Li Sijing, Chik Zamri, Faruqu Farid Nazer, Mohd Hashim Najihah, Mohd Yusof Nor Saadah, Fernandez Alarcon Jennifer, Ahmad Noraini
Department of Chemistry, Faculty of Science, Universiti Malaya, Kuala Lumpur, Malaysia.
Department of Biomedical Engineering, School of Engineering, Dali University, Dali, Yunnan, China.
Front Cell Dev Biol. 2025 Jul 18;13:1608902. doi: 10.3389/fcell.2025.1608902. eCollection 2025.
Psoriasis is a chronic inflammatory skin disorder characterized by hyperproliferation of keratinocytes, immune dysregulation, and abnormal epidermal differentiation. Its pathogenesis involves complex interactions among keratinocytes, fibroblasts, T cells, and myeloid cells, where dynamic cytoskeletal and extracellular matrix changes critically mediate intercellular communication. Emerging evidence highlights the pivotal roles of miRNAs and exosomes in coordinating these processes: miRNAs regulate cytoskeletal organization and extracellular matrix composition, while exosomes act as intercellular messengers that deliver miRNA-mediated signals, collectively shaping cell behavior and disease progression. This review synthesizes current knowledge on how miRNA-exosome networks drive cytoskeleton-extracellular matrix crosstalk in psoriasis, emphasizing their implications for cellular communication and tissue remodeling. By elucidating these mechanisms, we identify potential therapeutic opportunities to target pathogenic signaling pathways, offering new strategies for psoriasis management.
银屑病是一种慢性炎症性皮肤病,其特征为角质形成细胞过度增殖、免疫失调和表皮分化异常。其发病机制涉及角质形成细胞、成纤维细胞、T细胞和髓样细胞之间的复杂相互作用,其中动态的细胞骨架和细胞外基质变化在细胞间通讯中起关键介导作用。新出现的证据突显了微小RNA(miRNA)和外泌体在协调这些过程中的关键作用:miRNA调节细胞骨架组织和细胞外基质组成,而外泌体作为细胞间信使传递miRNA介导的信号,共同塑造细胞行为和疾病进展。本综述综合了关于miRNA-外泌体网络如何驱动银屑病中细胞骨架-细胞外基质相互作用的现有知识,强调它们对细胞通讯和组织重塑的影响。通过阐明这些机制,我们确定了针对致病信号通路的潜在治疗机会,为银屑病管理提供了新策略。