4.7 Article

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

期刊

CIRCULATION RESEARCH
卷 120, 期 11, 页码 1768-1775

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/CIRCRESAHA.116.310374

关键词

artificial cells; mesenchymal stem cells; myocardial infarction; regeneration; stem cells; tissue engineering

资金

  1. National Institute of Health [R01 HL123920, HL137093]
  2. Ministry of Education, Science, Sports, Culture and Technology of Japan
  3. Network-Type Joint Usage/Research Center for Radiation Disaster Medical Science of Hiroshima University
  4. Nagasaki University
  5. Fukushima Medical University
  6. UNC General Assembly Research Opportunities Initiative award
  7. Grants-in-Aid for Scientific Research [26461857, 16H05174, 16H03062, 15K15509, 17K10447] Funding Source: KAKEN

向作者/读者索取更多资源

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.

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