Aldh2 is a lineage-specific metabolic gatekeeper in melanocyte stem cells

Hannah Brunsdon, A. Brombin, Samuel J. Peterson, J. Postlethwait, E. Patton
{"title":"Aldh2 is a lineage-specific metabolic gatekeeper in melanocyte stem cells","authors":"Hannah Brunsdon, A. Brombin, Samuel J. Peterson, J. Postlethwait, E. Patton","doi":"10.1242/dev.200277","DOIUrl":null,"url":null,"abstract":"ABSTRACT Melanocyte stem cells (McSCs) in zebrafish serve as an on-demand source of melanocytes during growth and regeneration, but metabolic programs associated with their activation and regenerative processes are not well known. Here, using live imaging coupled with scRNA-sequencing, we discovered that, during regeneration, quiescent McSCs activate a dormant embryonic neural crest transcriptional program followed by an aldehyde dehydrogenase (Aldh) 2 metabolic switch to generate progeny. Unexpectedly, although ALDH2 is well known for its aldehyde-clearing mechanisms, we find that, in regenerating McSCs, Aldh2 activity is required to generate formate – the one-carbon (1C) building block for nucleotide biosynthesis – through formaldehyde metabolism. Consequently, we find that disrupting the 1C cycle with low doses of methotrexate causes melanocyte regeneration defects. In the absence of Aldh2, we find that purines are the metabolic end product sufficient for activated McSCs to generate progeny. Together, our work reveals McSCs undergo a two-step cell state transition during regeneration, and that the reaction products of Aldh2 enzymes have tissue-specific stem cell functions that meet metabolic demands in regeneration.","PeriodicalId":77105,"journal":{"name":"Development (Cambridge, England). Supplement","volume":"73 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-04-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Development (Cambridge, England). Supplement","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1242/dev.200277","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3

Abstract

ABSTRACT Melanocyte stem cells (McSCs) in zebrafish serve as an on-demand source of melanocytes during growth and regeneration, but metabolic programs associated with their activation and regenerative processes are not well known. Here, using live imaging coupled with scRNA-sequencing, we discovered that, during regeneration, quiescent McSCs activate a dormant embryonic neural crest transcriptional program followed by an aldehyde dehydrogenase (Aldh) 2 metabolic switch to generate progeny. Unexpectedly, although ALDH2 is well known for its aldehyde-clearing mechanisms, we find that, in regenerating McSCs, Aldh2 activity is required to generate formate – the one-carbon (1C) building block for nucleotide biosynthesis – through formaldehyde metabolism. Consequently, we find that disrupting the 1C cycle with low doses of methotrexate causes melanocyte regeneration defects. In the absence of Aldh2, we find that purines are the metabolic end product sufficient for activated McSCs to generate progeny. Together, our work reveals McSCs undergo a two-step cell state transition during regeneration, and that the reaction products of Aldh2 enzymes have tissue-specific stem cell functions that meet metabolic demands in regeneration.
Aldh2是黑素细胞干细胞谱系特异性代谢守门人
斑马鱼的黑素细胞干细胞(McSCs)在生长和再生过程中作为黑素细胞的按需来源,但与它们的激活和再生过程相关的代谢程序尚不清楚。在这里,利用实时成像和scrna测序,我们发现,在再生过程中,静止的McSCs激活休眠的胚胎神经嵴转录程序,随后是醛脱氢酶(Aldh) 2代谢开关来产生后代。出乎意料的是,尽管ALDH2以其醛清除机制而闻名,但我们发现,在再生McSCs中,ALDH2活性是通过甲醛代谢生成甲酸(核苷酸生物合成的一碳(1C)构建块)所必需的。因此,我们发现低剂量甲氨蝶呤破坏1C周期会导致黑素细胞再生缺陷。在缺乏Aldh2的情况下,我们发现嘌呤是足以激活McSCs产生后代的代谢终产物。总之,我们的工作揭示了McSCs在再生过程中经历了两步细胞状态转变,并且Aldh2酶的反应产物具有满足再生代谢需求的组织特异性干细胞功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信