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FOXO3在脑缺血中的作用

The Role of FOXO3 in Cerebral Ischemia
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摘要 脑缺血是导致死亡和长期残疾的主要原因,是一个全球性的健康问题,其病因复杂,发病机制尚不明确。转录因子叉头盒蛋白O3(Forkhead box protein O3, FOXO3)经翻译后修饰(posttranslational modifications, PTMs)后,自身活性发生改变,通过对靶基因的调控,参与调节脑缺血后的凋亡、炎症、氧化应激、自噬及血脑屏障损伤。值得注意的是, FOXO3对缺血性脑损伤不但有促进作用,还具有保护作用。该文就FOXO3的结构及翻译后修饰进行简单介绍,阐述其在脑缺血中的作用,旨在为该疾病的研究提供新思路。 Cerebral ischemia is a major cause of death and long-term disability,which is a global health problem with complex etiology and unclear pathogenesis.The transcriptional factor FOXO3(Forkhead box protein O3)changes its activity after PTMs(post-translation modifications),and it is involved in the regulation of apoptosis,inflammation,oxidative stress,autophagy and blood-brain barrier after cerebral ischemia through the regulations of target genes.It is noteworthy that FOXO3 not only promotes but also protects ischemic brain injury.In this paper,the structure and post-translational modification of FOXO3 are briefly introduced,and its role in cerebral ischemia is expounded,in order to provide new ideas for the study of this disease.
作者 储晓娇 王锦坤 章帆 尚文豆 刘苏亚 何治 CHU Xiaojiao;WANG Jinkun;ZHANG Fan;SHANG Wendou;LIU Suya;HE Zhi(Third Grade Pharmacological Laboratory on Traditional Chinese Medicine,State Administration of Traditional Chinese Medicine,China Three Gorges University,Yichang 443002,China;Basic Medical Science,China Three Gorges University,Yichang 443002,China)
出处 《中国细胞生物学学报》 CAS CSCD 2023年第5期795-801,共7页 Chinese Journal of Cell Biology
基金 湖北省卫健委联合基金重点项目(批准号:WJ2019H526) 天然产物研究与利用湖北省重点实验室开放基金(批准号:NPRD-2018001) 国家自然科学基金(批准号:82073824)资助的课题。
关键词 FOXO3 脑缺血 翻译后修饰 FOXO3 cerebral ischemia post-translational modification
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  • 1罗维.自噬与凋亡的相互作用对视网膜感光细胞死亡途径的影响[J].世界最新医学信息文摘,2019,0(76):109-110. 被引量:2
  • 2Guerit D, Brondello JM, Chuchana P, et al. FOXO3A regulation by miRNA-29a Controls chondrogenic differentiation of mesenchymal stem cells and cartilage formation[J]. Stem Cells Dev, 2014, 23(11): 1195-1205.
  • 3Seiler F, Hellberg J, Lepper PM, et al. FOXO transcription factors regulate innate immune mechanisms in respiratory epithelial cells[J]. J Immunol, 2013, 190(4): 1603-1613.
  • 4Sanchez AM, Candau RB, Bernardi H. FoxO transcription factors: their roles in the maintenance of skeletal muscle homeostasis[J]. Cell Mol Life Sci, 2014, 71(9): 1657-1671.
  • 5Schuff M, Siegel D, Bardine N, et al. FoxO genes are dispensable during gastrulation but required for late embryogenesis in Xenopus laevis[J]. Dev Biol, 2010, 337(2): 259-273.
  • 6Kim J, Choi H, Cho EG, et al. FoxO3a is an antimelanogenic factor that mediates antioxidant-induced depigmentation[J]. J Invest Dermatol, 2014, 134(5): 1378-1388.
  • 7Al-Anati L, Kadekar S, Hogberg J, et al. PCB153, TCDD and estradiol compromise the benzo[a]pyrene-induced p53-response via FoxO3a[J]. Chem Biol Interact, 2014, 219: 159-167.
  • 8Kong W, He L, Coppola M, et al. MicroRNA-155 regulates cell survival, growth, and chemosensitivity by targeting FOXO3a in breast cancer[J]. T J Biol Chem, 2010, 285(23): 17869-17879.
  • 9Senf SM, Sandesara PB, Reed SA, et al. p300 Acetyltransferase activity differentially regulates the localization and activity of the FOXO homologues in skeletal muscle[J]. Am J Physiol Cell Physiol, 2011, 300(6): 1490-1501.
  • 10Xie C, Song LB, Wu JH, et al. Upregulator of cell proliferation predicts poor prognosis in hepatocellular carcinoma and contributes to hepatocarcinogenesis by downregulating FOXO3a[J]. PLoS One, 2012, 7(7): 40607.

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