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脂肪量与肥胖相关基因通过N6-甲基腺苷修饰小眼相关转录因子对毛囊来源的神经嵴干细胞向黑素细胞分化的抑制作用

The Suppression Effects of Fat Mass and Obesity Associated Gene on the Hair Follicle-Derived Neural Crest Stem Cells Differentiating into Melanocyte by N6-Methyladenosine Modifying Microphthalmia-Associated Transcription Factor.

作者信息

Shang Zhiwei, Feng Haixia, Xia Liye

机构信息

Department of Dermatology, The First Affiliated Hospital, College of Clinical Medicine of Henan University of Science and Technology, Luoyang, China.

出版信息

Int J Stem Cells. 2023 May 30;16(2):135-144. doi: 10.15283/ijsc22106. Epub 2023 Feb 28.

Abstract

BACKGROUND AND OBJECTIVES

Melanocyte (MC), derived from neural crest stem cell (NCSC), are involved in the production of melanin. The mechanism by which NCSC differentiates to MC remains unclear. N6-methyladenosine (m6A) modification was applied to discuss the potential mechanism.

METHODS AND RESULTS

NCSCs were isolated from hair follicles of rats, and were obtained for differentiation. Cell viability, tyrosinase secretion and activity, and transcription factors were combined to evaluated the MC differentiation. RT-qPCR was applied to determine mRNA levels, and western blot were used for protein expression detection. Total m6A level was measured using methylated RNA immunoprecipitation (MeRIP) assay, and RNA immunoprecipitation was used to access the protein binding relationship. In current work, NCSCs were successfully differentiated into MCs. Fat mass and obesity associated gene (FTO) was aberrant downregulated in MCs, and elevated FTO suppressed the differentiation progress of NCSCs into MCs. Furthermore, microphthalmia-associated transcription factor (Mitf), a key gene involved in MC synthesis, was enriched by FTO in a m6A modification manner and degraded by FTO. Meanwhile, the suppression functions of FTO in the differentiation of NCSCs into MCs were reversed by elevated Mitf.

CONCLUSIONS

In short, FTO suppressed the differentiating ability of hair follicle-derived NCSCs into MCs by m6A modifying Mitf.

摘要

背景与目的

黑素细胞(MC)起源于神经嵴干细胞(NCSC),参与黑色素的生成。NCSC向MC分化的机制尚不清楚。本研究应用N6-甲基腺苷(m6A)修饰来探讨其潜在机制。

方法与结果

从大鼠毛囊中分离出NCSC并诱导其分化。结合细胞活力、酪氨酸酶分泌与活性以及转录因子来评估MC的分化情况。采用RT-qPCR检测mRNA水平,western blot检测蛋白表达。使用甲基化RNA免疫沉淀(MeRIP)试验检测总m6A水平,并通过RNA免疫沉淀分析蛋白结合关系。在本研究中,NCSC成功分化为MC。脂肪量和肥胖相关基因(FTO)在MC中异常下调,上调FTO可抑制NCSC向MC的分化进程。此外,小眼相关转录因子(Mitf)作为参与MC合成的关键基因,被FTO以m6A修饰的方式富集并降解。同时,上调Mitf可逆转FTO对NCSC向MC分化的抑制作用。

结论

简而言之,FTO通过对Mitf进行m6A修饰抑制毛囊来源的NCSC向MC的分化能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e094/10226864/d346cb4ee7df/ijsc-16-2-135-f1.jpg

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