Establishing a Xenograft Model with CD-1 Nude Mice to Study Human Skin Wound Repair

Author:

Abbas Darren B.1,Griffin Michelle1,Fahy Evan J.1,Spielman Amanda F.1,Guardino Nicholas J.1,Pu Adrian1,Lintel Hendrik1,Lorenz H. Peter1,Longaker Michael T.12,Wan Derrick C.1

Affiliation:

1. Hagey Laboratory for Pediatric Regenerative Medicine

2. Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine.

Abstract

Background: A significant gap exists in the translatability of small-animal models to human subjects. One important factor is poor laboratory models involving human tissue. Thus, the authors have created a viable postnatal human skin xenograft model using athymic mice. Methods: Discarded human foreskins were collected following circumcision. All subcutaneous tissue was removed from these samples sterilely. Host CD-1 nude mice were then anesthetized, and dorsal skin was sterilized. A 1.2-cm-diameter, full-thickness section of dorsal skin was excised. The foreskin sample was then placed into the full-thickness defect in the host mice and sutured into place. Xenografts underwent dermal wounding using a 4-mm punch biopsy after engraftment. Xenografts were monitored for 14 days after wounding and then harvested. Results: At 14 days postoperatively, all mice survived the procedure. Grossly, the xenograft wounds showed formation of a human scar at postoperative day 14. Hematoxylin and eosin and Masson trichome staining confirmed scar formation in the wounded human skin. Using a novel artificial intelligence algorithm using picrosirius red staining, scar formation was confirmed in human wounded skin compared with the unwounded skin. Histologically, CD31+ immunostaining confirmed vascularization of the xenograft. The xenograft exclusively showed human collagen type I, CD26+, and human nuclear antigen in the human scar without any staining of these human markers in the murine skin. Conclusion: The proposed model demonstrates wound healing to be a local response from tissue resident human fibroblasts and allows for reproducible evaluation of human skin wound repair in a preclinical model. Clinical Relevance Statement: Radiation-induced fibrosis is a widely prevalent clinical phenomenon without a well-defined treatment at this time. This study will help establish a small-animal model to better understand and develop novel therapeutics to treat irradiated human skin.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Surgery

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