Zhang Weidong, Wang Niu, Zhang Tongtong, Wang Meng, Ge Wei, Wang Xin
College of Animal Science and Technology, Northwest A&F University, Yangling, China.
College of Life Sciences, Qingdao Agricultural University, Qingdao, China.
Front Cell Dev Biol. 2021 Jun 4;9:686805. doi: 10.3389/fcell.2021.686805. eCollection 2021.
Emerging studies show that melatonin promotes cashmere development through hypodermic implantation. However, the impact and underlying mechanisms are currently unknown. study has previously demonstrated that melatonin induces cashmere growth by regulating the proliferation of goat secondary hair follicle stem cells (gsHFSCs), but there is limited information concerning the effects of melatonin on cell pluripotency. It is also known that Wnt signaling may actively participate in regulating cell proliferation and stem cell pluripotency. Therefore, in the current investigation, goat hair follicle stem cells were exposed to multiple concentrations of melatonin and different culture times to reveal the relationship between melatonin and the activation of Wnt signaling. A proportionally high Catenin beta-1 (CTNNB1) response was induced by 500 ng/L of melatonin, but it was then suppressed with the dosages over 1,000 ng/L. Greater amounts of CTNNB1 entered the cell nuclei by extending the exposure time to 72 h, which activated transcription factor 4/lymphoid enhancer-binding factor 1 and promoted the expression of the proliferation-related genes , , and . Moreover, nuclear receptor ROR-alpha (RORα) and bone morphogenetic protein 4 (BMP4) were employed to analyze the underlying mechanism. RORα presented a sluggish concentration/time-dependent rise, but BMP4 was increased dramatically by melatonin exposure, which revealed that melatonin might participate in regulating the pluripotency of hair follicle stem cells. Interestingly, NOGGIN, which is a BMP antagonist and highly relevant to cell stemness, was also stimulated by melatonin. These findings demonstrated that melatonin exposure and/or NOGGIN overexpression in hair follicle stem cells might promote the expression of pluripotency markers Homeobox protein NANOG, Organic cation/carnitine transporter 4, and Hematopoietic progenitor cell antigen CD34. Our findings here provided a comprehensive view of Wnt signaling in melatonin stimulated cells and melatonin mediated stemness of gsHFSCs by regulating NOGGIN, which demonstrates a regulatory mechanism of melatonin enhancement on the growth of cashmere.
新兴研究表明,褪黑素通过皮下植入促进羊绒生长。然而,其影响及潜在机制目前尚不清楚。此前有研究表明,褪黑素通过调节山羊次级毛囊干细胞(gsHFSCs)的增殖来诱导羊绒生长,但关于褪黑素对细胞多能性影响的信息有限。已知Wnt信号可能积极参与调节细胞增殖和干细胞多能性。因此,在当前研究中,将山羊毛囊干细胞暴露于多种浓度的褪黑素和不同培养时间,以揭示褪黑素与Wnt信号激活之间的关系。500 ng/L的褪黑素诱导了较高比例的β-连环蛋白1(CTNNB1)反应,但在剂量超过1000 ng/L时受到抑制。通过将暴露时间延长至72小时,更多的CTNNB1进入细胞核,激活了转录因子4/淋巴样增强因子1,并促进了增殖相关基因、和的表达。此外,采用核受体ROR-α(RORα)和骨形态发生蛋白4(BMP4)来分析潜在机制。RORα呈现出缓慢的浓度/时间依赖性升高,但褪黑素暴露使BMP4显著增加,这表明褪黑素可能参与调节毛囊干细胞的多能性。有趣的是,作为BMP拮抗剂且与细胞干性高度相关的NOGGIN也受到褪黑素的刺激。这些发现表明,毛囊干细胞中褪黑素暴露和/或NOGGIN过表达可能促进多能性标志物同源盒蛋白NANOG、有机阳离子/肉碱转运体4和造血祖细胞抗原CD34的表达。我们在此的发现提供了褪黑素刺激细胞中Wnt信号的全面视图,以及褪黑素通过调节NOGGIN介导gsHFSCs干性的情况,这揭示了褪黑素促进羊绒生长的调节机制。