负相关。结论:AMPK可能在脂肪细胞分化过程中扮演重要角色,研究其与Cidec的表达与作用关系可能为脂肪细胞发育及分化提供重要线索及依据。 Objective:In this study,we would emphatically study the role of AMPK in the process of adipocyte differentiation and dig out its possible relationship with Cidec during adipogenesis,in order to provide a potential role for AMPKα as a target in treating obesity or obesity-related diseases.Methods:Using IHC staining,real-time polymerase chain reaction (RT-PCR) and western blot analysis to detect AMPK and Cidec expression in different differentiation phase of human adipocytic tumors,as well as different developmental stages of human fetal adipose tissue.Results:The results showed that AMPK was gradually increased with a decrease in differentiation of the tumor cells,while Cidec was gradually decreased;and in the fetal adipose tissues,AMPK decreased (P〈0.01) and Cidec increased (P〈0.01) significantly with the birth age increased.It was implied that AMPK was closely related with adipocytes differentiation,and showed a reverse trend compared with Cidec during the differentiation course of human adipocytes.Conclusion:In this study,we demonstrated that AMPK played a key role during the differentiation of adipocytes,thus might propose important clues to discover new possible mechanism for human adipogenesis.
出处 《现代生物医学进展》 CAS 2017年第15期2833-2836,2852,共5页 Progress in Modern Biomedicine
基金 国家自然科学基金项目(31400722)
关键词 肥胖 脂肪细胞 AMPK 分化 Cidec Adiposity Adipocyte AMPK Differentiation Cidec
  • 相关文献

参考文献1

二级参考文献14

  • 1Inohara N, Koseki T, Chen S, et al. CIDE, a novel family of cell death activators with homology to the 45 kDa subunit of the DNA fragmentation factor[ J ]. EMBO J, 1998,7 (9) :2526 - 2533.
  • 2Liang L, Zhao M, Xu Z, et al. Molecular cloning and characterization of CIDE - 3 a novel member of the cell - death - inducing DNA - fragmentation - factor ( DFF45 ) - like effector family [ J ]. Biochem J ,2003,370 ( 1 ) : 195 - 203.
  • 3Skubitz KM, Cheng EY, Clohisy DR, et al. Differential gene expression in liposarcoma, lipoma, and adipose tissue [ J ]. Cancer Invest,2005,23 (2) : 105 - 118.
  • 4Danesch U, Hoeck W, Ringold GM. Cloning and transcriptional regulation of a novel adipocyte- specific gene, FSP27. CAAT- enhancer - binding protein (C/EBP) and C/EBP - like proteins interact with sequences required for differentiation - dependent ex- pression[ J]. J Biol Chem,1992,267(10) :7185 -7193.
  • 5Mack TM. Sarcomas and other malignancies of soft tissue, retroperitoneum,peritoneum, pleura, heart, mediastinum, and spleen [ J]. Cancer, 1995,75 ( 1 Suppl) :211 - 244.
  • 6Mentzel T, Fletcher CD. Lipomatous tumours of soft tissues: an update[J]. Virchows Arch,1995,427 (4) :353 -363.
  • 7Weiss SW G. Liposarcoma. Enzinger and Weiss's soft tissue tumors[ M]. 2001: 4th ed,St Louis :Mosby, 641 -694.
  • 8Chang HR, Hajdu SI, Collin C, et al. The prognostic value of histologic subtypes in primary extremity liposarcoma [ J ]. Cancer, 1989,64 (7) :1514 - 1520.
  • 9Nijhuis PH, Sars PR, Plaat BE, et al. Clinico - pathological data and prognostic factors in completely reseeted AJCC stage Ⅰ -Ⅲ liposareomas[J]. Ann Surg Oneol, 2000,7(7) :535 -543.
  • 10Tontonoz P, Singer S, Forman BM, et al, Terminal differentiation of human liposarcoma cells induced by ligands for peroxisome proliferator-activated receptor gamma and the retinoid Ⅹ receptor [J]. Proc Nail Acad Sci USA,1997, 94(1) : 237 -241.

同被引文献15

引证文献2

二级引证文献4

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部