دورية أكاديمية
Endothelial Cell Indoleamine 2, 3-Dioxygenase 1 Alters Cardiac Function After Myocardial Infarction Through Kynurenine.
| العنوان: | Endothelial Cell Indoleamine 2, 3-Dioxygenase 1 Alters Cardiac Function After Myocardial Infarction Through Kynurenine. |
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| المؤلفون: | Melhem, Nada Joe, Chajadine, Mouna, Gomez, Ingrid, Howangyin, Kiave-Yune, Bouvet, Marion, Knosp, Camille, Sun, Yanyi, Rouanet, Marie, Laurans, Ludivine, Cazorla, Olivier, Lemitre, Mathilde, Vilar, José, Mallat, Ziad, Tedgui, Alain, Ait-Oufella, Hafid, Hulot, Jean-Sébastien, Callebert, Jacques, Launay, Jean-Marie, Fauconnier, Jeremy, Silvestre, Jean-Sébastien, Taleb, Soraya |
| بيانات النشر: | Ovid Technologies (Wolters Kluwer Health) //dx.doi.org/10.1161/circulationaha.120.050301 Circulation |
| سنة النشر: | 2021 |
| المجموعة: | Apollo - University of Cambridge Repository |
| مصطلحات موضوعية: | IDO, apoptosis, kynurenine, myocardial infarction, tryptophan, Animals, Endothelial Cells, Humans, Indoleamine-Pyrrole 2,3,-Dioxygenase, Mice |
| الوصف: | BACKGROUND: Ischemic cardiovascular diseases, particularly acute myocardial infarction (MI), is one of the leading causes of mortality worldwide. Indoleamine 2, 3-dioxygenase 1 (IDO) catalyzes 1 rate-limiting step of L-tryptophan metabolism, and emerges as an important regulator of many pathological conditions. We hypothesized that IDO could play a key role to locally regulate cardiac homeostasis after MI. METHODS: Cardiac repair was analyzed in mice harboring specific endothelial or smooth muscle cells or cardiomyocyte or myeloid cell deficiency of IDO and challenged with acute myocardial infarction. RESULTS: We show that kynurenine generation through IDO is markedly induced after MI in mice. Total genetic deletion or pharmacological inhibition of IDO limits cardiac injury and cardiac dysfunction after MI. Distinct loss of function of IDO in smooth muscle cells, inflammatory cells, or cardiomyocytes does not affect cardiac function and remodeling in infarcted mice. In sharp contrast, mice harboring endothelial cell-specific deletion of IDO show an improvement of cardiac function as well as cardiomyocyte contractility and reduction in adverse ventricular remodeling. In vivo kynurenine supplementation in IDO-deficient mice abrogates the protective effects of IDO deletion. Kynurenine precipitates cardiomyocyte apoptosis through reactive oxygen species production in an aryl hydrocarbon receptor-dependent mechanism. CONCLUSIONS: These data suggest that IDO could constitute a new therapeutic target during acute MI. |
| نوع الوثيقة: | article in journal/newspaper |
| وصف الملف: | Print-Electronic; application/pdf |
| اللغة: | English |
| العلاقة: | https://www.repository.cam.ac.uk/handle/1810/314866Test |
| DOI: | 10.17863/CAM.61972 |
| الإتاحة: | https://doi.org/10.17863/CAM.61972Test https://www.repository.cam.ac.uk/handle/1810/314866Test |
| حقوق: | All rights reserved |
| رقم الانضمام: | edsbas.D8115485 |
| قاعدة البيانات: | BASE |
| DOI: | 10.17863/CAM.61972 |
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