Differentiation Induction of Mesenchymal Stem Cells by a Au Delivery Platform

Author:

Yang Meng-Yin1234ORCID,Chiu Cheng-Di56ORCID,Ke Yi-Chun7,Yang Yi-Chin1ORCID,Chang Kai-Bo7,Chen Chien-Min89,Lee Hsu-Tung14,Tang Chien-Lun1,Liu Bai-Shuan10,Hung Huey-Shan711ORCID

Affiliation:

1. Department of Neurosurgery, Neurological Institute, Taichung Veterans General Hospital, Taichung 407219, Taiwan

2. Graduate Institute of Medical Sciences, National Defense Medical Center, Taipei 11490, Taiwan

3. College of Nursing, Central Taiwan University of Science and Technology, Taichung 406053, Taiwan

4. Department of Post-Baccalaureate Medicine, College of Medicine, National Chung Hsing University, Taichung 402202, Taiwan

5. Department of Neurosurgery, China Medical University Hospital, Taichung 404327, Taiwan

6. Spine Center, China Medical University Hospital, Taichung 404327, Taiwan

7. Graduate Institute of Biomedical Science, China Medical University, Taichung 404333, Taiwan

8. Division of Neurosurgery, Department of Surgery, Changhua Christian Hospital, Changhua 50006, Taiwan

9. Department of Leisure Industry Management, National Chin-Yi University of Technology, Taichung 411030, Taiwan

10. Department of Medical Imaging and Radiological Sciences, Central Taiwan University of Science and Technology, Taichung 406053, Taiwan

11. Translational Medicine Research, China Medical University Hospital, Taichung 404327, Taiwan

Abstract

Au decorated with type I collagen (Col) was used as a core material to cross-link with stromal cell-derived factor 1α (SDF1α) in order to investigate biological performance. The Au-based nanoparticles were subjected to physicochemical determination using scanning electron microscopy (SEM), dynamic light scattering (DLS) and ultraviolet–visible (UV-Vis) and Fourier-transform infrared spectroscopy (FTIR). Mesenchymal stem cells (MSCs) were used to evaluate the biocompatibility of this nanoparticle using the MTT assay and measuring reactive oxygen species (ROS) production. Also, the biological effects of the SDF-1α-conjugated nanoparticles (Au-Col-SDF1α) were assessed and the mechanisms were explored. Furthermore, we investigated the cell differentiation-inducing potential of these conjugated nanoparticles on MSCs toward endothelial cells, neurons, osteoblasts and adipocytes. We then ultimately explored the process of cell entry and transportation of the nanoparticles. Using a mouse animal model and retro-orbital sinus injection, we traced in vivo biodistribution to determine the biosafety of the Au-Col-SDF1α nanoparticles. In summary, our results indicate that Au-Col is a promising drug delivery system; it can be used to carry SDF1α to improve MSC therapeutic efficiency.

Funder

Taichung Veterans General Hospital

Ministry of Science and Technology

Publisher

MDPI AG

Subject

General Medicine

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