Fabrication of Synthetic Mesenchymal Stem Cells for the Treatment of Acute Myocardial Infarction in Mice

被引:175
作者
Luo, Lan [1 ]
Tang, Junnan [3 ,6 ,7 ]
Nishi, Kodai [2 ]
Yan, Chen [1 ]
Dinh, Phuong-Uyen [4 ,5 ,6 ,7 ]
Cores, Jhon [7 ]
Kudo, Takashi [2 ]
Zhang, Jinying [3 ,6 ]
Li, Tao-Sheng [1 ]
Cheng, Ke [1 ,4 ,5 ,6 ,7 ,8 ]
机构
[1] Nagasaki Univ, Grad Sch Biomed Sci, Dept Stem Cell Biol, Nagasaki, Japan
[2] Nagasaki Univ, Atom Bomb Dis Inst, Dept Radioisotope Med, Nagasaki, Japan
[3] Zhengzhou Univ, Affiliated Hosp 1, Dept Cardiol, Zhengzhou, Henan, Peoples R China
[4] Univ N Carolina, Dept Mol Biomed Sci, Raleigh, NC USA
[5] Univ N Carolina, Comparat Med Inst, Raleigh, NC USA
[6] Univ N Carolina, Dept Biomed Engn, Raleigh, NC USA
[7] North Carolina State Univ, Raleigh, NC 27695 USA
[8] North Carolina State Univ, Eshelman Sch Pharm, Mol Pharmaceut Div, Raleigh, NC 27695 USA
关键词
artificial cells; mesenchymal stem cells; myocardial infarction; regeneration; stem cells; tissue engineering; CARDIOVASCULAR-DISEASE; CARDIAC-DISEASE; THERAPY; EXOSOMES; REPAIR; HEART; NANOPARTICLES; REGENERATION; MECHANISMS;
D O I
10.1161/CIRCRESAHA.116.310374
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Rationale: Stem cell therapy faces several challenges. It is difficult to grow, preserve, and transport stem cells before they are administered to the patient. Synthetic analogs for stem cells represent a new approach to overcome these hurdles and hold the potential to revolutionize regenerative medicine. Objective: We aim to fabricate synthetic analogs of stem cells and test their therapeutic potential for treatment of acute myocardial infarction in mice. Methods and Results: We packaged secreted factors from human bone marrow-derived mesenchymal stem cells (MSC) into poly(lactic-co-glycolic acid) microparticles and then coated them with MSC membranes. We named these therapeutic particles synthetic MSC (or synMSC). synMSC exhibited a factor release profile and surface antigens similar to those of genuine MSC. synMSC promoted cardiomyocyte functions and displayed cryopreservation and lyophilization stability in vitro and in vivo. In a mouse model of acute myocardial infarction, direct injection of synMSC promoted angiogenesis and mitigated left ventricle remodeling. Conclusions: We successfully fabricated a synMSC therapeutic particle and demonstrated its regenerative potential in mice with acute myocardial infarction. The synMSC strategy may provide novel insight into tissue engineering for treating multiple diseases.
引用
收藏
页码:1768 / 1775
页数:8
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