作者: Lina Dahl , Karin Richter , Anna-Carin Hägglund , Leif Carlsson
DOI: 10.1371/JOURNAL.PONE.0002025
关键词: Embryoid body 、 Cellular differentiation 、 Stem cell factor 、 Cell biology 、 Adult stem cell 、 Embryonic stem cell 、 Stem cell 、 Biology 、 Endothelial stem cell 、 Progenitor cell
摘要: The molecular mechanisms regulating the expansion of hematopoietic system including stem cells (HSCs) in fetal liver during embryonic development are largely unknown. LIM-homeobox gene Lhx2 is a candidate regulator hematopoiesis since it expressed and Lhx2−/− mice die utero due to severe anemia. Moreover, expression (ES) cell-derived embryoid bodies (EBs) can lead generation HSC-like cell lines. To further define role this transcription factor regulation, we generated ES lines that enabled tet-inducible Lhx2. Using approach observed synergises with specific signalling pathways, resulting increased frequency colony forming developing EB cells. increase growth factor-responsive progenitor directly correlates efficiency generating lines, suggesting induce self-renewal distinct multipotential EBs. Signalling via c-kit tyrosine kinase receptor gp130 signal transducer by IL-6 necessary sufficient for induced self-renewal. While inducing cells, inhibited proliferation primitive erythroid precursor interfered early commitment, indicating striking lineage specificity effect.