2007
DOI: 10.1111/j.1440-169x.2007.00925.x
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Distinct hemogenic potential of endothelial cells and CD41+ cells in mouse embryos

Abstract: Definitive hematopoietic progenitor cells have been thought to develop from the vascular endothelium located in the aorta-gonad-mesonephros region of the mouse embryo. However, several recent findings have suggested that most hematopoietic progenitors are derived from non-endothelial precursor cells expressing CD41. We characterized two distinct precursor populations of definitive hematopoietic cell lineages, vascular endothelial (VE)-cadherin + CD41 -CD45 -endothelial cells and CD41 + CD45 -non-endothelial pr… Show more

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Cited by 31 publications
(28 citation statements)
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“…Flow cytometry analysis was performed to evaluate the B lineage cells in the bone marrow, mononuclear cells in the circulating blood, and splenocytes as described (Hashimoto et al, 2007;Kim-Saijo et al, 2008) using a FACSCalibur HG (BD Biosciences). The data were analyzed with BD CellQuest Pro (BD Biosciences).…”
Section: Methodsmentioning
confidence: 99%
“…Flow cytometry analysis was performed to evaluate the B lineage cells in the bone marrow, mononuclear cells in the circulating blood, and splenocytes as described (Hashimoto et al, 2007;Kim-Saijo et al, 2008) using a FACSCalibur HG (BD Biosciences). The data were analyzed with BD CellQuest Pro (BD Biosciences).…”
Section: Methodsmentioning
confidence: 99%
“…Since CD41 marks megakaryocytes and all hematopoietic progenitors in the early embryo (Bertrand et al, 2005;Corbel and Salaun, 2002;Ferkowicz et al, 2003;Mikkola et al, 2003), these cells cannot be considered to be endothelial either. Although some CD41 cells express VE-cadherin, they lack endothelial potential (Hashimoto et al, 2007;Li et al, 2005). The role of VE-cadherin in pre-dHSCs might be in facilitating interactions with endothelial cells and mediating essential signaling (Carmeliet et al, 1999).…”
Section: Identification Of Pre-dhscsmentioning
confidence: 99%
“…The YS cells were filtered through a 30-lm mesh (Cell Trics; Perteck, Mü nster, Germany), and stained with phycoerythrin (PE)-conjugated anti-mouse CD45 (30-F11; eBioscience, San Diego, CA, USA) and allophycocyanin (APC)-conjugated anti-mouse c-Kit (2B8; eBioscience) antibodies. The YS cells were also stained with fluorescein isothiocyanate-conjugated anti-mouse CD34 (RAM34; eBioscience), anti-mouse Mac-1 (M1 ⁄ 70; eBioscience), anti-mouse vascular endothelial-cadherin (VECD1) (Matsuyoshi et al 1997;Hashimoto et al 2007) …”
Section: Fractionation Of Ys Cells By Flow Cytometrymentioning
confidence: 99%