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Zbtb46‐dependent altered developmental program in embryonic stem cell‐derived blood cell progenitors
Author(s) -
Boto Pal,
Gerzsenyi Timea Beatrix,
Lengyel Adel,
Szunyog Balint,
Szatmari Istvan
Publication year - 2021
Publication title -
stem cells
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.159
H-Index - 229
eISSN - 1549-4918
pISSN - 1066-5099
DOI - 10.1002/stem.3424
Subject(s) - biology , microbiology and biotechnology , progenitor cell , embryonic stem cell , mesoderm , stem cell , haematopoiesis , cellular differentiation , immunology , myeloid , lineage markers , ectopic expression , gata2 , cell culture , genetics , gene
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.

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