Hematopoietic Stem Cell Dynamics Are Regulated by Progenitor Demand: Lessons from a Quantitative Modeling Approach. (3rd April 2019)

• Record Type: Journal Article
• Authors: Klose, Markus; Florian, Maria Carolina; Gerbaulet, Alexander; Geiger, Hartmut; Glauche, Ingmar
• Is Part Of: Stem cells. Volume 37:Number 7(2019)
• Page Start: 948
• Page End: 957
• Publication Date: 2019-04-03
• Subjects: Hematopoiesis -- Hematopoietic stem cells -- Regeneration -- Aging -- Mathematical modeling; Cloning -- Periodicals; Clone cells -- Periodicals; Stem cells -- Periodicals; Cell Differentiation -- Periodicals; Cell Division -- Periodicals; Clone Cells -- Periodicals; Hematopoietic Stem Cells -- Periodicals; Stem Cells -- Periodicals; 571.84
• DOI: 10.1002/stem.3005
• Languages: English
• ISSNs: 1066-5099

Abstract

Abstract: The prevailing view on murine hematopoiesis and on hematopoietic stem cells (HSCs) in particular derives from experiments that are related to regeneration after irradiation and HSC transplantation. However, over the past years, different experimental techniques have been developed to investigate hematopoiesis under homeostatic conditions, thereby providing access to proliferation and differentiation rates of hematopoietic stem and progenitor cells in the unperturbed situation. Moreover, it has become clear that hematopoiesis undergoes distinct changes during aging with large effects on HSC abundance, lineage contribution, asymmetry of division, and self-renewal potential. However, it is currently not fully resolved how stem and progenitor cells interact to respond to varying demands and how this balance is altered by an aging-induced shift in HSC polarity. Aiming toward a conceptual understanding, we introduce a novel in silico model to investigate the dynamics of HSC response to varying demand. By introducing an internal feedback within a heterogeneous HSC population, the model is suited to consistently describe both hematopoietic homeostasis and regeneration, including the limited regulation of HSCs in the homeostatic situation. The model further explains the age-dependent increase in phenotypic HSCs as a consequence of the cells' inability to preserve divisional asymmetry. Our model suggests a dynamically regulated population of intrinsically asymmetrically dividing HSCs as suitable control mechanism that adheres with many qualitative and quantitative findings on hematopoietic recovery after stress and aging. The modeling approach thereby illustrates how a mathematical formalism can support both the conceptual and the quantitative understanding of regulatory principles in HSC biology. : Abstract : We present a simple mathematical model for the regulation of populations of murine hematopoietic stem cells (consisting of repopulating hematopoietic stem cells and maintaining hematopoietic stem cells) and progenitors. By assuming that repopulating hematopoietic stem cell proliferation is driven by downstream demand and by incorporating the ability of repopulating hematopoietic stem cells to divide asymmetrically, we are able to explain the observed aging-related increase in repopulating hematopoietic stem cell numbers due to a decline in their capability to divide asymmetrically as well as recent experimental findings on specific depletion of hematopoietic stem and progenitor cells and their recovery. We further investigate the system reaction, if similar experiments are conducted in old mice.