Efficient intracellular drug-targeting of macrophages using stealth liposomes directed to the hemoglobin scavenger receptor CD163

被引:116
作者
Etzerodt, Anders [1 ]
Maniecki, Maciej Bogdan [2 ]
Graversen, Jonas Heilskov [3 ]
Moller, Holger Jon [2 ]
Torchilin, Vladimir P. [4 ]
Moestrup, Soren Kragh [1 ,2 ]
机构
[1] Aarhus Univ, Dept Biomed, DK-8000 Aarhus C, Denmark
[2] Aarhus Univ Hosp, Dept Clin Biochem, DK-8000 Aarhus C, Denmark
[3] Cytoguide Aps, Aarhus, Denmark
[4] Northeastern Univ, Bouve Coll Hlth Sci, Sch Pharm, Boston, MA 02115 USA
基金
欧洲研究理事会;
关键词
CD163; Stealth liposomes; Macrophage; Inflammation; Tumor-associated macrophages; Cancer; TUMOR-ASSOCIATED MACROPHAGES; CANCER-CHEMOTHERAPY; MONOCLONAL-ANTIBODY; ANTITUMOR-ACTIVITY; EXPRESSION; CELLS; DELIVERY; INFECTION; DISEASE; ANTIGEN;
D O I
10.1016/j.jconrel.2012.01.034
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
The hemoglobin scavenger receptor CD163 is exclusively expressed in the monocytic lineage and preferentially in tissue resident macrophages of the M2 phenotype and in macrophages in sites of inflammation and tumor growth. In the present study we have designed liposomes specifically targeting CD163 by hydrophobic linkage of CD163-binding monoclonal antibodies to polyethylene glycol-coated liposomes ('stealth liposomes'). Targeting to the endocytic CD163 protein greatly increased the uptake of liposomes in CD163 transfected cells and macrophages as visualized by confocal microscopy and flow cytometry of cells exposed to CD163 targeting liposomes loaded with calcein. Strong cytotoxic effects were seen in CD163-expressing human monocytes by using the chemotherapeutic agent doxorubicin as cargo of the liposomes. In conclusion, the use of stealth liposomes modified to recognize CD163 is a potential way to target drugs to macrophages that support inflammatory and malignant processes. (C) 2012 Elsevier B. V. All rights reserved.
引用
收藏
页码:72 / 80
页数:9
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