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Encyclopedia of Experiments

A Technique for Human Skin Grafting in a Mouse Model

Overview

This video demonstrates a method for grafting human skin onto an immunodeficient mouse with a suppressed neutrophil response. The method involves applying human split-thickness skin to the mouse's graft bed, sealing it, and covering it for recovery. Eventually, the human skin adheres to the mouse's skin, establishing vascularization and circulation, resulting in a successful skin xenograft.

Protocol

All procedures involving animal models have been reviewed by the local institutional animal care committee and the JoVE veterinary review board.

1. Processing of donor human skin sample

NOTE: The human skin sample used in this transplant was a large sample collected from the abdomen of a healthy patient. The sample must be at least 15 cm x 7.5 cm. Size limitations may affect the number of mice for which skin is available and the choice of graft size.

  1. Maintain the skin sample at cold temperatures (on ice; 4°C) before preparation and grafting. Keep the sample moist in a closed specimen collection cup with the gauze soaked in phosphate-buffered saline (PBS).
    NOTE: Storing the skin sample at 4 °C for longer than 2 days is not recommended. However, reports exist where the skin samples are stored for a longer time.
    CAUTION: Treat all human tissue with standard biohazard precautions.
  2. Prepare to dermatome the human skin sample in a sterilized negative pressure tissue culture hood on a sterilized dissection board.
  3. Place the skin sample, epidermis side up, on the dissection board. Wipe the epidermis with a sterile alcohol prep pad and then with PBS.
  4. Pin the closer edge of the skin in place with a 1.5-inch dissecting T-pin (see Table of Materials).
  5. Dermatome the skin specimen at a 400 µm thickness, applying steady pressure while cutting forward at a 30°-45° angle. Follow all instrument-specific instructions and safety measures (see Table of Materials).
    NOTE: For details on the dermatome technique, please see a previously published report.
  6. Prepare a 100 mm x 20 mm Petri dish by placing a sterile gauze soaked in sterile PBS at the bottom of the dish. Place the skin, epidermis side up, onto the wet gauze.
  7. Seal and cover the plate edges with a semi-transparent sealing film (see Table of Materials) to ensure the sample is not contaminated. Store the sample at 4° C prior to grafting.

2. Pre-surgery conditioning and preparation

  1. Prepare the sterile instruments and a sterile surgical station for grafting. Use autoclaved paper towels as sterile surfaces for instrument and mouse placement.
    NOTE: Mice may be grafted after weaning but are preferably grafted between 8-10 weeks of age. Mice of either sex may be grafted.
  2. Perform the surgical preparation, such as hair removal, in an area physically separated from the surgical station.
  3. Prepare the anti-GR1 (see Table of Materials) by diluting it to 1 mg/mL in sterile saline. Dose each mouse with 100 µg/100 µL of the anti-GR1 solution intraperitoneally following anesthesia induction.
  4. Anesthetize the mice, one at a time, with isoflurane or other institutionally approved anesthetics.
    NOTE: Isoflurane needs to be given at a 3%-5% concentration during induction. Once the mouse is immobile, lower the isoflurane concentration to 1%-3% to affect the duration of the surgery.
    1. Monitor the mouse for appropriate depth of anesthesia by observing respiratory rate, absence of toe-pinch response, and appropriate pink coloration of ears and mouth.
      CAUTION: Use appropriate anesthetic machinery and scavenging methods, and avoid exposure to isoflurane vapors.
  5. Transfer the mouse to a heating pad or another heat source (see Table of Materials).
  6. Administer the ophthalmic ointment by dabbing a small drop of ointment on the eye with a gloved finger.
  7. Administer analgesics Buprenorphine (0.08 mg/kg) and Carprofen (5 mg/kg) (see Table of Materials) subcutaneously by pinching the skin and injecting at an angle parallel to the body.   
    NOTE: Prepare the pre-treatment analgesia following institutional protocols. Follow institutional guidelines for the selection and administration of analgesics. The method of analgesia used in this study is outlined in step 2.7 and Figure 1.
  8. Administer the anti-GR1 (prepared in step 2.4) intraperitoneally by slightly lifting the mouse by the tail, exposing the abdomen, and injecting at a 30° angle using an insulin 1 mL (12.7 mm) syringe.
  9. Use animal-safe electric clippers (see Table of Materials) to shave the middle and upper portions of the dorsal side of the mouse.
  10. Clear all the hair and apply a generous amount of hair removal ointment onto the shaved skin for 30 s to 1 min.
  11. Completely wipe away hair removal ointment with a paper towel and PBS.

