College of Animal Science and Technology, Yangzhou University, Yangzhou 225009, China.
Joint International Research Laboratory of Agriculture and Agri-Product Safety of Ministry of Education of China, Yangzhou University, Yangzhou 225009, China.
Int J Mol Sci. 2024 Jul 20;25(14):7950. doi: 10.3390/ijms25147950.
Wool is generated by hair follicles (HFs), which are crucial in defining the length, diameter, and morphology of wool fibers. However, the regulatory mechanism of HF growth and development remains largely unknown. Dermal papilla cells (DPCs) are a specialized cell type within HFs that play a crucial role in governing the growth and development of HFs. This study aims to investigate the proliferation and induction ability of ovine DPCs to enhance our understanding of the potential regulatory mechanisms underlying ovine HF growth and development. Previous research has demonstrated that microRNA-181a (miR-181a) was differentially expressed in skin tissues with different wool phenotypes, which indicated that miR-181a might play a crucial role in wool morphogenesis. In this study, we revealed that miR-181a inhibited the proliferation and induction ability of ovine DPCs by quantitative Real-time PCR (qRT-PCR), cell counting Kit-8 (CCK-8), 5-ethynyl-2'-deoxyuridine (EdU), flow cytometry, and alkaline phosphatase staining. Then, we also confirmed G protein subunit alpha i2 () is a target gene of miR-181a by dual luciferase reporter assay, qRT-PCR, and Western blot, and that it could promote the proliferation and induction ability of ovine DPCs. In addition, could also activate the Wnt/β-Catenin signaling pathway in ovine DPCs. This study showed that miR-181a can inhibit the proliferation and induction ability of ovine DPCs by targeting through the Wnt/β-Catenin signaling pathway.
羊毛由毛囊(HFs)产生,毛囊对于确定羊毛纤维的长度、直径和形态至关重要。然而,HF 生长和发育的调控机制在很大程度上仍然未知。真皮乳头细胞(DPCs)是 HFs 中的一种特化细胞类型,在调控 HFs 的生长和发育中起着关键作用。本研究旨在探讨绵羊 DPCs 的增殖和诱导能力,以增强我们对绵羊 HF 生长和发育潜在调控机制的理解。先前的研究表明,microRNA-181a(miR-181a)在具有不同羊毛表型的皮肤组织中差异表达,这表明 miR-181a 可能在羊毛形态发生中发挥重要作用。在本研究中,我们通过定量实时 PCR(qRT-PCR)、细胞计数试剂盒-8(CCK-8)、5-乙炔基-2'-脱氧尿苷(EdU)、流式细胞术和碱性磷酸酶染色发现,miR-181a 抑制绵羊 DPCs 的增殖和诱导能力。然后,我们还通过双荧光素酶报告基因检测、qRT-PCR 和 Western blot 证实 G 蛋白亚单位α i2()是 miR-181a 的靶基因,并且它可以促进绵羊 DPCs 的增殖和诱导能力。此外,还可以激活绵羊 DPCs 中的 Wnt/β-Catenin 信号通路。本研究表明,miR-181a 可以通过靶向 Wnt/β-Catenin 信号通路抑制绵羊 DPCs 的增殖和诱导能力。