Abstract

The bone marrow (BM) microenvironment, also called the BM niche, is essential for the maintenance of fully functional blood cell formation (hematopoiesis) throughout life. Under physiologic conditions the niche protects hematopoietic stem cells (HSCs) from sustained or overstimulation. Acute or chronic stress deregulates hematopoiesis and some of these alterations occur indirectly via the niche. Effects on niche cells include skewing of its cellular composition, specific localization and molecular signals that differentially regulate the function of HSCs and their progeny. Importantly, while acute insults display only transient effects, repeated or chronic insults lead to sustained alterations of the niche, resulting in HSC deregulation. We here describe how changes in BM niche composition (ecosystem) and structure (remodeling) modulate activation of HSCs in situ. Current knowledge has revealed that upon chronic stimulation, BM remodeling is more extensive and otherwise quiescent HSCs may be lost due to diminished cellular maintenance processes, such as autophagy, ER stress response, and DNA repair. Features of aging in the BM ecology may be the consequence of intermittent stress responses, ultimately resulting in the degeneration of the supportive stem cell microenvironment. Both chronic stress and aging impair the functionality of HSCs and increase the overall susceptibility to development of diseases, including malignant transformation. To understand functional degeneration, an important prerequisite is to define distinguishing features of unperturbed niche homeostasis in different settings. A unique setting in this respect is xenotransplantation, in which human cells depend on niche factors produced by other species, some of which we will review. These insights should help to assess deviations from the steady state to actively protect and improve recovery of the niche ecosystem in situ to optimally sustain healthy hematopoiesis in experimental and clinical settings.

Highlights

  • SCOPE OF THIS REVIEWThe bone marrow (BM) niche is an important gate-keeper in the maintenance of the blood cell system, which is unique in its circulation throughout the body

  • The above data may help to resolve the puzzling observation that induced niche remodeling in which specific niche cell populations are deleted by using iDTR/diphtheria toxin targeting, such as mesenchymal Nes+, Lepr+ or Cspg4+ (NG2+) cells (Méndez-Ferrer et al, 2008; Kunisaki et al, 2013; Acar et al, 2015), Cxcl4+ megakaryocytes (Bruns et al, 2014; Zhao et al, 2014), or Gfap+ Schwann cells (Yamazaki et al, 2011), all lead to a declining support of hematopoiesis and, over time, to hematopoietic stem cell (HSC) attrition and BM failure

  • It is an exciting time for research about the interrelationship of HSCs and their BM niche

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Summary

The Hematopoietic Bone Marrow Niche Ecosystem

Features of aging in the BM ecology may be the consequence of intermittent stress responses, resulting in the degeneration of the supportive stem cell microenvironment. Both chronic stress and aging impair the functionality of HSCs and increase the overall susceptibility to development of diseases, including malignant transformation. A unique setting in this respect is xenotransplantation, in which human cells depend on niche factors produced by other species, some of which we will review These insights should help to assess deviations from the steady state to actively protect and improve recovery of the niche ecosystem in situ to optimally sustain healthy hematopoiesis in experimental and clinical settings

SCOPE OF THIS REVIEW
THE RESPONSE OF THE BM NICHE TO ACUTE STRESS
CHANGES IN THE BM NICHE AND THE DEVELOPMENT OF CHRONIC MALIGNANCIES
THE FACTORS SUPPORTING HUMAN HSCs IN THE MURINE BM NICHE
No expression No expression
Findings
CONCLUDING REMARKS
Full Text
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