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非侵入性基因治疗在中枢神经系统疾病中的应用 被引量:1

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摘要 非侵入性地将具有治疗作用的基因通过血脑屏障输送至脑内,以治疗中枢神经系统疾病,是生物学领域研究的难点和热点,而应用适宜的转运载体是解决这一难题的有效途径。使用病毒载体或非病毒载体,已成功进行非侵入性基因治疗的中枢神经系统疾病有实验性运动神经疾病、脑部肿瘤和帕金森病等。随着对脑微血管内皮细胞上的受体的研究和新型载体的开发,应用非侵入性基因治疗中枢神经系统疾病将会更为广泛。
出处 《生理科学进展》 CAS CSCD 北大核心 2010年第4期307-309,共3页 Progress in Physiological Sciences
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参考文献10

  • 1Pardridge WM.Blood-brain barrier delivery of protein and non-viral gene therapeutics with molecular Trojan horses.J Control Release,2007,122:345-348.
  • 2Foust KD,Nurre E,Montgomery CL,et al.Intravascular AAV9 preferentially targets neonatal neurons and adult astrocytes.Nat Biotechnol,2009,27:59-65.
  • 3Ko YT,Bhattacharya R,Bickel U.Liposome encapsulated polyethylenimine/ODN polyplexes for brain targeting.J Control Release,2009,133:230-237.
  • 4Boado RJ.Blood-brain barrier transport of non-viral gene and RNAi therapeutics.Pharm Res,2007,24:1772-1787.
  • 5Zhang Y,Schlachetzki F,Zhang YF,et al.Normalization of striatal tyrosine hydroxylase and reversal of motor impairment in experimental Parkinsonism with intravenous nonviral gene therapy and a brain-specific promoter.Hum Gene Ther,2004,15:339-350.
  • 6Huang R,Ke W,Liu Y,et al.The use of lactoferrin as a ligand for targeting the polyamidoamine-based gene delivery system to the brain.Biomaterials,2008,29:238-246.
  • 7Xia CF,Zhang Y,Zhang Y,et al.Intravenous siRNA of brain cancer with receptor targeting and avidin-biotin technology.Pharm Res,2007,24:2309-2316.
  • 8Vinogradov SV,Batrakova EV,Kabanov AV.Nanogels for oligonucleotide delivery to the brain.Bioconjug Chem,2004,15:50-60.
  • 9Kumar P,Wu H,McBride JL,et al.Transvascular delivery of small interfering RNA to the central nervous system.Nature,2007,448:39-43.
  • 10Miana-Mena FJ,Muoz MJ,Roux S,et al.A Non-viral vector for targeting gene therapy to motoneurons in the CNS.Neurodegenerative Dis,2004,1:101-108.

同被引文献21

  • 1Brasseur R,Divita G. Happy birthday cell penetrating peptides:already 20 years[J].Biochimica Et Biophysica Acta,2010,(12):2177-2181.
  • 2Frankel AD,Pabo CO. Cellular uptake of the tat protein from human immunodeficiency virus[J].Cell,1988,(06):1189-1193.doi:10.1016/0092-8674(88)90263-2.
  • 3Joliot A,Pernelle C,Deagostini-Bazin H. Antennapedia homeobox peptide regulates neural morphogenesis[J].Proceedings of the National Academy of Sciences(USA),1991,(05):1864-1868.
  • 4Vivès E,Brodin P,Lebleu B. A truncated HIV-1 Tat protein basic domain rapidly translocates through the plasma membrane and accumulates in the cell nucleus[J].Journal of Biological Chemistry,1997,(25):16010-16017.
  • 5Morris MC,Vidal P,Chaloin L. A new peptide vector for efficient delivery of oligonucleotides into mammalian cells[J].Nucleic Acids Research,1997,(14):2730-2736.
  • 6Schwarze SR,Ho A,Vocero-Akbani A. In vivo protein transduction:delivery of a biologically active protein into the mouse[J].Science,1999,(5433):1569-1572.doi:10.1126/science.285.5433.1569.
  • 7Xiang L,Zhou R,Fu A. Targeted delivery of large fusion protein into hippocampal neurons by systemic administration[J].Journal of Drug Targeting,2011,(08):632-636.
  • 8Lindgren M,Langel U. Classes and prediction of cell-penetrating peptides[J].Methods in Molecular Biology,2011.3-19.
  • 9Pooga M,Langel U. Synthesis of cell-penetrating peptides for cargo delivery[J].Methods in Molecular Biology,2005.77-89.
  • 10Toivonen JM,Oliván S,Osta R. Tetanus toxin C-fragment:the courier and the cure[J].Toxicology,2010,(11):2622-2644.

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