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

Development

MRC Human Genetics Unit, Institute of Genetics and Cancer, The University of Edinburgh, Western General Hospital Campus, Crewe Road, Edinburgh EH4 2XU, UK.

Published: May 2022

AI Article Synopsis

  • McSCs in zebrafish are key for producing melanocytes during growth and repair, but their metabolic activation processes were unclear.
  • The study found that dormant McSCs activate a neural crest program and switch to an Aldh2 metabolism to produce necessary components for cell growth and regeneration.
  • Disruption of the one-carbon cycle impacted melanocyte regeneration, highlighting the importance of Aldh2 in providing metabolic support during this process.

Article 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9188749PMC
http://dx.doi.org/10.1242/dev.200277DOI Listing

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