Potentiated therapeutic angiogenesis by primed human mesenchymal stem cells in a mouse model of hindlimb ischemia

Author:

Lee Eun Ju1,Park Hwan-Woo2,Jeon Hyo-Jin2,Kim Hyo-Soo134,Chang Mi-Sook5

Affiliation:

1. National Research Laboratory for Cardiovascular Stem Cells & IRICT, Seoul National University Hospital, Seoul, Republic of Korea

2. Department of Oral Anatomy, School of Dentistry & Dental Research Institute, Seoul National University, 28 Yeongeon-Dong, Jongno-Gu, Seoul 110-749, Republic of Korea

3. Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea

4. World Class University Program, Molecular Medicine & Biopharmaceutical Science, Seoul National University, IRICT, Seoul National University Hospital, 28 Yongon-dong, Chongno-gu, Seoul 110-744, Republic of Korea

5. Neuroscience Research Institute, Seoul National University, Seoul, Republic of Korea.

Abstract

Background: Human bone marrow-derived mesenchymal stem cells (hMSCs) are advantageous for cell-based therapy to treat ischemic diseases owing to their capacity to secrete various paracrine factors with potent angiogenic activity. Materials & methods: In this study, we describe a method to increase secreted levels of VEGF and HGF from hMSCs without genetic modification. Results: We demonstrated that transplantation of primed hMSCs into ischemic limbs led to significantly greater improvements in tissue perfusion and limb salvage by increasing capillary formation compared with nonprimed hMSCs. The primed hMSCs also exhibited greater survival in vivo and secreted human VEGF and HGF in the ischemic tissue, supporting enhanced angiogenesis and cell survival. Conclusion: These findings indicate that priming hMSCs via methods described in this study enhances secretion of critical proangiogenic factors resulting in an enhanced therapeutic effect of cells for the treatment of ischemic diseases.

Publisher

Future Medicine Ltd

Subject

Embryology,Biomedical Engineering

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