Affiliations 

  • 1 Department of Companion Animal Medicine and Surgery, Faculty of Veterinary Medicine, Universiti Putra, Malaysia; Department of Basic Veterinary Sciences, Faculty of Veterinary and Animal Sciences, Gomal University D.I.Khan, Pakistan
  • 2 Department of Companion Animal Medicine and Surgery, Faculty of Veterinary Medicine, Universiti Putra, Malaysia; Department of Surgery and Theriogenology, College of Veterinary Medicine, University of Mosul, Iraq
  • 3 Department of Companion Animal Medicine and Surgery, Faculty of Veterinary Medicine, Universiti Putra, Malaysia
  • 4 Department of Chemistry, Faculty of Science, Universiti Putra, Malaysia
  • 5 Department of Pre-Clinical Veterinary Studies, Faculty of Veterinary Medicine, Universiti Putra, Malaysia
  • 6 Department of Veterinary Pathology and Microbiology, Faculty of Veterinary Medicine, Universiti Putra, Malaysia
  • 7 Department of Companion Animal Medicine and Surgery, Faculty of Veterinary Medicine, Universiti Putra, Malaysia. Electronic address: loqman@upm.edu.my
Cryobiology, 2020 02 01;92:26-33.
PMID: 31580830 DOI: 10.1016/j.cryobiol.2019.09.012

Abstract

A number of living creatures in the Antarctic region have developed characteristic adaptation of cold weather by producing antifreeze proteins (AFP). Antifreeze peptide (Afp1m) fragment have been designed in the sequence of strings from native proteins. The objectives of this study were to assess the properties of Afp1m to cryopreserve skin graft at the temperature of -10 °C and -20 °C and to assess sub-zero injuries in Afp1m cryopreserved skin graft using light microscopic techniques. In the present study, a process was developed to cryopreserve Sprague-Dawley (SD) rat skin grafts with antifreeze peptide, Afp1m, α-helix peptide fragment derived from Glaciozyma antractica yeast. Its viability assessed by different microscopic techniques. This study also described the damages caused by subzero temperatures (-10 and -20 °C) on tissue cryopreserved in different concentrations of Afp1m (0.5, 1, 2, 5 and 10 mg/mL) for 72 h. Histological scores of epidermis, dermis and hypodermis of cryopreserved skin grafts showed highly significant difference (p 

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.