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细胞对纳米材料的胞吞及其胞内定位相关机制的研究进展 被引量:1

Advances in the Researches on Endocytosis and Cellular Localization of Nanomaterials and Associated Mechanisms
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摘要 纳米材料具有独特的理化性质,其在纳米生物医药技术中得到广泛的研究,有着良好的应用前景。纳米材料的尺寸分布在纳米级,使其入胞途径和转运方式与一般尺寸的物质略有不同。细胞可通过网格蛋白介导胞吞、陷窝小泡介导胞吞、吞噬作用和巨胞饮等胞吞方式摄取纳米颗粒。吞噬的方式及后续的转运和定位受细胞的类型、状态,以及纳米颗粒的理化性质如元素组成、尺寸、形状、电荷、表面修饰等多种因素共同影响。 In recent years, with the rapid development of nanoscience and nanotechnology, the pharmacological activity and potential value of clinic application have been attracting more and more people to explore the mechanism of the interaction between cells and nanopaticles. The current researches have uncovered that nanoparticles and bulk materials are uptaken by cells in different ways including clathrin-mediated endocytosis, caveolae-mediated endocytosis, phagocytosis and macropinocytosis, which are highly dependent on cell-types and physicochemical properties of particles such as size, charge, elemental composition, surface area and surface chemistry. This review will focus on the advances of the researches on the mechenism of endocytosis and cellular localization of nanoparticles.
出处 《中国细胞生物学学报》 CAS CSCD 北大核心 2013年第12期1826-1831,共6页 Chinese Journal of Cell Biology
基金 上海市科委基础研究重点项目(批准号:13JC1401402) 上海市教委科研创新项目(批准号:14ZZ078) 第二军医大学大学生创新能力培养计划(批准号:ZD2012028 MS2012025)资助的课题~~
关键词 纳米材料 摄眠胞吞 胞内定位 靶向 nanomaterials uptake endocytosis cellular localization target
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  • 1张源,齐宪荣,高燕,魏来.谷甾醇葡萄糖苷和卞泽双重修饰肝实质细胞靶向阳性脂质体介导的基因转染和抗乙肝病毒作用[J].药学学报,2006,41(11):1111-1115. 被引量:4
  • 2Wunderbaldinger P, Josephson L, Weissleder R. Tat peptide directs enhanced clearance and hepatic permeability of magnetic nanoparticles [J]. Bioconjug Chem, 2002, 13: 264-268.
  • 3Marty C, Meylan C, Schott H, et al. Enhanced heparan sulfate proteoglycan-mediated uptake of cell-penetrating peptidemodified liposomes [J]. Cell Mol Life Sci, 2004, 61: 1785- 1794.
  • 4Sethuraman VA, Bae YH. TAT peptide-based micelle system for potential active targeting of anti-cancer agents to acidic solid tumors [J]. J Control Release, 2007, 118: 216-224.
  • 5Juliano RL. Intracellular delivery of oligonucleotide conjugates and dendrimer complexes [J]. Ann NY Acad Sci, 2006, 1082: 18-26.
  • 6Huang YZ, Gao JQ, Chen JL, et al. Cationic liposomes modified with non-ionic surfactants as effective non-viral carrier for gene transfer [J]. Colloids Surf B Biointerfaces, 2006, 49: 158-164.
  • 7Kurtoglu YE, Navath RS, Wang B, et al. Poly(amidoamine) dendrimer-drug conjugates with disulfide linkages for intracellular drug delivery [J]. Biomaterials, 2009, 30: 2112- 2121.
  • 8Tu Y, Kim JS. A fusogenic segment of glycoprotein H from herpes simplex virus enhances transfection efficiency of cationic liposomes [J]. J Gene Med, 2008, 10: 646-654.
  • 9Burckbuchler V, Wintgens V, Leborgne C, et al. Development and characterization of new cyclodextrin polymer-based DNA delivery systems [J]. Bioconjug Chem, 2008, 19: 2311-2320.
  • 10Min SH, Lee DC, Lim MJ, et al. A composite gene delivery system consisting of polyethylenimine and an amphipathic peptide KALA [J]. J Gene Med, 2006, 8: 1425-1434.

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