Department of Histology and Embryology, Guangzhou University of Chinese Medicine, Guangzhou, Guangdong 510006, P.R. China.
The Research Centre of Integrative Medicine, Guangzhou University of Chinese Medicine, Guangzhou, Guangdong 510006, P.R. China.
Mol Med Rep. 2018 Aug;18(2):1279-1286. doi: 10.3892/mmr.2018.9110. Epub 2018 May 31.
Our previous study indicated that loureirin A induces hair follicle stem cell (HFSC) differentiation through Wnt/β‑catenin signaling pathway activation. However, if and how microRNAs (miRNAs/miRs) modulate loureirin A‑induced differentiation remains to be elucidated. In the present study, HFSCs were separated from the vibrissae of rats and identified by CD34 and keratin, type 1 cytoskeletal (K)15 expression. Microarray‑based miRNA profiling analysis revealed that miR‑339‑5p was downregulated in loureirin A‑induced HFSC differentiation. miR‑339‑5p overexpression by transfection with miR‑339‑5p mimics markedly inhibited the expression of K10 and involucrin, which are markers of epidermal differentiation, whereas inhibition of miR‑339‑5p by miR‑339‑5p inhibitor transfection promoted the expression of K10 and involucrin. These results suggest that miR‑339‑5p is a negative regulator of HFSC differentiation following induction by loureirin A. These findings were confirmed by a luciferase assay. Homeobox protein DLX‑5 (DLX5) was identified as a direct target of miR‑339‑5p. Furthermore, it was demonstrated that miR‑339‑5p inhibited DLX5. Overexpression of miR‑339‑5p by mimic transfection significantly inhibited protein Wnt‑3a (Wnt3a) expression, while inhibition of miR‑339‑5p by inhibitor transfection significantly increased the expression of Wnt3a. Furthermore, small interfering RNA targeting DLX5 was transfected into HFSCs, and western blot analysis revealed that Wnt3a, involucrin and K10 expression was significantly downregulated. Taken together, these results suggest that miR‑339‑5p negatively regulated loureirin A‑induced HFSC differentiation by targeting DLX5, resulting in Wnt/β‑catenin signaling pathway inhibition. This may provide a possible therapeutic target for skin repair and regeneration.
我们之前的研究表明,芫花素 A 通过激活 Wnt/β-连环蛋白信号通路诱导毛囊干细胞(HFSC)分化。然而,miRNAs(miRs)是否以及如何调节芫花素 A 诱导的分化仍有待阐明。在本研究中,我们从大鼠胡须中分离出 HFSC,并通过 CD34 和角蛋白 15(K)表达进行鉴定。基于微阵列的 miRNA 谱分析显示,miR-339-5p 在芫花素 A 诱导的 HFSC 分化中下调。通过 miR-339-5p 模拟物转染过表达 miR-339-5p 可显著抑制角蛋白 10 和兜甲蛋白的表达,这是表皮分化的标志物,而通过 miR-339-5p 抑制剂转染抑制 miR-339-5p 则促进角蛋白 10 和兜甲蛋白的表达。这些结果表明,miR-339-5p 是芫花素 A 诱导 HFSC 分化后的负调控因子。这些发现通过荧光素酶报告基因实验得到了证实。同源盒蛋白 DLX-5(DLX5)被鉴定为 miR-339-5p 的直接靶标。此外,研究表明 miR-339-5p 抑制了 DLX5。通过 mimic 转染过表达 miR-339-5p 可显著抑制 Wnt-3a(Wnt3a)蛋白表达,而通过抑制剂转染抑制 miR-339-5p 则显著增加 Wnt3a 的表达。此外,将靶向 DLX5 的小干扰 RNA 转染到 HFSC 中,通过 Western blot 分析显示 Wnt3a、兜甲蛋白和角蛋白 10 的表达明显下调。综上所述,这些结果表明,miR-339-5p 通过靶向 DLX5 负调控芫花素 A 诱导的 HFSC 分化,从而抑制 Wnt/β-连环蛋白信号通路。这可能为皮肤修复和再生提供了一个潜在的治疗靶点。