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Jean-Pierre Levesque

Researcher at University of Queensland

Publications -  185
Citations -  9865

Jean-Pierre Levesque is an academic researcher from University of Queensland. The author has contributed to research in topics: Bone marrow & Haematopoiesis. The author has an hindex of 48, co-authored 177 publications receiving 9070 citations. Previous affiliations of Jean-Pierre Levesque include University of Illinois at Chicago & Washington University in St. Louis.

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Disruption of the CXCR4/CXCL12 chemotactic interaction during hematopoietic stem cell mobilization induced by GCSF or cyclophosphamide.

TL;DR: It is reported that mobilization of HPCs by GCSF coincides in vivo with the cleavage of the N-terminus of the chemokine receptor CXCR4 on H PCs resident in the BM and mobilized into the PB.
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Bone marrow macrophages maintain hematopoietic stem cell (HSC) niches and their depletion mobilizes HSCs

TL;DR: It is established that bone marrow macrophages are pivotal to maintain the endosteal HSC niche and that the loss of such macrophage leads to the egress of HSCs into the blood.
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Vascular cell adhesion molecule-1 (CD106) is cleaved by neutrophil proteases in the bone marrow following hematopoietic progenitor cell mobilization by granulocyte colony-stimulating factor

TL;DR: It is made that an essential step contributing to the mobilization of HPCs is the proteolytic cleavage of VCAM-1 expressed by BM stromal cells, an event triggered by the degranulation of neutrophils accumulating in the BM in response to the administration of G-CSF.
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G-CSF potently inhibits osteoblast activity and CXCL12 mRNA expression in the bone marrow

TL;DR: Data suggest a model in which G-CSF, through an indirect mechanism, potently inhibits osteoblast activity resulting in decreased CXCL12 expression in the bone marrow, which ultimately leads to HPC mobilization.
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Vascular niche E-selectin regulates hematopoietic stem cell dormancy, self renewal and chemoresistance

TL;DR: A new role for the adhesion molecule E-selectin expressed exclusively by bone marrow endothelial cells in the vascular HSC niche is reported, demonstrating that E- selectin promotes HSC proliferation and is a crucial component of the vascular niche.