Platelet neuropeptide Y is critical for ischemic revascularization in mice.

MedStar author(s):
Citation: FASEB Journal. 27(6):2244-55, 2013 Jun.PMID: 23457218Institution: MedStar Health Research InstituteForm of publication: Journal ArticleMedline article type(s): Journal Article | Research Support, N.I.H., ExtramuralSubject headings: *Blood Platelets/me [Metabolism] | *Ischemia/bl [Blood] | *Neovascularization, Physiologic | *Neuropeptide Y/ph [Physiology] | Animals | Cell Proliferation | Cells, Cultured | Disease Models, Animal | Endothelial Cells/pa [Pathology] | Hindlimb | Humans | Ischemia/ge [Genetics] | Ischemia/pp [Physiopathology] | Male | Mice | Mice, 129 Strain | Mice, Knockout | Neovascularization, Physiologic/ge [Genetics] | Neuropeptide Y/df [Deficiency] | Neuropeptide Y/ge [Genetics] | Rats | Rats, WistarYear: 2013Local holdings: Available online from MWHC library: July 1987 - present (after 1 year)ISSN:
  • 0892-6638
Name of journal: FASEB journal : official publication of the Federation of American Societies for Experimental BiologyAbstract: We previously reported that the sympathetic neurotransmitter neuropeptide Y (NPY) is potently angiogenic, primarily through its Y2 receptor, and that endogenous NPY is crucial for capillary angiogenesis in rodent hindlimb ischemia. Here we sought to identify the source of NPY responsible for revascularization and its mechanisms of action. At d 3, NPY(-/-) mice demonstrated delayed recovery of blood flow and limb function, consistent with impaired collateral conductance, while ischemic capillary angiogenesis was reduced (~70%) at d 14. This biphasic temporal response was confirmed by 2 peaks of NPY activation in rats: a transient early increase in neuronally derived plasma NPY and increase in platelet NPY during late-phase recovery. Compared to NPY-null platelets, collagen-activated NPY-rich platelets were more mitogenic (~2-fold vs. ~1.6-fold increase) for human microvascular endothelial cells, and Y2/Y5 receptor antagonists ablated this difference in proliferation. In NPY(+/+) mice, ischemic angiogenesis was prevented by platelet depletion and then restored by transfusion of platelets from NPY(+/+) mice, but not NPY(-/-) mice. In thrombocytopenic NPY(-/-) mice, transfusion of wild-type platelets fully restored ischemia-induced angiogenesis. These findings suggest that neuronally derived NPY accelerates the early response to femoral artery ligation by promoting collateral conductance, while platelet-derived NPY is critical for sustained capillary angiogenesis.All authors: Abe K, Burnett MS, Chalothorn D, Epstein SE, Everhart LM, Faber JE, Kitlinska J, Kuo-Bonde L, Tilan JU, Zukowska ZFiscal year: FY2013Digital Object Identifier: Date added to catalog: 2013-09-17
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Journal Article MedStar Authors Catalog Article 23457218 Available 23457218

Available online from MWHC library: July 1987 - present (after 1 year)

We previously reported that the sympathetic neurotransmitter neuropeptide Y (NPY) is potently angiogenic, primarily through its Y2 receptor, and that endogenous NPY is crucial for capillary angiogenesis in rodent hindlimb ischemia. Here we sought to identify the source of NPY responsible for revascularization and its mechanisms of action. At d 3, NPY(-/-) mice demonstrated delayed recovery of blood flow and limb function, consistent with impaired collateral conductance, while ischemic capillary angiogenesis was reduced (~70%) at d 14. This biphasic temporal response was confirmed by 2 peaks of NPY activation in rats: a transient early increase in neuronally derived plasma NPY and increase in platelet NPY during late-phase recovery. Compared to NPY-null platelets, collagen-activated NPY-rich platelets were more mitogenic (~2-fold vs. ~1.6-fold increase) for human microvascular endothelial cells, and Y2/Y5 receptor antagonists ablated this difference in proliferation. In NPY(+/+) mice, ischemic angiogenesis was prevented by platelet depletion and then restored by transfusion of platelets from NPY(+/+) mice, but not NPY(-/-) mice. In thrombocytopenic NPY(-/-) mice, transfusion of wild-type platelets fully restored ischemia-induced angiogenesis. These findings suggest that neuronally derived NPY accelerates the early response to femoral artery ligation by promoting collateral conductance, while platelet-derived NPY is critical for sustained capillary angiogenesis.

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