Author
Listed:
- Qingqing Wu
(Cincinnati Children’s Hospital Medical Center
University of Science and Technology of China)
- Jizhou Zhang
(Cincinnati Children’s Hospital Medical Center
University of Science and Technology of China)
- Sumit Kumar
(Cincinnati Children’s Hospital Medical Center)
- Siyu Shen
(Cincinnati Children’s Hospital Medical Center)
- Morgan Kincaid
(Cincinnati Children’s Hospital Medical Center)
- Courtney B. Johnson
(Cincinnati Children’s Hospital Medical Center)
- Yanan Sophia Zhang
(Cincinnati Children’s Hospital Medical Center)
- Raphaël Turcotte
(Massachusetts General Hospital and Harvard Medical School
Albert Einstein College of Medicine)
- Clemens Alt
(Massachusetts General Hospital and Harvard Medical School)
- Kyoko Ito
(Albert Einstein College of Medicine)
- Shelli Homan
(Cincinnati Children’s Hospital Medical Center)
- Bryan E. Sherman
(University of Cincinnati College of Medicine)
- Tzu-Yu Shao
(University of Cincinnati College of Medicine
University of Cincinnati College of Medicine)
- Anastasiya Slaughter
(Cincinnati Children’s Hospital Medical Center
University of Cincinnati College of Medicine)
- Benjamin Weinhaus
(Cincinnati Children’s Hospital Medical Center
University of Cincinnati College of Medicine)
- Baobao Song
(University of Cincinnati College of Medicine
Cincinnati Children’s Hospital Medical Center)
- Marie Dominique Filippi
(Cincinnati Children’s Hospital Medical Center
University of Cincinnati College of Medicine)
- H. Leighton Grimes
(Cincinnati Children’s Hospital Medical Center
Cincinnati Children’s Hospital Medical Center
University of Cincinnati College of Medicine)
- Charles P. Lin
(Harvard Medical School
Harvard Stem Cell Institute)
- Keisuke Ito
(Albert Einstein College of Medicine
Albert Einstein College of Medicine)
- Sing Sing Way
(University of Cincinnati College of Medicine
University of Cincinnati College of Medicine)
- J. Matthew Kofron
(University of Cincinnati College of Medicine
Cincinnati Children’s Hospital Medical Center)
- Daniel Lucas
(Cincinnati Children’s Hospital Medical Center
University of Cincinnati College of Medicine)
Abstract
The bone marrow adjusts blood cell production to meet physiological demands in response to insults. The spatial organization of normal and stress responses are unknown owing to the lack of methods to visualize most steps of blood production. Here we develop strategies to image multipotent haematopoiesis, erythropoiesis and lymphopoiesis in mice. We combine these with imaging of myelopoiesis1 to define the anatomy of normal and stress haematopoiesis. In the steady state, across the skeleton, single stem cells and multipotent progenitors distribute through the marrow enriched near megakaryocytes. Lineage-committed progenitors are recruited to blood vessels, where they contribute to lineage-specific microanatomical structures composed of progenitors and immature cells, which function as the production sites for each major blood lineage. This overall anatomy is resilient to insults, as it was maintained after haemorrhage, systemic bacterial infection and granulocyte colony-stimulating factor (G-CSF) treatment, and during ageing. Production sites enable haematopoietic plasticity as they differentially and selectively modulate their numbers and output in response to insults. We found that stress responses are variable across the skeleton: the tibia and the sternum respond in opposite ways to G-CSF, and the skull does not increase erythropoiesis after haemorrhage. Our studies enable in situ analyses of haematopoiesis, define the anatomy of normal and stress responses, identify discrete microanatomical production sites that confer plasticity to haematopoiesis, and uncover unprecedented heterogeneity of stress responses across the skeleton.
Suggested Citation
Qingqing Wu & Jizhou Zhang & Sumit Kumar & Siyu Shen & Morgan Kincaid & Courtney B. Johnson & Yanan Sophia Zhang & Raphaël Turcotte & Clemens Alt & Kyoko Ito & Shelli Homan & Bryan E. Sherman & Tzu-Yu, 2024.
"Resilient anatomy and local plasticity of naive and stress haematopoiesis,"
Nature, Nature, vol. 627(8005), pages 839-846, March.
Handle:
RePEc:nat:nature:v:627:y:2024:i:8005:d:10.1038_s41586-024-07186-6
DOI: 10.1038/s41586-024-07186-6
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