CEDOC, Faculdade de Ciências Médicas, Universidade Nova de Lisboa, Lisboa, Portugal; Instituto Gulbenkian de Ciência, Oeiras, Portugal; Molecular Medicine, National Heart and Lung Institute, Imperial College London, London, UK.
Molecular Medicine, National Heart and Lung Institute, Imperial College London, London, UK.
J Invest Dermatol. 2014 Apr;134(4):1056-1066. doi: 10.1038/jid.2013.432. Epub 2013 Oct 18.
The transfer of melanin from melanocytes to keratinocytes is a crucial process underlying maintenance of skin pigmentation and photoprotection against UV damage. Here, we present evidence supporting coupled exocytosis of the melanin core, or melanocore, by melanocytes and subsequent endocytosis by keratinocytes as a predominant mechanism of melanin transfer. Electron microscopy analysis of human skin samples revealed three lines of evidence supporting this: (1) the presence of melanocores in the extracellular space; (2) within keratinocytes, melanin was surrounded by a single membrane; and (3) this membrane lacked the melanosomal membrane protein tyrosinase-related protein 1 (TYRP1). Moreover, co-culture of melanocytes and keratinocytes suggests that melanin exocytosis is specifically induced by keratinocytes. Furthermore, depletion of Rab11b, but not Rab27a, caused a marked decrease in both keratinocyte-stimulated melanin exocytosis and transfer to keratinocytes. Thus, we propose that the predominant mechanism of melanin transfer is keratinocyte-induced exocytosis, mediated by Rab11b through remodeling of the melanosome membrane, followed by subsequent endocytosis by keratinocytes.
黑色素从黑素细胞向角质形成细胞的转移是维持皮肤色素沉着和防止紫外线损伤的关键过程。在这里,我们提出了支持黑素体(melanocore)由黑素细胞偶联胞吐作用,随后被角质形成细胞内吞的证据,这是黑色素转移的主要机制。对人皮肤样本的电子显微镜分析提供了三条支持这一观点的证据:(1)黑素体存在于细胞外空间;(2)在角质形成细胞内,黑色素被单层膜包围;(3)该膜缺乏黑素体膜蛋白酪氨酸酶相关蛋白 1(TYRP1)。此外,黑素细胞和角质形成细胞的共培养表明,黑色素的胞吐作用是由角质形成细胞特异性诱导的。此外,Rab11b 的耗竭而不是 Rab27a 的耗竭导致角质形成细胞刺激的黑色素胞吐作用和向角质形成细胞的转移明显减少。因此,我们提出黑色素转移的主要机制是由 Rab11b 通过重塑黑素体膜介导的角质形成细胞诱导的胞吐作用,随后被角质形成细胞内吞。