The role of the haematopoietic stem cell niche in development and ageing

• Published in: Nature reviews. Molecular cell biology Vol. 26; no. 1; pp. 32 - 50
• Main Authors: Cain, Terri L., Derecka, Marta, McKinney-Freeman, Shannon
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 01.01.2025; Nature Publishing Group
• Subjects: 631/136/2139; 631/136/232; 631/532/1542; Aging; Aging - physiology; Animals; Aorta; Biochemistry; Biomedical and Life Sciences; Blood; Bone marrow; Bone Marrow - embryology; Bone Marrow - metabolism; Cancer Research; Cell Biology; Cell culture; Cell Differentiation - physiology; Developmental Biology; Endothelium; Fetuses; Hematopoiesis - physiology; Hematopoietic stem cells; Hematopoietic Stem Cells - cytology; Hematopoietic Stem Cells - metabolism; Hemopoiesis; Hepatocytes; Humans; Life Sciences; Liver diseases; Microenvironments; Microscopy; Ontogeny; Osteoprogenitor cells; Progenitor cells; Review Article; Specifications; Stem Cell Niche - physiology; Stem Cells; Tracing; Transcriptomics
• ISSN: 1471-0072; 1471-0080; 1471-0080
• DOI: 10.1038/s41580-024-00770-8

Blood production depends on rare haematopoietic stem cells (HSCs) and haematopoietic stem and progenitor cells (HSPCs) that ultimately take up residence in the bone marrow during development. HSPCs and HSCs are subject to extrinsic regulation by the bone marrow microenvironment, or niche. Studying the interactions between HSCs and their niche is critical for improving ex vivo culturing conditions and genetic manipulation of HSCs, which is pivotal for improving autologous HSC therapies and transplantations. Additionally, understanding how the complex molecular network in the bone marrow is altered during ageing is paramount for developing novel therapeutics for ageing-related haematopoietic disorders. HSCs are unique amongst stem and progenitor cell pools in that they engage with multiple physically distinct niches during their ontogeny. HSCs are specified from haemogenic endothelium in the aorta, migrate to the fetal liver and, ultimately, colonize their final niche in the bone marrow. Recent studies employing single-cell transcriptomics and microscopy have identified novel cellular interactions that govern HSC specification and engagement with their niches throughout ontogeny. New lineage-tracing models and microscopy tools have raised questions about the numbers of HSCs specified, as well as the functional consequences of HSCs interacting with each developmental niche. Advances have also been made in understanding how these niches are modified and perturbed during ageing, and the role of these altered interactions in haematopoietic diseases. In this Review, we discuss these new findings and highlight the questions that remain to be explored. Blood production depends on haematopoietic stem cells (HSCs) and progenitor cells, which are regulated by their microenvironment or niche. New lineage-tracing models and microscopy tools are increasing the understanding of HSC specification and function, and how stem cell–niche interactions are perturbed during ageing.