Human serum albumin promotes self-renewal and expansion of umbilical cord blood CD34 hematopoietic stem/progenitor cells.

BACKGROUND

We investigated the effect of human serum albumin (HSA) on human umbilical cord blood (UCB) CD34 hematopoietic stem/progenitor cells (HSPCs) cultured and transplanted .

METHODS

Human umbilical cord blood mononuclear cells were obtained by density gradient centrifugation. CD34 cells were then sorted by CD34 conjugated magnetic microbeads. The sorted cells were cultured with or without HSA for 8 days . After 8 days, all cells were harvested for flow phenotyping and colony formation cell (CFC) experiments. The cells were injected into immunodeficient mice (NOD/Shi-scid/IL2Rγnull, NOG) via intravenous injections. From 4 weeks post-transplantation, flow cytometry was used to calculate human cell chimerism in the peripheral blood (PB) every 2 weeks. Flow phenotyping of human cell chimerism in bone marrow and spleen was calculated 16 weeks post-transplantation.

RESULTS

Compared to the control group, CD34 cells cultured with HSA increased significantly . The long-term engraftment of HSPCs and the hematopoietic multilineage reconstruction capacity were preserved by HSA. Normal engraftment of human cells could be maintained via HSA treatment could maintain normal engraftment of human cells in recipient PB.

CONCLUSIONS

Here, we found that HSA was beneficial to maintaining CD34 cell expansion and short-term colony formation and optimizing multilineage reconstitution in immunodeficient mice .