3. Transplantation procedure

  1. Transfer the mouse to a secondary surgical location, away from the hair removal station.
  2. Sterilize the surgical site with the iodine swab stick in a circular motion, starting in the middle and working out toward the edge of the depilated area.
  3. Place a piece of sterile plastic wrap over the mouse and cut a window in the plastic slightly larger than the size of the area to be grafted.
  4. Cut a rectangle-shaped 10 mm x 10 mm portion of donor skin to be grafted with a scalpel. Do this by firmly holding the donor skin in place with the backside of the forceps and cutting alongside the forceps with the scalpel.
  5. Using the surgical scissors, snip a rectangular area of mouse skin matching the size of the donor skin piece, creating a graft bed. Use forceps to pull the skin away from the body, and cut the skin with the scissors angled away from the body to avoid cutting deeply into the facia.
  6. Place the donor skin piece, epidermis side up, onto the prepared graft bed.
  7. Using the back of the forceps, manipulate the skin, sliding back and forth until the donor skin lies completely flat against the graft bed.
  8. Add drops of surgical glue tissue adhesive (see Table of Materials) where the donor skin meets the mouse skin and hold the mouse and donor skin together with forceps for 1-2 s so that the glue adheres to the tissues. Completely seal the edge of the graft and allow for the glue to dry fully.
  9. Bandage the mice (Figure 2) following the steps below.
    1. Cut a piece of petrolatum gauze (see Table of Materials) large enough to cover the graft area completely.
    2. Cover the graft with the petrolatum gauze and lightly press the gauze against the skin using forceps.
    3. Cut a strip of a transparent film dressing lengthwise so that the width is large enough to cover the mouse's wound.
    4. Firmly press the transparent film dressing, adhesive side down, over the gauze. Quickly roll the mouse to wrap the dressing completely around the torso, ensuring it fits tightly without impeding respiration, and all limbs are free for movement.
    5. Place the mouse in a recovery cage and monitor it until it is alert and moving around. Provide a heat source on part of the cage for at least 15 min following recovery.
      NOTE: The animals are expected to recover within 1-5 min after placing them in the recovery cage.

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Representative Results

Figure 1
Figure 1: Timeline of the protocol adopted for the xenograft study.

Figure 2
Figure 2: Method for bandaging mouse after surgery. The mouse is wrapped tightly in petrolatum gauze and transparent film dressing while under anesthesia. (A) Petrolatum gauze is placed over an area slightly larger than the surgical wound. (B) The transparent film dressing is prepared: a long strip is cut slightly wider than the petrolatum gauze. The backing covering the adhesive side of the transparent film dressing is partially removed. (C) The adhesive side of the film is firmly pressed against the back of the mouse, leaving an inch of space on the front end of the film. (D) The mouse is turned on its back. The overhanging front portion of the film is pressed onto the mouse, and the backing is removed. (E) The mouse is tightly wrapped in the film, and the remaining support is removed as the mouse is wrapped. (F) The mouse is successfully wrapped in the dressing, and its arms and legs are unconstrained.

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Materials

Name Company Catalog Number Comments
10% Neutral Buffered Formalin Fisher SF100-20 Fixative for histology
3M Vetbond Tissue Adhesive 3M 1469SB Surgical glue
Anti-GR1 clone RB6-8C5 BioXcell BE0075 Anti-rejection
Autoclave pouches VWR  89140-800 For autoclaving tools and paper towels
Buprenex 0.3 mg/mL Covetrus 59122 Analgesia
Carprofen 50 mg/mL Zoetis NADA # 141-199 Analgesia
D42 Dermatome blade Humeca 5.D42BL10 Dermatome (1 blade per sample)
Dermatome D42 Humeca 4.D42 Dermatome
Disposable Scalpel Bard-Parker 371610 skin preparation
Dissecting T-Pins; 1-1/2 inch, 1000/CS 1.5 Cole-Parmer UX-10915-03 To pin skin specimen for dermatome
Dissection scissors medicon 02.04.10 Sample preparation and mouse dissection
DNAse Sigma-Aldrich DN25-1G Skin digestion
Electric clippers Kent CL8787-KIT Hair removal
Forceps  medicon 07.60.07 Sample preparation and mouse dissection
Gauze Fisherbrand 22-362-178 Sample preparation
Heating lamp Morganville Scientific HL0100 Post-surgical care
Heating pads 4" x 10" Pristech 20415 Surgical heat supply
Insulin 1cc 12.7 mm syringes BD 329410 Drug administration
Isoflurane United States Pharmacopeia (USP)  NDC 66794-013-25 Anesthesia 
Isoflurane machine VetEquip 911103 Anesthesia
Nair for Men Nair ‎10022600588556 Hair removal
Neomycin and Polymyxin Bisulfates and Bacitracin Zinc Ophthalmic ointment Dechra  NDC 17478-235-35 Eye ointment to prevent drying
NOD.Cg-Prkdcscid Il2rgtm1Wjl/SzJ (NSG) mice The Jackson Laboratory 5557 Mice
Paper towels Kleenex 100848 May be autoclaved for sterile surfaces
Parafilm Fisher Scientific 13-374-12 Semitransparent sealing film
Petri Dish 150 mm Corning 430597 Sample storage
Plastic Wrap Fisherbrand 22-305-654 Site preparation
Providone-Iodine Swab stick PDI S41350 Site sterilization
Soft-Feed and Oral Hydration (Napa Nectar) Se Lab Group Inc NC9066511  For supplementing poorly recovering mice post-surgery
Specimen Collection Cups Fisher Scientific 22-150-266 Sample storage
Sterile alcohol prep pad Fisherbrand 22-363-750 Skin preparation
Sterile PBS Gibco 14190-144 Media for sample storage
Sterile saline Hospira NDC 0409-4888-02 For drug dilution
Tegaderm Film 4" x 43/4"  3M 1626 Transparent film wound dressing
Vaseline Petrolatum Gauze 3" x 8"  Kendall 414600 Wound dressing

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A Technique for Human Skin Grafting in a Mouse Model
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Source: Moss, M. I. et al., Xenograft Skin Model to Manipulate Human Immune Responses In Vivo. J. Vis. Exp. (2022)

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