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Epoxyeicosanoids promote organ and tissue regeneration
by
D'Amore, Patricia A.
, Ingber, Donald E.
, Kalish, Brian T.
, Jenkins, Roger L.
, Inceoglu, Bora
, Butterfield, Catherine E.
, Kieran, Mark W.
, Simpson, Mary A.
, Lee, Craig R.
, Manthati, Vijaya L.
, Tomer, Kenneth B.
, Kaipainen, Arja
, Lih, Fred B.
, Bielenberg, Diane R.
, Panigrahy, Dipak
, Yang, Jun
, Mammoto, Tadanori
, Le, Hau D.
, Huang, Sui
, Mudge, Dayna K.
, Falck, John R.
, Zeldin, Darryl C.
, Puder, Mark
, Edin, Matthew L.
, Akino, Tomoshige
, Mammoto, Akiko
, Benny, Ofra
, Hammock, Bruce D.
in
acids
/ Angiogenesis
/ Animals
/ Biological activity
/ Biological Sciences
/ Chromatography, Liquid
/ compensatory growth
/ cornea
/ cytochrome P-450
/ Eicosanoids - metabolism
/ Eicosanoids - pharmacology
/ endothelial cells
/ Endothelial Cells - metabolism
/ Endothelium
/ epoxide hydrolase
/ Epoxide Hydrolases - antagonists & inhibitors
/ Epoxy Compounds - metabolism
/ Epoxy Compounds - pharmacology
/ Eye - blood supply
/ Genetics
/ Growth factors
/ Hepatectomy
/ Hepatocytes
/ Homeostasis
/ Immunohistochemistry
/ inflammation
/ Kidney - physiology
/ Kidneys
/ lipids
/ Liver
/ Liver - physiology
/ Liver regeneration
/ Lung - physiology
/ Lungs
/ Mice
/ Mice, Transgenic
/ Neovascularization, Physiologic - drug effects
/ Neovascularization, Physiologic - physiology
/ Pharmacology
/ Physiology
/ pleiotropy
/ Receptor, TIE-2 - genetics
/ Regeneration
/ Regeneration - drug effects
/ Regeneration - physiology
/ Tandem Mass Spectrometry
/ Tissue engineering
/ tissue repair
/ Tissues
/ Wound healing
2013
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Epoxyeicosanoids promote organ and tissue regeneration
by
D'Amore, Patricia A.
, Ingber, Donald E.
, Kalish, Brian T.
, Jenkins, Roger L.
, Inceoglu, Bora
, Butterfield, Catherine E.
, Kieran, Mark W.
, Simpson, Mary A.
, Lee, Craig R.
, Manthati, Vijaya L.
, Tomer, Kenneth B.
, Kaipainen, Arja
, Lih, Fred B.
, Bielenberg, Diane R.
, Panigrahy, Dipak
, Yang, Jun
, Mammoto, Tadanori
, Le, Hau D.
, Huang, Sui
, Mudge, Dayna K.
, Falck, John R.
, Zeldin, Darryl C.
, Puder, Mark
, Edin, Matthew L.
, Akino, Tomoshige
, Mammoto, Akiko
, Benny, Ofra
, Hammock, Bruce D.
in
acids
/ Angiogenesis
/ Animals
/ Biological activity
/ Biological Sciences
/ Chromatography, Liquid
/ compensatory growth
/ cornea
/ cytochrome P-450
/ Eicosanoids - metabolism
/ Eicosanoids - pharmacology
/ endothelial cells
/ Endothelial Cells - metabolism
/ Endothelium
/ epoxide hydrolase
/ Epoxide Hydrolases - antagonists & inhibitors
/ Epoxy Compounds - metabolism
/ Epoxy Compounds - pharmacology
/ Eye - blood supply
/ Genetics
/ Growth factors
/ Hepatectomy
/ Hepatocytes
/ Homeostasis
/ Immunohistochemistry
/ inflammation
/ Kidney - physiology
/ Kidneys
/ lipids
/ Liver
/ Liver - physiology
/ Liver regeneration
/ Lung - physiology
/ Lungs
/ Mice
/ Mice, Transgenic
/ Neovascularization, Physiologic - drug effects
/ Neovascularization, Physiologic - physiology
/ Pharmacology
/ Physiology
/ pleiotropy
/ Receptor, TIE-2 - genetics
/ Regeneration
/ Regeneration - drug effects
/ Regeneration - physiology
/ Tandem Mass Spectrometry
/ Tissue engineering
/ tissue repair
/ Tissues
/ Wound healing
2013
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Epoxyeicosanoids promote organ and tissue regeneration
by
D'Amore, Patricia A.
