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Endothelial β1 Integrin-Mediated Adaptation to Myocardial Ischemia.
- Source :
-
Thrombosis and haemostasis [Thromb Haemost] 2021 Jun; Vol. 121 (6), pp. 741-754. Date of Electronic Publication: 2021 Jan 14. - Publication Year :
- 2021
-
Abstract
- Background: Short episodes of myocardial ischemia can protect from myocardial infarction. However, the role of endothelial β1 integrin in these cardioprotective ischemic events is largely unknown.<br />Objective: In this study we investigated whether endothelial β1 integrin is required for cardiac adaptation to ischemia and protection from myocardial infarction.<br />Methods: Here we introduced transient and permanent left anterior descending artery (LAD) occlusions in mice. We inhibited β1 integrin by intravenous injection of function-blocking antibodies and tamoxifen-induced endothelial cell (EC)-specific deletion of Itgb1 . Furthermore, human ITGB1 was silenced in primary human coronary artery ECs using small interfering RNA. We analyzed the numbers of proliferating ECs and arterioles by immunohistochemistry, determined infarct size by magnetic resonance imaging (MRI) and triphenyl tetrazolium chloride staining, and analyzed cardiac function by MRI and echocardiography.<br />Results: Transient LAD occlusions were found to increase EC proliferation and arteriole formation in the entire myocardium. These effects required β1 integrin on ECs, except for arteriole formation in the ischemic part of the myocardium. Furthermore, this integrin subunit was also relevant for basal and mechanically induced proliferation of human coronary artery ECs. Notably, β1 integrin was needed for cardioprotection induced by transient LAD occlusions, and the absence of endothelial β1 integrin resulted in impaired growth of blood vessels into the infarcted myocardium and reduced cardiac function after permanent LAD occlusion.<br />Conclusion: We showed that endothelial β1 integrin is required for adaptation of the heart to cardiac ischemia and protection from myocardial infarction.<br />Competing Interests: None declared.<br /> (The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/).)
- Subjects :
- Animals
Cell Proliferation
Coronary Vessels pathology
Disease Models, Animal
Endothelial Cells pathology
Humans
Integrin beta1 genetics
Male
Mice, Inbred C57BL
Mice, Knockout
Myocardial Infarction genetics
Myocardial Infarction metabolism
Myocardial Infarction pathology
Neovascularization, Physiologic
Nitric Oxide Synthase Type III genetics
Nitric Oxide Synthase Type III metabolism
Signal Transduction
Young Adult
Mice
Coronary Vessels metabolism
Endothelial Cells metabolism
Integrin beta1 metabolism
Ischemic Preconditioning, Myocardial
Myocardial Infarction prevention & control
Subjects
Details
- Language :
- English
- ISSN :
- 2567-689X
- Volume :
- 121
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Thrombosis and haemostasis
- Publication Type :
- Academic Journal
- Accession number :
- 33469904
- Full Text :
- https://doi.org/10.1055/s-0040-1721505