4.5 Article

Perivascular Secretome Influences Hematopoietic Stem Cell Maintenance in a Gelatin Hydrogel

Journal

ANNALS OF BIOMEDICAL ENGINEERING
Volume 49, Issue 2, Pages 780-792

Publisher

SPRINGER
DOI: 10.1007/s10439-020-02602-0

Keywords

Tissue engineering; Biomaterial niche; Hematopoietic stem cell

Funding

  1. National Institute of Diabetes and Digestive and Kidney Diseases of the National Institutes of Health [R01 DK099528]
  2. National Institute of Biomedical Imaging and Bioengineering of the National Institutes of Health [R21 EB018481]
  3. Department of Chemical & Biomolecular Engineering
  4. Institute for Genomic Biology at the University of Illinois at Urbana-Champaign

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The study developed and characterized a three-dimensional perivascular tissue model to investigate the influence of the perivascular secretome on HSC behavior, finding that perivascular conditioned media promoted maintenance of a greater fraction of hematopoietic stem and progenitor cells within a 4-day culture period.
Adult hematopoietic stem cells (HSCs) produce the body's full complement of blood and immune cells. They reside in specialized microenvironments, or niches, within the bone marrow. The perivascular niche near blood vessels is believed to help maintain primitive HSCs in an undifferentiated state but demonstration of this effect is difficult.In vivostudies make it challenging to determine the direct effect of the endosteal and perivascular niches as they can be in close proximity, and two-dimensionalin vitrocultures often lack an instructive extracellular matrix environment. We describe a tissue engineering approach to develop and characterize a three-dimensional perivascular tissue model to investigate the influence of the perivascular secretome on HSC behavior. We generate 3D endothelial networks in methacrylamide-functionalized gelatin hydrogels using human umbilical vein endothelial cells (HUVECs) and mesenchymal stromal cells (MSCs). We identify a subset of secreted factors important for HSC function, and examine the response of primary murine HSCs in hydrogels to the perivascular secretome. Within 4 days of culture, perivascular conditioned media promoted maintenance of a greater fraction of hematopoietic stem and progenitor cells. This work represents an important first-generation perivascular model to investigate the role of niche secreted factors on the maintenance of primary HSCs.

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