Centre de Biophysique Moléculaire CNRS UPR, University of Orléans and Inserm, France.
J Drug Target. 2011 Jun;19(5):315-25. doi: 10.3109/1061186X.2010.504262. Epub 2010 Jul 23.
We report for the first time preparation of mannosylated and histidylated lipopolyplexes (Man-LPD100) with uptake and transfection selectivity for dendritic cells (DCs). Man-LPD100 were prepared by addition of mannosylated and histidylated liposomes (Man-Lip100) on preformed PEGylated histidylated polylysine/DNA polyplexes. Man-Lip100 comprised a cationic [O,O-dioleyl-N-(3N-(N-methylimidazolium iodide)propylene) phosphoramidate)] lipid, a neutral [O,O-dioleyl-N-histamine Phosphoramidate] co-lipid and β-D-mannopyranosyl-N-dodecylhexadecanamide (Man-lipid). At the best, Man-Lip100 containing 11 mol % Man-lipid was obtained. We found that dialysis of liposomes completely abolished cytotoxicity. We showed that the uptake of Man(11)-LPD100 by the murine DC line (DC2.4 cells) was at least 10-fold higher than that of Lac(6)-LPD100. A confocal microscopy study with DC2.4 cells expressing Rab5-EGFP or Rab7-EGFP, revealed that DNA uptake occurred through clathrin-mediated endocytosis. The transfection of DC2.4 cells with Man(11)-LPD100 containing DNA encoding luciferase gene gave luciferase activity two to three times higher (9 × 10(5) RLU/mg protein) than with non-mannosylated LPD100. In contrast to the latter, it was inhibited by 90% in the presence of mannose. Overall, the results indicate that mannosylated and histidylated LPD is a promising system for a selective DNA delivery in DCs.
我们首次报道了甘露糖基化和组氨酸化的脂多聚复合物(Man-LPD100)的制备,其对树突状细胞(DC)具有摄取和转染的选择性。Man-LPD100 是通过将甘露糖基化和组氨酸化的脂质体(Man-Lip100)添加到预先形成的聚乙二醇化组氨酸化多聚赖氨酸/DNA 多聚复合物上来制备的。Man-Lip100 由阳离子[O,O-二油酰基-N-(3N-(N-甲基咪唑啉碘化物)丙基)磷酰胺]脂质、中性[O,O-二油酰基-N-组氨酸磷酸酰胺]共脂质和β-D-甘露吡喃糖基-N-十二烷基十六烷酰胺(Man-脂质)组成。最佳情况下,获得了含有 11 mol% Man-脂质的 Man-Lip100。我们发现脂质体的透析完全消除了细胞毒性。我们表明,鼠源性 DC 系(DC2.4 细胞)摄取 Man(11)-LPD100 的至少 10 倍高于 Lac(6)-LPD100。用表达 Rab5-EGFP 或 Rab7-EGFP 的 DC2.4 细胞进行的共聚焦显微镜研究表明,DNA 摄取是通过网格蛋白介导的内吞作用发生的。用编码荧光素酶基因的 Man(11)-LPD100 转染 DC2.4 细胞可使荧光素酶活性提高 2 至 3 倍(9×105RLU/mg 蛋白),而非甘露糖基化的 LPD100 则提高 3 倍。与后者相比,甘露糖的存在抑制了 90%。总体而言,结果表明甘露糖基化和组氨酸化的 LPD 是一种有前途的用于在 DC 中进行选择性 DNA 递送的系统。