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Aged hematopoietic stem cells (HSCs) display diminished self-renewal and a myeloid differentiation bias. However, the drivers and mechanisms that underpin this fundamental switch are not understood. HSCs produce genotoxic formaldehyde that requires protection by the detoxification enzymes ALDH2 and ADH5 and the Fanconi anemia (FA) DNA repair pathway. We find that the HSCs in young Aldh2-/-Fancd2-/- mice harbor a transcriptomic signature equivalent to aged wild-type HSCs, along with increased epigenetic age, telomere attrition, and myeloid-biased differentiation quantified by single HSC transplantation. In addition, the p53 response is vigorously activated in Aldh2-/-Fancd2-/- HSCs, while p53 deletion rescued this aged HSC phenotype. To further define the origins of the myeloid differentiation bias, we use a GFP genetic reporter to find a striking enrichment of Vwf+ myeloid and megakaryocyte-lineage-biased HSCs. These results indicate that metabolism-derived formaldehyde-DNA damage stimulates the p53 response in HSCs to drive accelerated aging.

Original publication

DOI

10.1016/j.molcel.2023.05.035

Type

Journal article

Journal

Mol Cell

Publication Date

20/07/2023

Volume

83

Pages

2417 - 2433.e7

Keywords

DNA damage, DNA-damage response, aging, aldehydes, hematopoiesis, myeloid bias, p53, Animals, Mice, Aging, Hematopoiesis, Tumor Suppressor Protein p53, DNA Damage, Aldehydes, Transcriptome, Single-Cell Gene Expression Analysis, Hematopoietic Stem Cells, Myeloid Cells, Humans, Leukemia, Myeloid, Acute