MicroRNA delivery for regenerative medicine

被引:123
作者
Peng, Bo [1 ]
Chen, Yongming [1 ]
Leong, Kam W. [1 ,2 ]
机构
[1] Sun Yat Sen Univ, Sch Chem & Chem Engn, Key Lab Polymer Composite & Funct Mat, Minist Educ, Guangzhou 510275, Guangdong, Peoples R China
[2] Columbia Univ, Dept Biomed Engn, New York, NY 10025 USA
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
MicroRNA; Non-viral vector; Regenerative medicine; Scaffold; Stem cells; Tissue engineering; Viral vector; MESENCHYMAL STEM-CELLS; NANOPARTICLE-MEDIATED DELIVERY; GENE DELIVERY; IN-VIVO; OSTEOGENIC DIFFERENTIATION; NEURONAL DIFFERENTIATION; RNA INTERFERENCE; CARDIOMYOCYTE PROLIFERATION; TRANSGENE EXPRESSION; CARDIAC REGENERATION;
D O I
10.1016/j.addr.2015.05.014
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
MicroRNA (miRNA) directs post-transcriptional regulation of a network of genes by targeting mRNA. Although relatively recent in development, many miRNAs direct differentiation of various stem cells including induced pluripotent stem cells (iPSCs), a major player in regenerative medicine. An effective and safe delivery of miRNA holds the key to translating miRNA technologies. Both viral and nonviral delivery systems have seen success in miRNA delivery, and each approach possesses advantages and disadvantages. A number of studies have demonstrated success in augmenting osteogenesis, improving cardiogenesis, and reducing fibrosis among many other tissue engineering applications. A scaffold-based approach with the possibility of local and sustained delivery of miRNA is particularly attractive since the physical cues provided by the scaffold may synergize with the biochemical cues induced by miRNA therapy. Herein, we first briefly cover the application of miRNA to direct stem cell fate via replacement and inhibition therapies, followed by the discussion of the promising viral and nonviral delivery systems. Next we present the unique advantages of a scaffold-based delivery in achieving lineage-specific differentiation and tissue development. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:108 / 122
页数:15
相关论文
共 204 条
[51]   Efficient inhibition of miR-155 function in vivo by peptide nucleic acids [J].
Fabani, Martin M. ;
Abreu-Goodger, Cei ;
Williams, Donna ;
Lyons, Paul A. ;
Torres, Adrian G. ;
Smith, Kenneth G. C. ;
Enright, Anton J. ;
Gait, Michael J. ;
Vigorito, Elena .
NUCLEIC ACIDS RESEARCH, 2010, 38 (13) :4466-4475
[52]   MicroRNA-24 Regulates Vascularity After Myocardial Infarction [J].
Fiedler, Jan ;
Jazbutyte, Virginija ;
Kirchmaier, Bettina C. ;
Gupta, Shashi K. ;
Lorenzen, Johan ;
Hartmann, Dorothee ;
Galuppo, Paolo ;
Kneitz, Susanne ;
Pena, John T. G. ;
Sohn-Lee, Cherin ;
Loyer, Xavier ;
Soutschek, Juergen ;
Brand, Thomas ;
Tuschl, Thomas ;
Heineke, Joerg ;
Martin, Ulrich ;
Schulte-Merker, Stefan ;
Ertl, Georg ;
Engelhardt, Stefan ;
Bauersachs, Johann ;
Thum, Thomas .
CIRCULATION, 2011, 124 (06) :720-U178
[53]   Most mammalian mRNAs are conserved targets of microRNAs [J].
Friedman, Robin C. ;
Farh, Kyle Kai-How ;
Burge, Christopher B. ;
Bartel, David P. .
GENOME RESEARCH, 2009, 19 (01) :92-105
[54]   MicroRNAs: key regulators of stem cells [J].
Gangaraju, Vamsi K. ;
Lin, Haifan .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2009, 10 (02) :116-125
[55]   Dicer inactivation in osteoprogenitor cells compromises fetal survival and bone formation, while excision in differentiated osteoblasts increases bone mass in the adult mouse [J].
Gaur, Tripti ;
Hussain, Sadiq ;
Mudhasani, Rajini ;
Parulkar, Isha ;
Colby, Jennifer L. ;
Frederick, Dana ;
Kream, Barbara E. ;
van Wijnen, Andre J. ;
Stein, Janet L. ;
Stein, Gary S. ;
Jones, Stephen N. ;
Lian, Jane B. .
DEVELOPMENTAL BIOLOGY, 2010, 340 (01) :10-21
[56]   The Role of Gene Therapy in Regenerative Surgery: Updated Insights [J].
Giatsidis, Giorgio ;
Dalla Venezia, Erica ;
Bassetto, Franco .
PLASTIC AND RECONSTRUCTIVE SURGERY, 2013, 131 (06) :1425-1435
[57]   Utilizing Cell-Matrix Interactions To Modulate Gene Transfer to Stem Cells Inside Hyaluronic Acid Hydrogels [J].
Gojgini, Shiva ;
Tokatlian, Talar ;
Segura, Tatiana .
MOLECULAR PHARMACEUTICS, 2011, 8 (05) :1582-1591
[58]   Biophysical and structural characterization of polyethylenimine-mediated siRNA delivery in vitro [J].
Grayson, Amy C. Richards ;
Doody, Anne M. ;
Putnam, David .
PHARMACEUTICAL RESEARCH, 2006, 23 (08) :1868-1876
[59]   Mammalian microRNAs predominantly act to decrease target mRNA levels [J].
Guo, Huili ;
Ingolia, Nicholas T. ;
Weissman, Jonathan S. ;
Bartel, David P. .
NATURE, 2010, 466 (7308) :835-U66
[60]   Formulation approaches to short interfering RNA and MicroRNA: Challenges and implications [J].
Guzman-Villanueva, Diana ;
El-Sherbiny, Ibrahim M. ;
Herrera-Ruiz, Dea ;
Vlassov, Alexander V. ;
Smyth, Hugh D. C. .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2012, 101 (11) :4046-4066