2013
DOI: 10.1016/j.exphem.2013.06.005
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Understanding the role of the microenvironment during definitive hemopoietic development

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Cited by 25 publications
(24 citation statements)
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“…Migration is essential for fetal hematopoiesis as multiple sites allow different inductive signals from the microenvironments to support hematopoietic development. 66 We show that, in WT mice, FL SDF-1α concentration progressively decreased from E14.5, with HSC migrating from the FL to the BM after E16.5. The accumulated data in other in vivo and in vitro contexts, including the homing of HSC and progenitors to BM, 20 suggest this occurs due to a co-ordinated sequence of events including: 1) a polarized source of SDF-1 developing; 2) the cells producing projections extending towards the SDF-1, with cell-associated CD44 migrating into the projections; and 3) CD44 binding to an external source of hyaluronan and the cells undergoing trans-endothelial migration.…”
Section: Cd44mentioning
confidence: 63%
“…Migration is essential for fetal hematopoiesis as multiple sites allow different inductive signals from the microenvironments to support hematopoietic development. 66 We show that, in WT mice, FL SDF-1α concentration progressively decreased from E14.5, with HSC migrating from the FL to the BM after E16.5. The accumulated data in other in vivo and in vitro contexts, including the homing of HSC and progenitors to BM, 20 suggest this occurs due to a co-ordinated sequence of events including: 1) a polarized source of SDF-1 developing; 2) the cells producing projections extending towards the SDF-1, with cell-associated CD44 migrating into the projections; and 3) CD44 binding to an external source of hyaluronan and the cells undergoing trans-endothelial migration.…”
Section: Cd44mentioning
confidence: 63%
“…The interplay between these components predominantly keeps HSCs in a quiescent state, but can also accelerate mature blood cell replenishment in cases of urgent need, such as during infection or excessive blood loss. A great number of molecules described in the adult BM niche display functions as HSC regulators, overlapping in function or interacting with each other to modulate HSC behavior [36]. The discovery that perturbations of the HSC niche can lead to hematopoietic disorders, has outlined the crucial role of this niche in the control of HSC activity and thus on immune cell formation [37].…”
Section: Metabolic Disorders and Bone Marrow Hematopoiesismentioning
confidence: 99%
“…This information is particularly useful for identifying methods of generating HSCs from pluripotent stem cells. A recent review by Cao et al [1] examines the hematopoietic microenvironment throughout development with extensive coverage of the fetal liver (FL) and beyond. Here, we provide a complementary review concentrating on the earlier origins of HSCs in the aorta-gonadsmesonephros (AGM).…”
Section: Introductionmentioning
confidence: 99%