Department of Dermatology, Qilu Hospital, Shandong University, Jinan, Shandong, 250012, China.
Laboratory of Basic Medical Science, Qilu Hospital, Shandong University, Jinan, Shandong, 250012, China.
Inflammation. 2024 Oct;47(5):1585-1599. doi: 10.1007/s10753-024-01995-7. Epub 2024 Mar 12.
Psoriasis is a chronic inflammatory skin disease characterized by abnormal keratinocyte proliferation and inflammation. MiRNAs and serum exosomes participate in the pathogenesis of many diseases. The objective of this study is to explore the function of miR-6785-5p in psoriatic keratinocytes and its upstream and downstream mechanisms. For our study, we employed qRT-PCR and fluorescence in situ hybridization to evaluate miR-6785-5p in psoriatic keratinocytes and conducted a microRNA microarray for identifying differentially expressed miRNAs in patient serum exosomes. We then cocultured keratinocytes with these exosomes, using immunofluorescence staining and qRT-PCR to assess uptake and miR-6785-5p overexpression. We explored miR-6785-5p's role through transfection with specific mimics and inhibitors and confirmed MNK2 as its target using a luciferase assay. MNK2's function was further examined using siRNA technology. Lastly, we applied an imiquimod-induced psoriasis mouse model, also employing siRNA, to investigate MNK2's role in psoriasis. MiR-6785-5p demonstrates a notable overexpression in the keratinocytes of psoriasis patients as well as in their serum exosomes. These keratinocytes actively uptake the miR-6785-5p-enriched serum exosomes. Functionally, miR-6785-5p appears to alleviate psoriasis-like skin damage, observable both in vitro and in vivo, by downregulating MNK2 expression. Psoriasis keratinocytes uptake serum exosomes highly expressing miR-6785-5p. MiR-6785-5p inhibits the abnormal proliferation and inflammatory state of keratinocytes by reducing MNK2 expression and interfering with the MNK2/p-eIF4E axis.
银屑病是一种慢性炎症性皮肤病,其特征为角质形成细胞异常增殖和炎症。miRNAs 和血清外泌体参与许多疾病的发病机制。本研究旨在探讨 miR-6785-5p 在银屑病角质形成细胞中的作用及其上下游机制。在我们的研究中,我们采用 qRT-PCR 和荧光原位杂交技术评估银屑病角质形成细胞中的 miR-6785-5p,并进行 miRNA 微阵列分析以鉴定患者血清外泌体中差异表达的 miRNAs。然后,我们将角质形成细胞与这些外泌体共培养,通过免疫荧光染色和 qRT-PCR 评估摄取和 miR-6785-5p 的过表达。我们通过转染特异性模拟物和抑制剂来探索 miR-6785-5p 的作用,并通过荧光素酶测定证实 MNK2 是其靶标。使用 siRNA 技术进一步研究了 MNK2 的功能。最后,我们应用咪喹莫特诱导的银屑病小鼠模型,同样使用 siRNA,研究 MNK2 在银屑病中的作用。miR-6785-5p 在银屑病患者的角质形成细胞及其血清外泌体中表现出明显的过表达。这些角质形成细胞主动摄取富含 miR-6785-5p 的血清外泌体。功能上,miR-6785-5p 通过下调 MNK2 表达,减轻银屑病样皮肤损伤,无论是在体外还是体内,都表现出明显的作用。银屑病角质形成细胞摄取高表达 miR-6785-5p 的血清外泌体。miR-6785-5p 通过减少 MNK2 表达并干扰 MNK2/p-eIF4E 轴来抑制角质形成细胞的异常增殖和炎症状态。