UVB 照射的角质细胞衍生的外泌体 microRNAs 的综合分析作为潜在的黑色素生成调控因子。
Comprehensive Analysis of Exosomal MicroRNAs Derived from UVB-Irradiated Keratinocytes as Potential Melanogenesis Regulators.
机构信息
Department of Genetics and Biotechnology, Graduate School of Biotechnology, College of Life Science, Kyung Hee University, Yongin 446-701, Gyeonggi-do, Republic of Korea.
出版信息
Int J Mol Sci. 2024 Mar 7;25(6):3095. doi: 10.3390/ijms25063095.
The exosomes derived from keratinocytes can have a substantial impact on melanogenesis by influencing melanocytes. MicroRNAs (miRNAs) encapsulated within exosomes are implicated in the control of melanogenesis, particularly when under the influence of UVB irradiation. This investigation explores UVB-induced exosomal miRNAs from keratinocytes as potential regulators of melanogenesis. UVB-irradiated, keratinocyte-derived exosomes were observed to augment melanogenesis in melanocytes, resulting in an upregulation of MITF, TRP1, TRP2, and TYR expression compared to non-UVB-irradiated exosomes. Additionally, a subset of exosomal miRNAs was differentially selected and confirmed to exert both enhancing and inhibitory effects on melanogenesis through functional assays. Notably, hsa-miR-644a, hsa-miR-365b-5p, and hsa-miR-29c-3p were found to upregulate melanogenesis, while hsa-miR-18a-5p, hsa-miR-197-5p, and hsa-miR-4281 downregulated melanogenesis. These findings suggest the involvement of keratinocyte-derived exosomal miRNAs in melanogenesis regulation within melanocytes. The expression levels of exosomal miRNAs from keratinocytes exhibited a UVB-dependent increase, indicating a potential role for these miRNAs as regulators of melanogenesis in response to UVB irradiation. Furthermore, melanogenesis was found to be dependent on exosomes derived from keratinocytes. This underscores the potential of UVB-induced exosomal miRNAs derived from keratinocytes as regulators of melanogenesis. Moreover, this study unveils a significant role for exosomes in melanocyte pigmentation, presenting a novel pathway in the intricate process of melanogenesis.
角质细胞衍生的外泌体可以通过影响黑素细胞对黑色素生成产生重大影响。外泌体中包裹的 microRNAs(miRNAs)被认为参与黑色素生成的调控,尤其是在受到 UVB 照射的影响时。本研究探讨了角质细胞来源的 UVB 诱导的外泌体 miRNAs 是否可能作为黑色素生成的调节剂。与非 UVB 照射的外泌体相比,观察到 UVB 照射的角质细胞衍生的外泌体可增强黑素细胞中的黑色素生成,导致 MITF、TRP1、TRP2 和 TYR 的表达上调。此外,通过功能测定,发现一组外泌体 miRNAs 被差异选择并证实对黑色素生成具有增强和抑制作用。值得注意的是,hsa-miR-644a、hsa-miR-365b-5p 和 hsa-miR-29c-3p 被发现上调黑色素生成,而 hsa-miR-18a-5p、hsa-miR-197-5p 和 hsa-miR-4281 下调黑色素生成。这些发现表明角质细胞衍生的外泌体 miRNAs 参与了黑素细胞内黑色素生成的调控。角质细胞外泌体 miRNAs 的表达水平呈 UVB 依赖性增加,表明这些 miRNAs 作为黑色素生成的调节剂,可能对 UVB 照射产生反应。此外,黑色素生成依赖于角质细胞衍生的外泌体。这突显了 UVB 诱导的角质细胞衍生的外泌体 miRNAs 作为黑色素生成调节剂的潜力。此外,本研究揭示了外泌体在黑素细胞色素沉着中的重要作用,为黑色素生成这一复杂过程提供了一个新的途径。