Author
Listed:
- Jonathan Hoggatt
(Microbiology and Immunology, Indiana University School of Medicine
Stem Cell and Regenerative Biology, Harvard University/Harvard Stem Cell Institute/Harvard Medical School/Center for Regenerative Medicine, Massachusetts General Hospital)
- Khalid S. Mohammad
(Medicine/Endocrinology, Indiana University School of Medicine)
- Pratibha Singh
(Microbiology and Immunology, Indiana University School of Medicine)
- Amber F. Hoggatt
(Microbiology and Immunology, Indiana University School of Medicine
Biologic Resources Laboratory, University of Illinois at Chicago)
- Brahmananda R. Chitteti
(Indiana University School of Medicine)
- Jennifer M. Speth
(Microbiology and Immunology, Indiana University School of Medicine)
- Peirong Hu
(Microbiology and Immunology, Indiana University School of Medicine)
- Bradley A. Poteat
(Indiana University School of Medicine)
- Kayla N. Stilger
(Microbiology and Immunology, Indiana University School of Medicine)
- Francesca Ferraro
(Stem Cell and Regenerative Biology, Harvard University/Harvard Stem Cell Institute/Harvard Medical School/Center for Regenerative Medicine, Massachusetts General Hospital)
- Lev Silberstein
(Stem Cell and Regenerative Biology, Harvard University/Harvard Stem Cell Institute/Harvard Medical School/Center for Regenerative Medicine, Massachusetts General Hospital)
- Frankie K. Wong
(Stem Cell and Regenerative Biology, Harvard University/Harvard Stem Cell Institute/Harvard Medical School/Center for Regenerative Medicine, Massachusetts General Hospital)
- Sherif S. Farag
(Indiana University School of Medicine)
- Magdalena Czader
(Pathology and Laboratory Medicine, Indiana University School of Medicine)
- Ginger L. Milne
(Eicosanoid Core Laboratory, Vanderbilt University)
- Richard M. Breyer
(Vanderbilt University)
- Carlos H. Serezani
(Microbiology and Immunology, Indiana University School of Medicine)
- David T. Scadden
(Stem Cell and Regenerative Biology, Harvard University/Harvard Stem Cell Institute/Harvard Medical School/Center for Regenerative Medicine, Massachusetts General Hospital)
- Theresa A. Guise
(Medicine/Endocrinology, Indiana University School of Medicine)
- Edward F. Srour
(Microbiology and Immunology, Indiana University School of Medicine
Indiana University School of Medicine)
- Louis M. Pelus
(Microbiology and Immunology, Indiana University School of Medicine)
Abstract
Endogenous prostaglandin E2 (PGE2) is a potent regulator of haematopoietic stem cell (HSC) retention in the bone marrow; inhibition of endogenous PGE2 signalling by non-steroidal anti-inflammatory drugs results in enhanced HSC and haematopoietic progenitor cell mobility via E-prostanoid 4 (EP4) receptor antagonism.
Suggested Citation
Jonathan Hoggatt & Khalid S. Mohammad & Pratibha Singh & Amber F. Hoggatt & Brahmananda R. Chitteti & Jennifer M. Speth & Peirong Hu & Bradley A. Poteat & Kayla N. Stilger & Francesca Ferraro & Lev Si, 2013.
"Differential stem- and progenitor-cell trafficking by prostaglandin E2,"
Nature, Nature, vol. 495(7441), pages 365-369, March.
Handle:
RePEc:nat:nature:v:495:y:2013:i:7441:d:10.1038_nature11929
DOI: 10.1038/nature11929
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