Zbtb46-dependent altered developmental program in embryonic stem cell-derived blood cell progenitors.
Pal BotoTimea Beatrix GerzsenyiAdel LengyelBalint SzunyogIstvan SzatmariPublished in: Stem cells (Dayton, Ohio) (2021)
Zbtb46 is a recently identified dendritic cell (DC)-specific transcription factor with poorly defined biology. Although Zbtb46 is highly expressed in conventional DCs, evidence also points to its presence in erythroid progenitors and endothelial cells suggesting that this factor might influence the early hematopoietic development. Here, we probe the effect of this transcription factor in embryonic stem cell (ESC)-derived blood cell progenitors using chemically inducible mouse cell lines. Unexpectedly, forced expression of this protein elicited a broad repressive effect at the early stage of ESC differentiation. Ectopic expression of Zbtb46 interfered with the mesoderm formation and cell proliferation was also negatively impacted. More importantly, reduced number of CD11b+ myeloid blood cells were generated from ESC-derived Flk1+ mesoderm cells in the presence of Zbtb46. Consistent with this finding, our gene expression profiling revealed that numerous myeloid and immune response related genes, including Irf8, exhibited lower expression in the Zbtb46-primed cells. Despite these repressive effects, however, Zbtb46 overexpression was associated with enhanced formation of erythroid blood cell colonies and increased adult hemoglobin (Hbb-b1) expression at the early phase of ESC differentiation. Moreover, elevated percent of CD105 (Endoglin) positive cells were detected in the Zbtb46-primed samples. In summary, our results support that Zbtb46 suppresses the ESC-derived myeloid development and diverts mesoderm cells toward erythroid developmental pathway. Moreover, our transcriptomic data provide a resource for exploration of the Zbtb46 regulatory network in ESC-derived progenitors.
Keyphrases
- induced apoptosis
- dendritic cells
- transcription factor
- cell cycle arrest
- poor prognosis
- cell proliferation
- early stage
- stem cells
- single cell
- immune response
- signaling pathway
- cell therapy
- binding protein
- gene expression
- oxidative stress
- acute myeloid leukemia
- regulatory t cells
- machine learning
- squamous cell carcinoma
- genome wide
- pi k akt
- radiation therapy
- small molecule
- genome wide identification
- mesenchymal stem cells
- toll like receptor
- long non coding rna
- pluripotent stem cells
- fluorescent probe
- protein protein