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Transcriptome Analysis of Skin from SMP30/GNL Knockout Mice Reveals the Effect of Ascorbic Acid Deficiency on Skin and Hair

机译:SMP30 / GNL基因敲除小鼠皮肤的转录组分析揭示了抗坏血酸缺乏症对皮肤和头发的影响

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Background/Aim: Senescence marker protein-30/gluconolactonase knockout mice (SMP-30/GNL-KO) are a very useful model for clarifying the involvement of vitamin C (VC) in aging-related diseases. In this study, the effects of VC deficiency on skin and hair growth were investigated using SMP-30/GNL-KO mice by RNA sequencing. Materials and Methods: SMP-30/GNL-KO mice were given water containing 1.5 g/l VC until up to 8 weeks after birth to maintain a VC concentration in their organs and plasma equivalent to that in wild-type mice. The mice were then divided into two groups: a VC(+) group, where VC was administered, and a VC(-) group, where VC was not administered. Skin samples were collected at 4 and 8 weeks after the treatment. RNA was extracted from each skin sample, followed by cDNA synthesis and RNA-seq. In addition, hair growth was compared between the VC(-) and VC(+) groups after shaving. Skin samples were collected from the shaved area for histological examination by hematoxylin & eosin (HE) staining. Results: RNA-seq revealed that there were 1,736 (FDR<0.001) differentially expressed genes in the VC(-) and VC(+) groups. From the functional analysis of the differentially expressed genes in the VC(-) and VC(+) groups, predicted functionalities including cell death and cytotoxicity increased in the VC(+) group. Furthermore, it was predicted that the difference in hair growth between the VC(-) and VC(+) groups was caused by the expression of genes including keratin-related genes and the Sonic hedgehog gene. It was confirmed that hair growth was significantly promoted; hair growth from hair papilla cells was also confirmed by HE staining of the shaved backs of SMP-30/GNL-KO mice in the VC(+) group. Conclusion: RNA-seq of the skin from VC-deficient mice showed the effects of VC deficiency on the expression of genes involved in cell growth and the hair cycle. Visual inspection suggested that changes in the expression of the genes are involved in delaying hair growth in the VC(-) group. Further research on the relationship among VC deficiency, the hair cycle, and skin cell growth may contribute to research on hair restoration and skin aging.
机译:背景/目的:衰老标志物蛋白30 /葡萄糖酸内酯酶敲除小鼠(SMP-30 / GNL-KO)是一个非常有用的模型,用于阐明维生素C(VC)与衰老相关的疾病。在这项研究中,使用SMP-30 / GNL-KO小鼠通过RNA测序研究了VC缺乏对皮肤和头发生长的影响。材料和方法:给予SMP-30 / GNL-KO小鼠水1.5 g / l VC,直至出生后8周,以使其器官和血浆中的VC浓度保持与野生型小鼠相同。然后将小鼠分为两组:VC(+)组,其中施用VC;和VC(-)组,其中不施用VC。在治疗后第4和第8周收集皮肤样品。从每个皮肤样品中提取RNA,然后进行cDNA合成和RNA-seq。此外,比较了剃须后VC(-)和VC(+)组之间的毛发生长。从剃毛区域收集皮肤样品,以通过苏木精和曙红(HE)染色进行组织学检查。结果:RNA-seq显示VC(-)和VC(+)组中有1,736个(FDR <0.001)差异表达基因。通过对VC(-)和VC(+)组中差异表达基因的功能分析,预测的功能(包括细胞死亡和细胞毒性)在VC(+)组中有所增加。此外,据预测,VC(-)和VC(+)组之间的毛发生长的差异是由包括角蛋白相关基因和Sonic猬蛋白基因在内的基因表达引起的。可以确认的是,毛发生长得到明显促进。 VC(+)组中SMP-30 / GNL-KO小鼠剃毛后背的HE染色也证实了毛发乳头细胞的毛发生长。结论:VC缺陷小鼠皮肤的RNA序列显示VC缺陷对参与细胞生长和毛发周期的基因表达的影响。视觉检查表明,在VC(-)组中,基因表达的变化与头发的生长延迟有关。进一步研究VC缺乏,头发周期和皮肤细胞生长之间的关系可能有助于头发恢复和皮肤衰老的研究。

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