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RESEARCH PAPER / 2025-10-02

Regulation of Hematopoietic Stem Cell Dormancy and Quiescence: Insights into Regeneration and Disease.

Jasmin Rettkowski, Nina Cabezas-Wallscheid

Laboratory of Stem Cell Biology and Ageing, Department of Health Sciences and Technology, Swiss Federal Institute of Technology (ETH Zürich), Zürich, Switzerland; email: [email protected], [email protected]. · pubmed

Abstract

Stem cells are undifferentiated cells capable of self-renewal and differentiation into specialized cell types, forming the foundation of tissue maintenance and repair. In the blood system, this process is known as hematopoiesis. Hematopoietic stem cells (HSCs), positioned at the apex of the hematopoietic hierarchy, have the unique ability to reconstitute the hematopoietic system long-term. HSC stemness is defined by multipotency, allowing differentiation into all blood lineages, and self-renewal, maintaining the stem cell pool. A fundamental property of HSCs is quiescence, which refers to a reversible inactive cell cycle state that preserves their self-renewal potential. Dormant HSCs represent a subset of quiescent stem cells with minimal division rates and the most potent stemness. Dysregulation of dormancy and quiescence is linked to HSC dysfunction. Here, we explore mechanisms regulating HSC dormancy and quiescence under homeostatic and stress conditions. Finally, we describe how factors such as aging, inflammation, and malignancies disrupt these states.

The following analysis is generated by AI and may contain errors. It is separate from the authors’ abstract and is not peer review.

Research summary

The paper explores the mechanisms regulating hematopoietic stem cell dormancy and quiescence, linking these processes to aging and dysfunction. Understanding and potentially manipulating HSC dormancy and quiescence could provide insights into the root causes of aging and age-related diseases, making it relevant to longevity research.

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