Human fetal liver stromal cells expressing erythropoietin promote hematopoietic development from human embryonic stem cells

Cell Reprogram. 2012 Feb;14(1):88-97. doi: 10.1089/cell.2011.0013.

Abstract

Blood cells transfusion and hematopoietic stem cells (HSCs) transplantation are important methods for cell therapy. They are widely used in the treatment of incurable hematological disorder, infectious diseases, genetic diseases, and immunologic deficiency. However, their availability is limited by quantity, capacity of proliferation and the risk of blood transfusion complications. Recently, human embryonic stem cells (hESCs) have been shown to be an alternative resource for the generation of hematopoietic cells. In the current study, we describe a novel method for the efficient production of hematopoietic cells from hESCs. The stable human fetal liver stromal cell lines (hFLSCs) expressing erythropoietin (EPO) were established using the lentiviral system. We observed that the supernatant from the EPO transfected hFLSCs could induce the hESCs differentiation into hematopoietic cells, especially erythroid cells. They not only expressed fetal and embryonic globins but also expressed the adult-globin chain on further maturation. In addition, these hESCs-derived erythroid cells possess oxygen-transporting capacity, which indicated hESCs could generate terminally mature progenies. This should be useful for ultimately developing an animal-free culture system to generate large numbers of erythroid cells from hESCs and provide an experimental model to study early human erythropoiesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Differentiation / drug effects
  • Cell Differentiation / physiology
  • Cell Line
  • Cells, Cultured
  • Culture Media, Conditioned / pharmacology
  • Embryonic Stem Cells / cytology*
  • Embryonic Stem Cells / physiology
  • Erythroid Cells / cytology
  • Erythroid Cells / metabolism
  • Erythropoietin / genetics
  • Erythropoietin / metabolism*
  • Fetal Globulins / metabolism
  • Fetus / cytology*
  • Hematopoiesis / physiology*
  • Humans
  • Lentivirus / genetics
  • Liver / cytology*
  • Liver / embryology
  • Liver / metabolism
  • Stromal Cells / cytology*
  • Stromal Cells / metabolism*
  • Transfection

Substances

  • Culture Media, Conditioned
  • Fetal Globulins
  • Erythropoietin