, Ingber, Donald E.
, Kalish, Brian T.
, Jenkins, Roger L.
, Inceoglu, Bora
, Butterfield, Catherine E.
, Kieran, Mark W.
, Simpson, Mary A.
, Lee, Craig R.
, Manthati, Vijaya L.
, Tomer, Kenneth B.
, Kaipainen, Arja
, Lih, Fred B.
, Bielenberg, Diane R.
, Panigrahy, Dipak
, Yang, Jun
, Mammoto, Tadanori
, Le, Hau D.
, Huang, Sui
, Mudge, Dayna K.
, Falck, John R.
, Zeldin, Darryl C.
, Puder, Mark
, Edin, Matthew L.
, Akino, Tomoshige
, Mammoto, Akiko
, Benny, Ofra
, Hammock, Bruce D.
in
acids
/ Angiogenesis
/ Animals
/ Biological activity
/ Biological Sciences
/ Chromatography, Liquid
/ compensatory growth
/ cornea
/ cytochrome P-450
/ Eicosanoids - metabolism
/ Eicosanoids - pharmacology
/ endothelial cells
/ Endothelial Cells - metabolism
/ Endothelium
/ epoxide hydrolase
/ Epoxide Hydrolases - antagonists & inhibitors
/ Epoxy Compounds - metabolism
/ Epoxy Compounds - pharmacology
/ Eye - blood supply
/ Genetics
/ Growth factors
/ Hepatectomy
/ Hepatocytes
/ Homeostasis
/ Immunohistochemistry
/ inflammation
/ Kidney - physiology
/ Kidneys
/ lipids
/ Liver
/ Liver - physiology
/ Liver regeneration
/ Lung - physiology
/ Lungs
/ Mice
/ Mice, Transgenic
/ Neovascularization, Physiologic - drug effects
/ Neovascularization, Physiologic - physiology
/ Pharmacology
/ Physiology
/ pleiotropy
/ Receptor, TIE-2 - genetics
/ Regeneration
/ Regeneration - drug effects
/ Regeneration - physiology
/ Tandem Mass Spectrometry
/ Tissue engineering
/ tissue repair
/ Tissues
/ Wound healing
2013
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Journal Article
Epoxyeicosanoids promote organ and tissue regeneration
2013
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Overview
Epoxyeicosatrienoic acids (EETs), lipid mediators produced by cytochrome P450 epoxygenases, regulate inflammation, angiogenesis, and vascular tone. Despite pleiotropic effects on cells, the role of these epoxyeicosanoids in normal organ and tissue regeneration remains unknown. EETs are produced predominantly in the endothelium. Normal organ and tissue regeneration require an active paracrine role of the microvascular endothelium, which in turn depends on angiogenic growth factors. Thus, we hypothesize that endothelial cells stimulate organ and tissue regeneration via production of bioactive EETs. To determine whether endothelial-derived EETs affect physiologic tissue growth in vivo, we used genetic and pharmacological tools to manipulate endogenous EET levels. We show that endothelial-derived EETs play a critical role in accelerating tissue growth in vivo, including liver regeneration, kidney compensatory growth, lung compensatory growth, wound healing, corneal neovascularization, and retinal vascularization. Administration of synthetic EETs recapitulated these results, whereas lowering EET levels, either genetically or pharmacologically, delayed tissue regeneration, demonstrating that pharmacological modulation of EETs can affect normal organ and tissue growth. We also show that soluble epoxide hydrolase inhibitors, which elevate endogenous EET levels, promote liver and lung regeneration. Thus, our observations indicate a central role for EETs in organ and tissue regeneration and their contribution to tissue homeostasis.
Publisher
National Academy of Sciences,National Acad Sciences
Subject
/ Animals
/ cornea
/ Endothelial Cells - metabolism
/ Epoxide Hydrolases - antagonists & inhibitors
/ Epoxy Compounds - metabolism
/ Epoxy Compounds - pharmacology
/ Genetics
/ Kidneys
/ lipids
/ Liver
/ Lungs
/ Mice
/ Neovascularization, Physiologic - drug effects
/ Neovascularization, Physiologic - physiology
/ Tissues
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