Mai Mori , Chie Kobori , Ryo Takagi , Moeka Tani , Hidenori Akutsu , Akihiro Umezawa
{"title":"控制黑素细胞密度的可重复性培养表皮片生产方法的建立","authors":"Mai Mori , Chie Kobori , Ryo Takagi , Moeka Tani , Hidenori Akutsu , Akihiro Umezawa","doi":"10.1016/j.reth.2025.04.001","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><div>Vitiligo, the most common human pigmentary disorder, significantly impacts patients' quality of life through its profound psychological and social consequences. The condition's complex pathogenesis and substantial effect on patients' well-being underscore the critical need for advanced therapeutic approaches. Treatment for vitiligo by autologous cultured epidermal transplantation has been developed, and the efficacy of this treatment has been determined. However, there is concern that differences in postoperative pigmentation of affected areas may occur due to difficulty in adjusting melanocyte content. This study aimed to develop a reproducible method for fabricating cultured epidermal sheets containing melanocytes for use in clinical applications.</div></div><div><h3>Methods</h3><div>Human epidermal keratinocytes and melanocytes derived from skin tissues of volunteer donors were prepared under different culture conditions and the proliferation of keratinocytes and melanocytes was determined. The density and percentage of melanocytes in cultured epidermal sheets were evaluated by DOPA staining and flow cytometry. Moreover, a novel clinical-grade melanocyte culture medium with specific supplements was developed that avoids bovine pituitary extract containing unknown animal-derived unknown materials.</div></div><div><h3>Results</h3><div>The density of melanocytes was higher when melanocytes were seeded first, as opposed to the simultaneous seeding of melanocytes and keratinocytes. The best condition in the present study for preparing cultured epidermal sheets with high melanocyte density was to seed melanocytes at 1.0 × 10<sup>4</sup> cells/cm<sup>2</sup> on Day 1, followed by feeder cells on Day 2 and keratinocytes at 8.0 × 10<sup>4</sup> cells/cm<sup>2</sup> on Day 3. The optimal culture medium for melanocytes was determined to contain 10 nM aMSH, 10 nM endothelin-1, and 10 μg/mL FGF-2 as culture supplements.</div></div><div><h3>Conclusions</h3><div>The results of this study establish a foundation for the development of cell therapy effective for vitiligo.</div></div>","PeriodicalId":20895,"journal":{"name":"Regenerative Therapy","volume":"29 ","pages":"Pages 499-505"},"PeriodicalIF":3.4000,"publicationDate":"2025-05-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Establishment of reproducible method for production of cultured epidermal sheets with controlled melanocyte density\",\"authors\":\"Mai Mori , Chie Kobori , Ryo Takagi , Moeka Tani , Hidenori Akutsu , Akihiro Umezawa\",\"doi\":\"10.1016/j.reth.2025.04.001\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Introduction</h3><div>Vitiligo, the most common human pigmentary disorder, significantly impacts patients' quality of life through its profound psychological and social consequences. The condition's complex pathogenesis and substantial effect on patients' well-being underscore the critical need for advanced therapeutic approaches. Treatment for vitiligo by autologous cultured epidermal transplantation has been developed, and the efficacy of this treatment has been determined. However, there is concern that differences in postoperative pigmentation of affected areas may occur due to difficulty in adjusting melanocyte content. This study aimed to develop a reproducible method for fabricating cultured epidermal sheets containing melanocytes for use in clinical applications.</div></div><div><h3>Methods</h3><div>Human epidermal keratinocytes and melanocytes derived from skin tissues of volunteer donors were prepared under different culture conditions and the proliferation of keratinocytes and melanocytes was determined. The density and percentage of melanocytes in cultured epidermal sheets were evaluated by DOPA staining and flow cytometry. Moreover, a novel clinical-grade melanocyte culture medium with specific supplements was developed that avoids bovine pituitary extract containing unknown animal-derived unknown materials.</div></div><div><h3>Results</h3><div>The density of melanocytes was higher when melanocytes were seeded first, as opposed to the simultaneous seeding of melanocytes and keratinocytes. The best condition in the present study for preparing cultured epidermal sheets with high melanocyte density was to seed melanocytes at 1.0 × 10<sup>4</sup> cells/cm<sup>2</sup> on Day 1, followed by feeder cells on Day 2 and keratinocytes at 8.0 × 10<sup>4</sup> cells/cm<sup>2</sup> on Day 3. The optimal culture medium for melanocytes was determined to contain 10 nM aMSH, 10 nM endothelin-1, and 10 μg/mL FGF-2 as culture supplements.</div></div><div><h3>Conclusions</h3><div>The results of this study establish a foundation for the development of cell therapy effective for vitiligo.</div></div>\",\"PeriodicalId\":20895,\"journal\":{\"name\":\"Regenerative Therapy\",\"volume\":\"29 \",\"pages\":\"Pages 499-505\"},\"PeriodicalIF\":3.4000,\"publicationDate\":\"2025-05-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Regenerative Therapy\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S235232042500077X\",\"RegionNum\":3,\"RegionCategory\":\"环境科学与生态学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CELL & TISSUE ENGINEERING\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Regenerative Therapy","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S235232042500077X","RegionNum":3,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CELL & TISSUE ENGINEERING","Score":null,"Total":0}
Establishment of reproducible method for production of cultured epidermal sheets with controlled melanocyte density
Introduction
Vitiligo, the most common human pigmentary disorder, significantly impacts patients' quality of life through its profound psychological and social consequences. The condition's complex pathogenesis and substantial effect on patients' well-being underscore the critical need for advanced therapeutic approaches. Treatment for vitiligo by autologous cultured epidermal transplantation has been developed, and the efficacy of this treatment has been determined. However, there is concern that differences in postoperative pigmentation of affected areas may occur due to difficulty in adjusting melanocyte content. This study aimed to develop a reproducible method for fabricating cultured epidermal sheets containing melanocytes for use in clinical applications.
Methods
Human epidermal keratinocytes and melanocytes derived from skin tissues of volunteer donors were prepared under different culture conditions and the proliferation of keratinocytes and melanocytes was determined. The density and percentage of melanocytes in cultured epidermal sheets were evaluated by DOPA staining and flow cytometry. Moreover, a novel clinical-grade melanocyte culture medium with specific supplements was developed that avoids bovine pituitary extract containing unknown animal-derived unknown materials.
Results
The density of melanocytes was higher when melanocytes were seeded first, as opposed to the simultaneous seeding of melanocytes and keratinocytes. The best condition in the present study for preparing cultured epidermal sheets with high melanocyte density was to seed melanocytes at 1.0 × 104 cells/cm2 on Day 1, followed by feeder cells on Day 2 and keratinocytes at 8.0 × 104 cells/cm2 on Day 3. The optimal culture medium for melanocytes was determined to contain 10 nM aMSH, 10 nM endothelin-1, and 10 μg/mL FGF-2 as culture supplements.
Conclusions
The results of this study establish a foundation for the development of cell therapy effective for vitiligo.
期刊介绍:
Regenerative Therapy is the official peer-reviewed online journal of the Japanese Society for Regenerative Medicine.
Regenerative Therapy is a multidisciplinary journal that publishes original articles and reviews of basic research, clinical translation, industrial development, and regulatory issues focusing on stem cell biology, tissue engineering, and regenerative medicine.