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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/11559
Title: Acute erythropoietin cardioprotection is mediated by endothelial response
Authors: Ruifeng Teng
John W. Calvert
Nathawut Sibmooh
Barbora Piknova
Norio Suzuki
Junhui Sun
Kevin Martinez
Masayuki Yamamoto
Alan N. Schechter
David J. Lefer
Constance Tom Noguchi
National Institute of Diabetes and Digestive and Kidney Diseases
Emory University School of Medicine
Mahidol University
Tohoku University School of Medicine
National Heart, Lung, and Blood Institute
Keywords: Biochemistry, Genetics and Molecular Biology;Medicine
Issue Date: 1-May-2011
Citation: Basic Research in Cardiology. Vol.106, No.3 (2011), 343-354
Abstract: Increasing evidence indicates that high levels of serum erythropoietin (Epo) can lessen ischemia-reperfusion injury in the heart and multiple cardiac cell types have been suggested to play a role in this Epo effect. To clarify the mechanisms underlying this cardioprotection, we explored Epo treatment of coronary artery endothelial cells and Epo cardioprotection in a Mus musculus model with Epo receptor expression restricted to hematopoietic and endothelial cells (ΔEpoR). Epo stimulation of coronary artery endothelial cells upregulated endothelial nitric oxide synthase (eNOS) activity in vitro and in vivo, and enhanced nitric oxide (NO) production that was determined directly by real-time measurements of gaseous NO release. Epo stimulated phosphoinositide 3-kinase (PI3K)/protein kinase B (AKT) and mitogen-activated protein kinase kinase (MEK)/extracellular signal regulated kinase (ERK) signaling pathways, and inhibition of PI3K, but not MEK activity, blocked Epo-induced NO production. To verify the potential of this Epo effect in cardioprotection in vivo, ΔEpoR-mice with Epo response in heart restricted to endothelium were treated with Epo. These mice exhibited a similar increase in eNOS phosphorylation in coronary artery endothelium as that found in wild type (WT) mice. In addition, in both WT- and ΔEpoR-mice, exogenous Epo treatment prior to myocardial ischemia provided comparable protection. These data provide the first evidence that endothelial cell response to Epo is sufficient to achieve an acute cardioprotective effect. The immediate response of coronary artery endothelial cells to Epo stimulation by NO production may be a critical mechanism underlying this Epo cardioprotection. © 2011 Springer-Verlag (outside the USA).
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=79955534586&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/11559
ISSN: 14351803
03008428
Appears in Collections:Scopus 2011-2015

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