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Yoshizato T, Nilsson C, Grasso F, Högstrand K, Mazzi S, Winroth A, Lehander M, Barbosa I, Waldin G, Mortera-Blanco T, Jansson M, Widfeldt MH, Aliouat A, Brennan MS, Markljung E, Hillen A, Chari E, Hellström-Lindberg E, Kretzschmar WW, Woll PS, Jacobsen SEW
Nat. Genet. - (-) - [2025-11-11; online 2025-11-11]
Dynamic steady-state lineage contribution of human hematopoietic stem cell (HSC) clones needs to be assessed over time. However, clonal contribution of HSCs has only been investigated at single time points and without assessing the critical erythroid and platelet lineages. Here we screened for somatic mutations in healthy aged individuals, identifying expanded HSC clones accessible for lineage tracing of all major blood cell lineages. In addition to HSC clones with balanced contribution to all lineages, we identified clones with all myeloid lineages but no or few B and T lymphocytes or all myeloid lineages and B cells but no T cells. No other lineage restriction patterns were reproducibly observed. Retrospective phylogenetic inferences uncovered a 'hierarchical' pattern of descendant subclones more lineage biased than their ancestral clone and a more common 'stable' pattern with descendant subclones showing highly concordant lineage contributions with their ancestral clone, despite decades of separation. Prospective lineage tracing confirmed remarkable stability over years of HSC clones with distinct lineage replenishment patterns.
NGI Stockholm (Genomics Production) [Service]
National Genomics Infrastructure [Service]
PubMed 41219528
DOI 10.1038/s41588-025-02405-w
Crossref 10.1038/s41588-025-02405-w
pii: 10.1038/s41588-025-02405-w