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A new methodology of mesenchymal stem cell expansion using magnetic nanoparticles
Authors:Akira Ito  Eri Hibino  Hiroyuki Honda  Ken-ichiro Hata  Hideaki Kagami  Minoru Ueda  Takeshi Kobayashi  
Institution:

a Department of Biotechnology, School of Engineering, Nagoya University, Nagoya 464-8603, Japan

b Genetic and Regenerative Medical Center, School of Medicine, Nagoya University, Nagoya 466-8550, Japan

c J-TEC Endowed Chair in Tissue Engineering, School of Medicine, Nagoya University, Nagoya 466-8550, Japan

d Department of Oral and Maxillofacial Surgery, School of Medicine, Nagoya University, Nagoya 466-8550, Japan

Abstract:Mesenchymal stem cells (MSCs), which can differentiate into multiple mesodermal tissues, may be useful for autologous cell transplantation, if MSCs, which are isolated from bone marrow in small numbers, can be expanded in vitro. We developed a combined methodological approach to enrich and proliferate MSCs in vitro using magnetic nanoparticles. Our magnetite cationic liposomes (MCLs), which have a positive surface charge in order to improve adsorption, accumulated in MSCs at a concentration of 20 pg of magnetite per cell. The MCLs exhibited no toxicity against MSCs in proliferation and differentiation to osteoblasts and adipocytes. The MSCs magnetically labeled by MCLs were enriched using magnets and then cultured, resulting in much higher density (seeding density, 1000 cells/cm2) than in ordinary culture (seeding density, 18 cells/cm2). When MSCs were seeded at high density using MCLs, there was a 5-fold increase in the number of cells, compared to culture prepared without MCLs. Our results suggest that this novel culture method using magnetic nanoparticles can be used to efficiently expand MSCs for clinical application.
Keywords:Mesenchymal stem cells  Cell culture  Proliferation  Liposomes  Magnetic particles
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