Author
Listed:
- Bong Ihn Koh
(Max Planck Institute for Molecular Biomedicine)
- Vishal Mohanakrishnan
(Max Planck Institute for Molecular Biomedicine)
- Hyun-Woo Jeong
(Max Planck Institute for Molecular Biomedicine)
- Hongryeol Park
(Max Planck Institute for Molecular Biomedicine)
- Kai Kruse
(Max Planck Institute for Molecular Biomedicine)
- Young Jun Choi
(University of Ulsan College of Medicine)
- Melina Nieminen-Kelhä
(Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin)
- Rahul Kumar
(University Medicine Mainz)
- Raquel S. Pereira
(Georg-Speyer-Haus Institute for Tumor Biology and Experimental Medicine and Goethe University Frankfurt)
- Susanne Adams
(Max Planck Institute for Molecular Biomedicine)
- Hyuek Jong Lee
(Institute for Basic Science)
- M. Gabriele Bixel
(Max Planck Institute for Molecular Biomedicine)
- Peter Vajkoczy
(Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin)
- Daniela S. Krause
(University Medicine Mainz)
- Ralf H. Adams
(Max Planck Institute for Molecular Biomedicine)
Abstract
The bone marrow microenvironment is a critical regulator of haematopoietic stem cell self-renewal and fate1. Although it is appreciated that ageing, chronic inflammation and other insults compromise bone marrow function and thereby negatively affect haematopoiesis2, it is not known whether different bone compartments exhibit distinct microenvironmental properties and functional resilience. Here we use imaging, pharmacological approaches and mouse genetics to uncover specialized properties of bone marrow in adult and ageing skull. Specifically, we show that the skull bone marrow undergoes lifelong expansion involving vascular growth, which results in an increasing contribution to total haematopoietic output. Furthermore, skull is largely protected against major hallmarks of ageing, including upregulation of pro-inflammatory cytokines, adipogenesis and loss of vascular integrity. Conspicuous rapid and dynamic changes to the skull vasculature and bone marrow are induced by physiological alterations, namely pregnancy, but also pathological challenges, such as stroke and experimental chronic myeloid leukaemia. These responses are highly distinct from femur, the most extensively studied bone marrow compartment. We propose that skull harbours a protected and dynamically expanding bone marrow microenvironment, which is relevant for experimental studies and, potentially, for clinical treatments in humans.
Suggested Citation
Bong Ihn Koh & Vishal Mohanakrishnan & Hyun-Woo Jeong & Hongryeol Park & Kai Kruse & Young Jun Choi & Melina Nieminen-Kelhä & Rahul Kumar & Raquel S. Pereira & Susanne Adams & Hyuek Jong Lee & M. Gabr, 2024.
"Adult skull bone marrow is an expanding and resilient haematopoietic reservoir,"
Nature, Nature, vol. 636(8041), pages 172-181, December.
Handle:
RePEc:nat:nature:v:636:y:2024:i:8041:d:10.1038_s41586-024-08163-9
DOI: 10.1038/s41586-024-08163-9
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