Peptide modified mesenchymal stem cells as targeting delivery system transfected with miR-133b for the treatment of cerebral ischemia

被引:60
作者
Huang, Bing [1 ]
Jiang, Xin-Chi [1 ]
Zhang, Tian-Yuan [1 ]
Hu, Yu-Lan [1 ]
Tabata, Yasuhiko [2 ]
Chen, Zhong [3 ]
Pluchino, Stefano [4 ]
Gao, Jian-Qing [1 ,5 ]
机构
[1] Zhejiang Univ, Inst Pharmaceut, Coll Pharmaceut Sci, Hangzhou, Zhejiang, Peoples R China
[2] Kyoto Univ, Inst Frontier Med Sci, Dept Biomat, Kyoto, Japan
[3] Zhejiang Univ, Dept Pharmacol, Coll Pharmaceut Sci, Key Lab Med Neurobiol,Minist Hlth China, Hangzhou, Zhejiang, Peoples R China
[4] Univ Cambridge, Dept Clin Neurosci, Wellcome Trust Med Res Council Stem Cell Inst, Cambridge, Cambs, England
[5] Zhejiang Univ, Dr Li Dak Sum & Yip Yio Chin Ctr Stem Cell & Rege, Hangzhou, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Mesenchymal stem cells; Targeting delivery system; Cerebral ischemia; Membrane coating; Peptide-based cell targeting; MiR-133b transfection Stem; cell-based targeting therapy; MARROW STROMAL CELLS; LEUKOTRIENE RECEPTOR-1 ANTAGONIST; HUMAN MYOCARDIAL-INFARCTION; CLOSED-HEAD INJURY; NONVIRAL TRANSFECTION; BEHAVIORAL DEFICITS; FUNCTIONAL RECOVERY; ARTERY OCCLUSION; PROGENITOR CELLS; RAT MODEL;
D O I
10.1016/j.ijpharm.2017.08.073
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Mesenchymal stem cells (MSCs) have been regarded as potential targeting vehicles and demonstrated to exert therapeutic benefits for brain diseases. Direct homing to diseased tissue is crucial for stem cell-based therapy. In this study, a peptide-based targeting approach was established to enhance cell homing to cerebral ischemic lesion. Palmitic acid-peptide painted onto the cell membrane was able to direct MSCs to ischemic tissues without any observed cell cytotoxicity and influence on differentiation, thus reducing accumulation of cells in peripheral organs and increasing engraftment of cells in the targeted tissues. With enhanced cell homing, MSCs were used to deliver miR-133b to increase the expression level of miR-133b in an ischemic lesion and further improve therapeutic effects. This study is the first to develop MSCs co-modified with targeting peptide and microRNAs as potential targeting therapeutic agents. This targeting delivery system is expected to be applicable to other cell types and other diseases aside from stroke.
引用
收藏
页码:90 / 100
页数:11
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