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Human definitive hematopoietic specification from pluripotent stem cells is regulated by mesodermal expression of CDX4.
Creamer, J Philip; Dege, Carissa; Ren, Qihao; Ho, Jolie T K; Valentine, Mark C; Druley, Todd E; Sturgeon, Christopher M.
Afiliación
  • Creamer JP; Division of Hematology, Department of Medicine.
  • Dege C; Division of Hematology, Department of Medicine.
  • Ren Q; Division of Hematology, Department of Medicine.
  • Ho JTK; Division of Hematology, Department of Medicine.
  • Valentine MC; Department of Pediatrics, and.
  • Druley TE; Department of Pediatrics, and.
  • Sturgeon CM; Division of Hematology, Department of Medicine.
Blood ; 129(22): 2988-2992, 2017 06 01.
Article en En | MEDLINE | ID: mdl-28408465
ABSTRACT
The generation of hematopoietic stem cells from human pluripotent stem cells (hPSCs) is a major goal for regenerative medicine. Achieving this goal is complicated by our incomplete understanding of the mechanism regulating definitive hematopoietic specification. We used our stage-specific hPSC differentiation method to obtain and identify, via CD235a expression, mesoderm harboring exclusively primitive or definitive hematopoietic potential to understand the genetic regulation of definitive hematopoietic specification. Whole-transcriptome gene expression analyses on WNT-dependent KDR+CD235a- definitive hematopoietic mesoderm and WNT-independent KDR+CD235a+ primitive hematopoietic mesoderm revealed strong CDX gene expression within definitive hematopoietic mesoderm. Temporal expression analyses revealed that CDX4 was expressed exclusively within definitive hematopoietic KDR+CD235a- mesoderm in a WNT- and fibroblast growth factor-dependent manner. We found that exogenous CDX4 expression exclusively during mesoderm specification resulted in a >90% repression in primitive hematopoietic potential, but conferred fivefold greater definitive hematopoietic potential, similar to that observed following WNT stimulation. In contrast, CDX4 knockout hPSCs had intact primitive hematopoietic potential, but exhibited a fivefold decrease in multilineage definitive hematopoietic potential. Taken together, these findings indicate that CDX4 is a critical transcription factor in the regulation of human definitive hematopoietic specification, and provides a mechanistic basis for WNT-mediated definitive hematopoietic specification from hPSCs.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Células Madre Hematopoyéticas / Proteínas de Homeodominio / Células Madre Pluripotentes / Hematopoyesis Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Blood Año: 2017 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Células Madre Hematopoyéticas / Proteínas de Homeodominio / Células Madre Pluripotentes / Hematopoyesis Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Blood Año: 2017 Tipo del documento: Article