Reconstructed Stem Cell Nanoghosts: A Natural Tumor Targeting Platform

被引:263
作者
Furman, Naama E. Toledano [1 ]
Lupu-Haber, Yael [1 ]
Bronshtein, Tomer [1 ]
Kaneti, Limor [1 ]
Letko, Nitzan [1 ]
Weinstein, Eyal [1 ]
Baruch, Limor [1 ]
Machluf, Marcelle [1 ]
机构
[1] Technion Israel Inst Technol, Fac Biotechnol & Food Engn, IL-32000 Haifa, Israel
关键词
Nanoghosts; drug delivery; mesenchymal stem cells; cancer targeted therapy; DRUG-DELIVERY; S-TRAIL; CANCER; NANOPARTICLES; LIPOSOMES; SYSTEMS; GLIOMA;
D O I
10.1021/nl401376w
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
The ultimate goal in cancer therapy is achieving selective targeting of cancer cells. We report a novel delivery platform, based on nanoghosts (NGs) produced from the membranes of mesenchymal stem cells (MSCs). Encompassing MSC surface molecules, the MSC-NGs retained MSC-specific in vitro and in vivo tumor targeting capabilities and were cleared from blood-filtering organs. MSC-NGs were found to be biocompatible. Systemic administration of drug loaded MSC-NGs demonstrated 80% inhibition of human prostate cancer.
引用
收藏
页码:3248 / 3255
页数:8
相关论文
共 42 条
[1]
Mesenchymal stem cell therapy: Two steps forward, one step back [J].
Ankrum, James ;
Karp, Jeffrey M. .
TRENDS IN MOLECULAR MEDICINE, 2010, 16 (05) :203-209
[2]
Prediction of membrane protein orientation in lipid bilayers: a theoretical approach [J].
Basyn, F ;
Charloteaux, B ;
Thomas, A ;
Brasseur, R .
JOURNAL OF MOLECULAR GRAPHICS & MODELLING, 2001, 20 (03) :235-244
[3]
Immunologic consequences of multiple, high-dose administration of allogeneic mesenchymal stem cells to baboons [J].
Beggs, Kirstin J. ;
Lyubimov, Alex ;
Borneman, Jade N. ;
Bartholomew, Amelia ;
Moseley, Annemarie ;
Dodds, Robert ;
Archambault, Michael P. ;
Smith, Alan K. ;
McIntosh, Kevin R. .
CELL TRANSPLANTATION, 2006, 15 (8-9) :711-721
[4]
Clinical chemistry reference database for Wistar rats and C57/BL6 mice [J].
Boehm, Olaf ;
Zur, Berndt ;
Koch, Alexander ;
Tran, Nguyen ;
Freyenhagen, Rainer ;
Hartmann, Matthias ;
Zacharowski, Kai .
BIOLOGICAL CHEMISTRY, 2007, 388 (05) :547-554
[5]
Cell derived liposomes expressing CCR5 as a new targeted drug-delivery system for HIV infected cells [J].
Bronshtein, Tomer ;
Toledano, Naama ;
Danino, Dganit ;
Pollack, Shimon ;
Machluf, Marcelle .
JOURNAL OF CONTROLLED RELEASE, 2011, 151 (02) :139-148
[6]
Liposome based systems for systemic siRNA delivery: Stability in blood sets the requirements for optimal carrier design [J].
Buyens, Kevin ;
De Smedt, Stefaan C. ;
Braeckmans, Kevin ;
Demeester, Joseph ;
Peeters, Liesbeth ;
van Grunsven, Leo A. ;
du Jeu, Xavier de Mollerat ;
Sawant, Rupa ;
Torchilin, Vladimir ;
Farkasova, Katarina ;
Ogris, Manfred ;
Sanders, Niek N. .
JOURNAL OF CONTROLLED RELEASE, 2012, 158 (03) :362-370
[7]
PEGylation of a vesicular stomatitis virus G pseudotyped lentivirus vector prevents inactivation in serum [J].
Croyle, MA ;
Callahan, SM ;
Auricchio, A ;
Schumer, G ;
Linse, KD ;
Wilson, JM ;
Brunner, LJ ;
Kobinger, GP .
JOURNAL OF VIROLOGY, 2004, 78 (02) :912-921
[8]
Peritoneal retention of liposomes: Effects of lipid composition, PEG coating and liposome charge [J].
Dadashzadeh, S. ;
Mirahmadi, N. ;
Babaei, M. H. ;
Vali, A. M. .
JOURNAL OF CONTROLLED RELEASE, 2010, 148 (02) :177-186
[9]
Impact of Nanotechnology on Drug Delivery [J].
Farokhzad, Omid C. ;
Langer, Robert .
ACS NANO, 2009, 3 (01) :16-20
[10]
Caspase-independent phosphatidylserine exposure during apoptosis of primary T lymphocytes [J].
Ferraro-Peyret, C ;
Quemeneur, L ;
Flacher, M ;
Revillard, JP ;
Genestier, L .
JOURNAL OF IMMUNOLOGY, 2002, 169 (09) :4805-4810