iNOVA4Health, NOVA Medical School, Faculdade de Ciências Médicas, NMS, FCM, Universidade NOVA de Lisboa, 1169-056 Lisboa, Portugal.
Int J Mol Sci. 2023 Jul 10;24(14):11289. doi: 10.3390/ijms241411289.
Skin pigmentation ensures efficient photoprotection and relies on the pigment melanin, which is produced by epidermal melanocytes and transferred to surrounding keratinocytes. While the molecular mechanisms of melanin synthesis and transport in melanocytes are now well characterized, much less is known about melanin transfer and processing within keratinocytes. Over the past few decades, distinct models have been proposed to explain how melanin transfer occurs at the cellular and molecular levels. However, this remains a debated topic, as up to four different models have been proposed, with evidence presented supporting each. Here, we review the current knowledge on the regulation of melanin exocytosis, internalization, processing, and polarization. Regarding the different transfer models, we discuss how these might co-exist to regulate skin pigmentation under different conditions, i.e., constitutive and facultative skin pigmentation or physiological and pathological conditions. Moreover, we discuss recent evidence that sheds light on the regulation of melanin exocytosis by melanocytes and internalization by keratinocytes, as well as how melanin is stored within these cells in a compartment that we propose be named the melanokerasome. Finally, we review the state of the art on the molecular mechanisms that lead to melanokerasome positioning above the nuclei of keratinocytes, forming supranuclear caps that shield the nuclear DNA from UV radiation. Thus, we provide a comprehensive overview of the current knowledge on the molecular mechanisms regulating skin pigmentation, from melanin exocytosis by melanocytes and internalization by keratinocytes to processing and polarization within keratinocytes. A better knowledge of these molecular mechanisms will clarify long-lasting questions in the field that are crucial for the understanding of skin pigmentation and can shed light on fundamental aspects of organelle biology. Ultimately, this knowledge can lead to novel therapeutic strategies to treat hypo- or hyper-pigmentation disorders, which have a high socio-economic burden on patients and healthcare systems worldwide, as well as cosmetic applications.
皮肤色素沉着确保了有效的光保护,依赖于色素黑色素,它由表皮黑素细胞产生并转移到周围的角质形成细胞。虽然黑素细胞中黑色素合成和转运的分子机制现在已经很好地描述,但角质形成细胞中黑色素的转移和处理过程知之甚少。在过去的几十年中,已经提出了不同的模型来解释黑色素在细胞和分子水平上是如何转移的。然而,这仍然是一个有争议的话题,因为多达四种不同的模型已经被提出,每种模型都有证据支持。在这里,我们回顾了黑色素胞吐作用、内化、加工和极化的调控的最新知识。关于不同的转移模型,我们讨论了它们如何在不同的条件下共存,即组成性和 facultative 皮肤色素沉着或生理和病理条件,以调节皮肤色素沉着。此外,我们还讨论了最近的证据,这些证据阐明了黑素细胞中黑色素胞吐作用的调节和角质形成细胞中黑色素的内化,以及黑色素在这些细胞中如何储存在我们提议命名为黑素角质体的隔室中。最后,我们回顾了导致黑素角质体定位于角质形成细胞核上方,形成超核帽以保护核 DNA 免受 UV 辐射的分子机制的最新进展。因此,我们全面概述了调节皮肤色素沉着的分子机制的最新知识,从黑素细胞的黑色素胞吐作用和角质形成细胞的内化到角质形成细胞内的加工和极化。对这些分子机制的更好了解将澄清该领域长期存在的问题,这些问题对于理解皮肤色素沉着至关重要,并可以阐明细胞器生物学的基本方面。最终,这些知识可以为治疗色素减退或色素沉着障碍的新型治疗策略提供依据,色素减退或色素沉着障碍对全球患者和医疗保健系统造成了很高的社会经济负担,并且具有美容应用。