San Gallicano Dermatologic Institute, Rome, Italy.
Exp Dermatol. 2012 Jul;21(7):490-6. doi: 10.1111/j.1600-0625.2012.01506.x.
Understanding the cellular and molecular mechanisms leading to melanocyte loss in vitiligo is a mandatory step in improving the overall management of vitiligo patients. Until now, the study of vitiligo was characterised by a fragmented approach, and it is very hard to share and compare the data obtained by the different teams. The scenario mirrors the pathogenic puzzle, but it delays a true productive focus on the disease. The in vitro research is based on different models, ranging from monolayer cell culture of epidermal and dermal cells or 3D reconstructed skin to histological data, gene expression, computer simulation profile. For each model, several different (biochemical, phenotypic, immunological) aspects have been considered, increasing the mass of data difficult to be merged. Our purpose was to provide a practical synopsis of consolidated and advanced possibilities in the study of vitiligo, showing how data have been poorly shared until now. Following a short overview of the background of the disease, the approaches, ranging from basic cell biology to molecular and 'omics' studies, are summarised. New fluorescent probes and techniques open new possibilities for functional studies. Next, intracellular and superficial markers of the melanocytes, the main involved cells, are listed. Moving the focus from the epidermal level to the systemic and subcellular ones, this review aims to propose innovative multidisciplinary options for the vitiligo understanding. This paper focuses on the major practical and theoretical questions to be solved. It may be the basis for a more coordinated and productive approach to the biological question.
了解导致白癜风黑素细胞丧失的细胞和分子机制是改善白癜风患者整体管理的必要步骤。到目前为止,白癜风的研究一直采用碎片化的方法,不同团队获得的数据很难共享和比较。这种情况反映了发病机制的复杂性,但也阻碍了对该疾病的真正深入研究。体外研究基于不同的模型,从表皮和真皮细胞的单层细胞培养或 3D 重建皮肤到组织学数据、基因表达、计算机模拟等。对于每种模型,都考虑了几个不同的(生化、表型、免疫学)方面,增加了数据的数量,难以合并。我们的目的是提供一个关于白癜风研究中综合和先进的可能性的实用概述,展示迄今为止数据共享的不足之处。在简要概述疾病背景后,总结了从基础细胞生物学到分子和“组学”研究的方法。新型荧光探针和技术为功能研究开辟了新的可能性。接下来,列出了主要涉及细胞——黑素细胞的细胞内和表面标记物。将焦点从表皮水平转移到系统和亚细胞水平,本综述旨在为白癜风的理解提出创新的多学科选择。本文重点讨论了需要解决的主要实际和理论问题。它可能是对生物学问题进行更协调和富有成效的方法的基础。