MRI tracking of human Wharton’s jelly stem cells seeded onto acellular dermal matrix labeled with superparamagnetic iron oxide nanoparticles in burn wounds

Author:

Mehrabani Davood1234,Nazempour Mehra5,Mehdinavaz-Aghdam Rouhollah6,Hashemi Seyedeh-Sara2,Jalli Reza7,Moghadam Mahdi Saeedi7,Zare Shahrokh18,Jamhiri Iman1,Moayedi Javad3,Karimi-Busheri Feridoun9ORCID

Affiliation:

1. Shiraz University of Medical Sciences Stem Cell Technology Research Center, , Shiraz, Fars T6G 2E1, 71348-14336 , Iran

2. Shiraz University of Medical Sciences Burn and Wound Healing Research Center, , Shiraz, Fars 71987-74731 , Iran

3. Shiraz University of Medical Sciences Comparative and Experimental Medicine Center, , Shiraz, Fars 71348-14336 , Iran

4. University of Alberta Li Ka Shing Center for Health Research and Innovation, , Edmonton, Alberta , Canada

5. Islamic Azad University Department of Biomedical and Tissue Engineering, Science and Research Branch, , Tehran , Iran

6. University of Tehran School of Metallurgy and Materials Engineering, College of Engineering, , Tehran 1417614411 , Iran

7. Shiraz University of Medical Sciences Medical Imaging Research Center, Department of Radiology, , Shiraz, Fars 71348-14336 , Iran

8. Islamic Azad University Department of Biochemistry, School of Biotechnology and Agriculture, Shiraz Branch, , Shiraz, Fars 71987-74731 , Iran

9. University of Alberta Department of Oncology, Faculty of Medicine, , Edmonton, Alberta, T6G 1Z2 , Canada

Abstract

Abstract Background In vivo cell tracking after transplantation in regenerative medicine remains an unmet challenge and limits current understanding of the wound healing mechanism through cell-based therapies. This study investigated tracking of human Wharton’s jelly stem cells (hWJSCs) seeded onto an acellular dermal matrix (ADM) and labeled with superparamagnetic iron oxide nanoparticles (SPIONs) by magnetic resonance imaging (MRI) in burn injury. Method The hWJSCs were characterized and assessed for growth kinetics. A total of 30 rats were enrolled in three equal groups. Group 1 underwent scald burn injury left without treatment, the group 2 was treated by an ADM that was prepared from cosmetic surgery skin samples and the group 3 received hWJSCs labeled with SPIONs seeded onto an ADM. Tensile strength was evaluated before and after interventions, real time PCR assessed apoptosis, and Prussian blue staining, scanning electron microscopy (SEM) and MRI were used for the tracking of labeled cells. Results The hWJSCs exhibited mesenchymal stem cell properties. Population doubling time was 40.1 hours. SPIONs did not show any toxic effect. The hWJSCs seeded onto an ADM decreased Bax and increased Bcl-2 gene expression. Internalization of SPIONs within hWJSCs was confirmed by Prussian blue staining, SEM and MRI until day 21. There was a significant difference between the Young’s moduli of normal skin and the group receiving hWJSCs seeded onto an ADM. Histological observations and SEM imaging confirmed that MRI is an accurate method to track SPION-labeled hWJSCs in vivo. Conclusions This study showed that SPION labeling coupled with MRI can be used to further understand the fate of stem cells after transplantation in a burn model.

Publisher

Oxford University Press (OUP)

Subject

Critical Care and Intensive Care Medicine,Dermatology,Biomedical Engineering,Emergency Medicine,Immunology and Allergy,Surgery

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