A kinetics-based model of haematopoiesis reveals extrinsic regulation of skewed lineage output from stem cells
Authors
- Esther Rodríguez-Correa
- Florian Grünschläger
- Tamar Nizharadze
- Natasha Anstee
- Jude Al-Sabah
- Vojtech Kumpost
- Anastasia Sedlmeier
- Congxin Li
- Melanie Ball
- Foteini Fotopoulou
- Jeyan Jayarajan
- Ian Ghezzi
- Julia Knoch
- Megan Druce
- Kleo Aurich
- Marleen Büchler-Schäff
- Susanne Lux
- Pablo Hernández-Malmierca
- Julius Gräsel
- Dominik Vonficht
- Marta López-Osias
- Elvira González-Saiz
- Daniel Fernández-Pérez
- Anna Mathioudaki
- Judith Zaugg
- Alejo Rodríguez-Fraticelli
- Ralf Mikut
- Andreas Trumpp
- Thomas Höfer
- Daniel Hübschmann
- Simon Haas
- Michael D. Milsom
Journal
- Nature Cell Biology
Citation
- Nat Cell Biol
Abstract
Haematopoietic stem cells (HSCs) display extensive molecular and functional heterogeneity. However, a cohesive model that explains the relationship and biological relevance of these diverse HSC states remains elusive. Here, by performing single-cell transplantations of over 1,000 highly purified murine long-term HSCs combined with in-depth phenotyping of their clonal progeny, we define kinetics-based reconstitution parameters which aligned HSCs into a single hierarchical trajectory reflective of functional potency. This approach revealed that previously identified lineage biases are actually transitory states along this linear trajectory, not a discrete stable condition. Single-cell secondary transplantations validated hierarchical ordering based on reconstitution kinetics, whereas mathematical modelling combined with experimental modulation of lineage-biased blood production revealed that apparent lineage-biased outputs actually arise from cell-extrinsic feedback regulation and clonal competition between slow- and fast-engrafting clones to fill mature lineages to their compartment size limit. This study reconciles multiple layers of HSC heterogeneity into a unifying framework.