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LETTERS
6 (
2
); 126-126
doi:
10.4103/0974-2077.112680

Epidermal Cell Suspension: Achieved by Incubation at Room Temperature

Department of Dermatology and Skin Science, University of British Columbia, Vancouver, British Columbia, Canada
National Center for Vitiligo and Psoriasis, Riyadh, Saudi Arabia

Address for correspondence: Smita S Mulekar, National Center for Vitiligo and Psoriasis, Riyadh, Saudi Arabia. E-mail: mulekar@gmail.com

Licence

This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Disclaimer:
This article was originally published by Medknow Publications & Media Pvt Ltd and was migrated to Scientific Scholar after the change of Publisher.

Sir,

Non-cultured autologous melanocyte transplantation is one of the surgical treatments commonly used to treat clinically stable vitiligo patients. It involves a series of steps that has been described in previous publications.[1] One of the steps involves transferring a thin skin shave biopsy sample from the thigh to a petri dish containing 0.2% w/v trypsin solution. This is typically followed by incubation at 37°C using an incubator for 50 min. This is thought to be important for trypsin activation and subsequent separation of the epidermis from the dermis. We conducted an experiment to check the possibility of separating the epidermis from the dermis at room temperature (RT) without the need to use an incubator.

One of the authors (Mohammed I. AlJasser) volunteered to undergo the procedure. Two thin shave biopsy samples were obtained from the right thigh under local anesthesia. Both specimens were transferred to a petri dish containing 0.2% w/v trypsin solution. One specimen was incubated at 37°C using an incubator and the other was incubated at RT in an air-conditioned room. After 50 min, we were able to separate the epidermis from the dermis in both specimens [Figure 1]. The final prepared melanocyte suspension was of similar quality [Figure 2].

Separation process. The dermis (top) was separated from the epidermis (bottom) in both specimens. RT: Room temperature
Figure 1
Separation process. The dermis (top) was separated from the epidermis (bottom) in both specimens. RT: Room temperature
Final prepared melanocyte suspension with a similar quality in both specimens
Figure 2
Final prepared melanocyte suspension with a similar quality in both specimens

This simple experiment shows that the use of an incubator may not be necessary to separate the dermis from epidermis in order to prepare epidermal cell suspension. The concept has been supported by Vielkind and Crawford who demonstrated trypsinization of epithelium under various conditions.[2] This helps to simplify the melanocyte-keratinocyte transplantation procedure; thus, making it simpler by eliminating the use of an incubator. Further studies in a larger sample size are required to validate this finding.

REFERENCES

  1. , . Long-term follow-up study of 142 patients with vitiligo vulgaris treated by autologous, non-cultured melanocyte-keratinocyte cell transplantation. Int J Dermatol. 2005;44:841-5.
    [Google Scholar]
  2. , , . Evaluation of different procedures for the dissociation of retinal pigmented epithelium into single viable cells. Pigment Cell Res. 1988;1:419-33.
    [Google Scholar]

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