MRC Human Genetics Unit, Institute of Genetics and Cancer, The University of Edinburgh, Western General Hospital Campus, Crewe Road, Edinburgh EH4 2XU, UK.
Cancer Research UK Scotland Centre, Institute of Genetics and Cancer, The University of Edinburgh, Western General Hospital Campus, Crewe Road, Edinburgh EH4 2XU, UK.
Development. 2022 May 15;149(10). doi: 10.1242/dev.200277. Epub 2022 May 19.
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.
斑马鱼中的黑素细胞干细胞 (McSCs) 在生长和再生过程中充当黑素细胞的按需来源,但与其激活和再生过程相关的代谢程序尚不清楚。在这里,我们使用活细胞成像与 scRNA-seq 相结合的方法发现,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 代谢开关以产生后代。出乎意料的是,尽管 ALDH2 以其清除醛的机制而闻名,但我们发现,在再生的 McSCs 中,Aldh2 活性通过甲醛代谢产生甲酸盐——核苷酸生物合成的一碳 (1C) 构建块——是必需的。因此,我们发现,用低剂量的甲氨蝶呤破坏 1C 循环会导致黑素细胞再生缺陷。在没有 Aldh2 的情况下,我们发现嘌呤是代谢终产物,足以使激活的 McSCs 产生后代。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 酶的反应产物具有组织特异性干细胞功能,可以满足再生中的代谢需求。