TOWARDS MIMICKING THE FETAL LIVER NICHE: THE INFLUENCE OF ELASTICITY AND OXYGEN TENSION ON HEMATOPOIETIC STEM/PROGENITOR CELLS CULTURED IN 3D FIBRIN HYDROGELS
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Date
2020-09-02
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Abstract
Hematopoietic stem/progenitor cells (HSPCs) are responsible for the generation of blood
cells throughout life. It is believed that, in addition to soluble cytokines and niche cells, biophysical cues
like elasticity and oxygen tension are responsible for the orchestration of stem cell fate. Although
several studies have examined the effects of bone marrow (BM) niche elasticity on HSPC behavior,
no study has yet investigated the effects of the elasticity of other niche sites like the fetal liver (FL),
where HSPCs expand more extensively. In this study, we evaluated the effect of matrix stiffness
values similar to those of the FL on BM-derived HSPC expansion. We first characterized the elastic
modulus of murine FL tissue at embryonic day E14.5. Fibrin hydrogels with similar stiffness
values as the FL (soft hydrogels) were compared with stiffer fibrin hydrogels (hard hydrogels) and
with suspension culture. We evaluated the expansion of total nucleated cells (TNCs), Lin−/cKit+
cells, HSPCs (Lin−/Sca+/cKit+ (LSK) cells), and hematopoietic stem cells (HSCs: LSK- Signaling
Lymphocyte Activated Molecule (LSK-SLAM) cells) when cultured in 5% O2 (hypoxia) or in normoxia.
After 10 days, there was a significant expansion of TNCs and LSK cells in all culture conditions at both
levels of oxygen tension. LSK cells expanded more in suspension culture than in both fibrin hydrogels,
whereas TNCs expanded more in suspension culture and in soft hydrogels than in hard hydrogels,
particularly in normoxia. The number of LSK-SLAM cells was maintained in suspension culture and
in the soft hydrogels but not in the hard hydrogels. Our results indicate that both suspension culture
and fibrin hydrogels allow for the expansion of HSPCs and more differentiated progeny whereas stiff
environments may compromise LSK-SLAM cell expansion. This suggests that further research using
softer hydrogels with stiffness values closer to the FL niche is warranted.
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Keywords
fibrin hydrogel, elastic modulus, hematopoietic stem cells, fetal liver niche, 3D cell encapsulation, oxygen tension