首页> 外文期刊>Biochemical and Biophysical Research Communications >Activin A in combination with OP9 cells facilitates development of Flk-1(+) PDGFR alpha(-) and Flk-1(+) PDGFR alpha(+) hematopoietic mesodermal cells from murine embryonic stem cells
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Activin A in combination with OP9 cells facilitates development of Flk-1(+) PDGFR alpha(-) and Flk-1(+) PDGFR alpha(+) hematopoietic mesodermal cells from murine embryonic stem cells

机译:激活素A与OP9细胞结合可促进来自小鼠胚胎干细胞的Flk-1(+)PDGFR alpha(-)和Flk-1(+)PDGFR alpha(+)造血中胚层细胞的发育

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摘要

Lateral mesoderm-derived hemogenic endothelial cells are known to originate the definitive hematopoietic lineage in mouse embryogenesis. The developmental process of the definitive hematopoietic lineage can be recapitulated by inducing differentiation of mouse embryonic stem (ES) cells in a co-culture system with OP9 stromal cells. However, the signaling molecules that can modulate the development of the definitive hematopoietic lineage in the OP9 co-culture system have yet to be identified. Here we report that activin A enhanced the hematopoietic potential of endothelial cells derived from ES cells in the OP9 co-culture system. Activin A in combination with OP9 cells augmented development of Flk-1(+) PDGFR alpha(+) early mesodermal cells and Flk-1(+) PDGFR alpha(-) lateral mesodermal cells from ES cells. These Flk-1(+) mesodermal cells further differentiated into CD41(+) endothelial cells, which preferentially possessed high hematopoietic potential. Furthermore, Flk-1(+) PDGFR alpha(+) cells but not Flk-1(+) PDGFR alpha(-) cells produced hematopoietic progenitors with a bimodal pattern when cultured as an aggregate with OP9 cells. Our results suggest that activin A in combination with OP9 cells facilitates differentiation of ES cells to Flk-1(+) mesodermal cells, which encompass various precursors that separately contribute to the development of hematopoietic lineages. (C) 2015 Elsevier Inc. All rights reserved.
机译:已知中胚层外源性造血内皮细胞在小鼠胚胎发生中起源于确定的造血谱系。可以通过在与OP9基质细胞共培养的系统中诱导小鼠胚胎干(ES)细胞分化来概括确定性造血谱系的发育过程。然而,尚未确定可调节OP9共培养系统中确定的造血谱系发育的信号分子。在这里我们报道激活素A增强了OP9共培养系统中源自ES细胞的内皮细胞的造血潜能。激活素A与OP9细胞结合增强了ES细胞Flk-1(+)PDGFR alpha(+)早期中胚层细胞和Flk-1(+)PDGFR alpha(-)外侧中胚层细胞的发育。这些Flk-1(+)中胚层细胞进一步分化为CD41(+)内皮细胞,后者具有较高的造血潜能。此外,Flk-1(+)PDGFR alpha(+)细胞而不是Flk-1(+)PDGFR alpha(-)细胞与OP9细胞一起培养时,会产生具有双峰模式的造血祖细胞。我们的研究结果表明,激活素A与OP9细胞结合可促进ES细胞分化为Flk-1(+)中胚层细胞,其中包括各种前体,它们分别有助于造血谱系的发育。 (C)2015 Elsevier Inc.保留所有权利。

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