Pimecrolimus increases the melanogenesis and migration of melanocytes in vitro.
10.4196/kjpp.2017.21.3.287
- Author:
Ping XU
1
;
Jie CHEN
;
Cheng TAN
;
Ren Sheng LAI
;
Zhong Sheng MIN
Author Information
1. First Clinical College, Nanjing University of Chinese Medicine, Nanjing 210029, China. tancheng@medmail.com.cn
- Publication Type:Original Article
- Keywords:
Calcineurin;
Melanogenesis;
Migration;
Pimecrolimus;
Vitiligo
- MeSH:
Calcineurin;
Calcineurin Inhibitors;
Collagen;
Emigration and Immigration;
Hair Follicle;
In Vitro Techniques*;
Melanins;
Melanocytes*;
Microphthalmia-Associated Transcription Factor;
Monophenol Monooxygenase;
Tacrolimus;
Vitiligo;
Wounds and Injuries
- From:The Korean Journal of Physiology and Pharmacology
2017;21(3):287-292
- CountryRepublic of Korea
- Language:English
-
Abstract:
Vitiligo is an intriguing depigmentary disorder and is notoriously difficult to be treated. The ultimate goal of vitiligo treatment is to replenish the lost melanocytes by immigration from hair follicle and to restore the normal function of melanogenesis by residual melanocytes. There are two types of topical calcineurin inhibitors called tacrolimus and pimecrolimus, and are recommended as the first-line treatments in vitiligo. Although pimecrolimus is efficacious for the repigmentation of vitiligo, its intrinsic mechanisms have never been investigated in vitro. This research aimed to study the ability of pimecrolimus on stimulating melanogenesis, melanocyte migration and MITF (microphthalmia associated transcription factor) protein expression. Results showed that pimecrolimus at the dosages of 1, 10, 10² nM were neither mitogenic nor cytotoxic to melanocytes. The addition of pimecrolimus at 10, 10² and 10³ nM significantly increased intracellular tyrosinase activity, which was consistent with the elevated content of melanin content at the same concentrations. The peak effect was seen at 72 h in response to 10² nM pimecrolimus. Results of the wound scratch assay and Transwell assays indicate that pimecrolimus is effective in facilitating melanocyte migration on a collagen IV-coated surface. In addition, MITF protein yield reached the highest by pimecrolimus at 10² nM. In brief, pimecrolimus enhances melanin synthesis as well as promotes migration of melanocytes directly, possibly via their effects on MITF protein expression.
