期刊文献+

FOXO蛋白在动物细胞的分化、增殖、免疫、衰老调节中的作用 被引量:9

FOXO in the regulation of differentiation proliferation immunity and aging of cells
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摘要 目的:总结FOXO亚家族在动物细胞的分化、生长、增殖、代谢、免疫及衰老调节方面的多样性功能,为进一步开展FOXO研究提供新思路。资料来源:应用计算机检索Medline2000-01/2005-05关于FOXO的文章。检索词“foxo”,文章的语种类采用系统默认值。同时利用计算机检索中国期刊全文数据库2000-01/2004-05相关的文章,限定文章语言种类为中文,检索词“foxo”或“forkhead转录因子”。资料选择:收集到119篇文献,对资料进行初审,排除重复性研究,选择重点研究FOXO蛋白在动物细胞的分化、增殖、免疫、衰老等调节功能方面作用的相关文献47篇,其中研究相似的以发表在较权威杂志者优先。资料提炼:将筛选到的47篇文献按照FOXO蛋白在动物细胞的分化、增殖、免疫、衰老等调节功能方面的作用分类。其中有11篇主要关于FOXO信号转导方面的文献,9篇与细胞的分化和增殖有关,5篇与生长发育有关,13篇与代谢明显有关,6篇与免疫有关,5篇与繁殖有关,9篇与衰老调节有关。资料综合:47篇文献共涉及到了从线虫、果蝇低等低等动物到哺乳动物(小鼠、大鼠与人)等多种动物或细胞的有关FOXO亚家族在细胞的分化、生长、增殖、代谢、免疫及衰老调节方面的调节功能。结论:FOXO是Fox蛋白亚家族的成员之一,其位于很多信号转导途径的交叉点,在动物细胞的分化、生长、增殖、代谢、免疫及衰老调节方面具有重要的多样性功能。 OBJECTIVE: To sumup the various functions of FOXO subfamily involvingin the cellular differentiation growth proliferation metabolism, immunity and aging of the animals so as to provide new way for further developing study on FOXO. DATA SOURCES: We computer-searched Medline database for the related articles published from January 2000 to May 2005 on FOXO proteins, with the key word of "foxo", The language was default. Meanwhile, we also computer- searched the China Journal Full-text Database for related articles published from January 2000 to May 2004 with the key words of "foxo" or "Forkhead transcription factor", and the language was limited to Chinese. STUDY SELECTION: We screened primarily 119 literatures about FOXO, The repeated researches were excluded. 47 articles about FOXO involving in the cellular differentiation proliferation, and immunity and aging were selected. If the study contents were similar, the more authoritative ones were selected. DATA EXTRACTION: The screened 47 articles were classified according to the function of FOXOs involving in the cellular differentiation, proliferation, immunity and aging and so on In the 47 literatures selected, 11 of them were mainly related to signal transduction of FOXO, 9 were related to the cellular differentiation and proliferation, 5 were related to the animal development and growth, 13 were obviously related to cellular metabolism, 6 were related to immunity, 5 were related to reproduction, and 9 were related to aging. DATA SYNTHESIS: The 47 literatures which almost included the experimental results about Caenorhabditis elegans, fruit fly, mice. rat and human with their cells showed that FOXO can regulate the cellular differentiation, growth, proliferation, metabolism, immunity, aging and so on. ' CONCLUSION: The FOXO proteins, one of the subfamilies of Forkhead transcription factors, are at the crossroads of many cellular signaling pathways and have important various functions in cellular differentiation, growth. proliferation, metabolism, immunity, aging and so on of the animals.
出处 《中国临床康复》 CSCD 北大核心 2006年第9期158-162,共5页 Chinese Journal of Clinical Rehabilitation
基金 国家自然科学基金资助(30571335)~~
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参考文献47

