Department of Toxicology, School of Public Health, Jilin University, Changchun, China; Department of Pathology, Xiang'an Hospital Of Xiamen University, Xiamen, China.
Department of Toxicology, School of Public Health, Jilin University, Changchun, China.
Pathol Res Pract. 2020 Nov;216(11):153224. doi: 10.1016/j.prp.2020.153224. Epub 2020 Sep 28.
Melanocytes are the major cells responsible for skin and fair pigmentation in vertebrates. They localize to hair follicles(HFs) and the epidermis during embryonic development. A reduced number or dysfunction of melanocytes results in pigmentation disorders.Thus, methods for isolation, culture, and identification of melanocytes in mouse hair follicles provide an experimental basis for thestudy of of pigmentation disorders. In the current work, we harvested the melanocytes from the anagen phase dorsal skin of C57BL/6 mice.After its separation from the skin, the dermis was digested, and the HFs were released. HFs were then also digested, and the cells released from HFs were cultured in melanocyte growth medium. Immunofluorescence and immunohistochemistry staining were used to localize the distribution of melanocytes in HFs . Reverse transcription polymerase chain reaction was performed to detect the expression of specific melanocyte marker genes. Immunofluorescence, immunohistochemistry, flow cytometry, and western blot were carried out to detect the expression of marker proteins in cells. 3,4-Dihydroxy-L-phenylalanine (L-DOPA) staining was used to detect the pigmentation functionality of melaonocytes. Based on our results, we conclude that mature and functional melanocytes can be successfully obtained from theHFs, providing a cell model to study pigmentation disorders. The current findings provide novel insights for the treatment of pigmentation disorders by autologous cell transplantation. Further, we believe that issues related to skin damage, insufficient numbers of autologous cells, and autoimmune problems can be resolved in future though the use of functional melanocytes.
黑素细胞是脊椎动物皮肤和浅色色素沉着的主要细胞。它们在胚胎发育过程中定位于毛囊 (HFs) 和表皮。黑素细胞数量减少或功能障碍会导致色素沉着紊乱。因此,分离、培养和鉴定小鼠毛囊黑素细胞的方法为色素沉着紊乱的研究提供了实验基础。在本工作中,我们从 C57BL/6 小鼠生长期背部皮肤中收获黑素细胞。从皮肤分离后,真皮被消化,毛囊被释放。然后也消化毛囊,从毛囊中释放的细胞在黑素细胞生长培养基中培养。免疫荧光和免疫组织化学染色用于定位毛囊中黑素细胞的分布。通过反转录聚合酶链反应检测特定黑素细胞标记基因的表达。通过免疫荧光、免疫组织化学、流式细胞术和 Western blot 检测细胞中标记蛋白的表达。3,4-二羟基-L-苯丙氨酸 (L-DOPA) 染色用于检测黑素细胞的色素形成功能。根据我们的结果,我们得出结论,从 HFs 中可以成功获得成熟和功能正常的黑素细胞,为研究色素沉着紊乱提供了细胞模型。目前的研究结果为通过自体细胞移植治疗色素沉着紊乱提供了新的思路。此外,我们相信通过使用功能正常的黑素细胞,未来可以解决与皮肤损伤、自体细胞数量不足和自身免疫问题相关的问题。