iPS cell transplantation in a mouse model – A semiquantitative assessment

Authors

  • Ong Patrick Yit Han Tissue Culture Engineering Research Group, Department of Bioprocess & Polymer Engineering, School of Chemical and Energy Engineering, Faculty of Engineering, Universiti Teknologi Malaysia
  • Zanariah Hashim Department of Bioprocess & Polymer Engineering, School of Chemical and Energy Engineering, Faculty of Engineering, Universiti Teknologi Malaysia, Malaysia. https://orcid.org/0000-0001-9347-9951
  • Mohd Effendy Abd Wahid School of Fisheries and Aquaculture, Universiti Malaysia Terengganu, Malaysia.
  • Diana Bee Lan Ong Pathology’s Unit for Research Support and Education, Department of Pathology, Faculty of Medicine, Universiti Malaya, Malaysia
  • Nur Adibah Bakkery Pathology’s Unit for Research Support and Education, Department of Pathology, Faculty of Medicine, Universiti Malaya, Malaysia.
  • Reena Rahayu Md Zin Department of Pathology, Faculty of Medicine, Universiti Kebangsaan Malaysia, Malaysia.
  • Nur Maya Sabrina Tizen Liam Department of Pathology, Faculty of Medicine, Universiti Kebangsaan Malaysia, Malaysia.
  • Faridah Abd Rahman Department of Pathology, Faculty of Medicine, Universiti Kebangsaan Malaysia, Malaysia.
  • Muaatamarulain Mustangin Department of Pathology, Faculty of Medicine, Universiti Kebangsaan Malaysia, Malaysia.
  • Norazwin Hajri Institute of Marine Biotechnology, Universiti Malaysia Terengganu, Malaysia.
  • Fadzilah Adibah Abdul Majid Institute of Marine Biotechnology, Universiti Malaysia Terengganu, Malaysia

DOI:

https://doi.org/10.11113/mjfas.v16n6.1875

Keywords:

Wound and Injuries, Induced Pluripotent Stem Cells, Skin, Transplants, Cell Transplantation

Abstract

This study was carried out to determine the effectiveness of induced pluripotent stem (iPS) cell-transplantation as a therapy on wound healing using a splinted wound mouse model. Eighteen clinically healthy female mice were treated with 1μg/g of dexamethasone intramuscular injection once a day for three consecutive days to induce immunosuppression. Under anaesthesia, two sterile wounds were made on shaved backs of each mouse via biopsy punch. With a gap of 20 mm in-between, six injections were delivered once, around the two wounds before the wounds were adhered with splints and wound dressing. The mice were divided into two groups; Group A was given 7 × 105 iPS cells in each injection, and while Group B were injected with 0.9% sodium chloride instead. Wound closure rates were determined through timed scaled photography and analyses with GNU Image Manipulation Program. Three mice from each group were euthanised every 7 days post-wounding, immediately after which wound beds and blood were harvested. Wound beds were fixed, processed, blocked, and sectioned. Sections were stained with H&E; Masson’s Trichrome; and immunolabeled for CD31 and CD68; and then examined under a compound microscope subjected to a scoring scheme. From this semiquantitative assessment, Group A sections scored better in angiogenesis on day 7 (p = 0.057), a vital process in the proliferation stage, and hypodermis regeneration on day 21 (p = 0.006), which suggests the wound healing is complete. Together, these findings suggest Group A was ahead in the process of wound healing; although results from lymphocyte count, fibroblast count, granulation tissue, collagen, and wound closure were not statistically significant.

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Published

28-12-2020