  • 1Foulstone E,Prince S,Zaccheo O,et al.Insulin-like growth factor ligands,receptors,and binding proteins in cancer.J Pathol 2005,205(2):145-53。
  • 2Brenkman AB,Burgering BM.FoxO3a eggs on fertility and aging.Trends Mol Med 2003 ,9(11):464-7.
  • 3Burgering BM,Kops GJ.Cell cycle and death control:long live Forkheads.Trends Biochem Sci 2002,27(7):352-60.
  • 4Castrillon DH,Miao L,Kollipara R,et al.Suppression of ovarian follicle activation in mice by the transcription factor Foxo3a.Science 2003 ,301(5630):215-8.
  • 5Hu MC,Lee DF,Xia W,et al.IκB kinase promotes tumorigenesis through inhibition of forkhead Foxo3a.Cell 2004,117(2):225-37.
  • 6Seoane J,Le HV,Shen L,et al.Integration of smad and forkhead pathways in the control of neuroepothelial and glioblastoma cell proliferation.Cell 2004, 117(2):211-23.
  • 7Huang H,Regan KM,Wang F,et al.Skp2 inhibits Foxol in tumor suppression through ubiquitin-mediated degradation.Proc Natl Acad Sci USA 2005, 102(5):1649-54.
  • 8Kino T,De Martino MU,Charmandari E,et al.HIV-1 accessory protein Vpr inhibits the effect of insulin on the Foxo subfamily of forkhead transcription factors by interfering with their binding to 14-3-3 proteins:potential clinical implications regarding the insulin resistance of HIV-1-infected patients.Diabetes 2005 ,54(1):23-31.
  • 9Yang H,Zhao R,Yang HY,et al.Constitutively active FoxO4 inhibits Akt activity,regulates p27Kip1 stability,and suppresses HER2-mediated tumorigenicity.Oncogene 2005,24(11):1924-35.
  • 10van der Heide LP,Smidt MP.Regulation of FoxO activity by CBP/p300-mediated acetylation.Trends Biochem Sci 2005,30(2):81-6.

同被引文献167

  • 1闫梦晗,李晓.升陷汤加味治疗慢性心力衰竭气虚血瘀水饮内停证的临床观察[J].世界最新医学信息文摘,2019,0(86):104-105. 被引量:7
  • 2林芳,顾振纶,秦正红.自噬及其在细胞代谢和疾病中的作用[J].生物化学与生物物理进展,2005,32(4):298-303. 被引量:22
  • 3李学斌,谢庄,石放雄.FOXO蛋白的修饰与细胞凋亡和癌变[J].生物化学与生物物理进展,2005,32(7):600-606. 被引量:6
  • 4赵文惠,萧建中,杨文英,王娜,王昕,陈晓平,卜石.肝脏胰岛素抵抗与肝糖输出调控基因表达的关系[J].中华肝脏病杂志,2006,14(1):45-48. 被引量:27
  • 5Mittelman SD, Van Citters GW, Kirkman EL, et al. Extreme insulin resistance of the central adipose depot in vivo. Diabetes, 2002, 51: 755-761.
  • 6Kabir M, Catalano K J, Ananthnarayan S, et al Molecular evidence supporting the portal theory: a causative link between visceral adiposity and hepatic insulin rcsistance. Am J Physioi Endocrinoi Metab, 2005, 288: E454-461.
  • 7Barzilai N, Banerjee S, Hawkins M, et al. Caloric restriction reverses hepatic insulin resistance in aging rats by decreasing visceral fat. J Ciin Invest, 1998, 101: 1353-1361.
  • 8Nakae J, Biggs WH 3rd, Kitamura T, et ai. Regulation of insulin action and pancreatic beta-cell function by mutated alleles of the gene encoding forkhead transcription factor Foxol. Nat Genet, 2002, 32: 245-253.
  • 9Aitomonte J, Richter A, Harbaran S, et al. Inhibition of Foxol function is associated with improved fasting glycemia in diabetic mice. Am J Physioi Endocrinol Metab, 2003, 285: E718-728.
  • 10Park SY, Choi GH, Choi HI, et al. Calorie restriction improves wholebody glucose disposal and insulin resistance in association with the increased adipoeyte-speeifie GLUT4 expression in Otsuka Long- Evans Tokushima fatty rats. Arch Biochem Biophys, 2005, 436: 276- 284.

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