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Cardio-omentopexy requires a cardioprotective innate immune response to promote myocardial angiogenesis in mice
OBJECTIVE: The pedicled greater omentum, when applied onto stressed hearts using omentopexy, has been shown to be protective in humans and animals. The mechanisms underlying cardioprotection using omentopexy remain elusive. This study examined whether macrophage-mediated angiogenesis accounts for th...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9390370/ https://www.ncbi.nlm.nih.gov/pubmed/36004249 http://dx.doi.org/10.1016/j.xjon.2022.02.027 |
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author | Ge, Zhi-Dong Boyd, Riley M. Lantz, Connor Thorp, Edward B. Forbess, Joseph M. |
author_facet | Ge, Zhi-Dong Boyd, Riley M. Lantz, Connor Thorp, Edward B. Forbess, Joseph M. |
author_sort | Ge, Zhi-Dong |
collection | PubMed |
description | OBJECTIVE: The pedicled greater omentum, when applied onto stressed hearts using omentopexy, has been shown to be protective in humans and animals. The mechanisms underlying cardioprotection using omentopexy remain elusive. This study examined whether macrophage-mediated angiogenesis accounts for the cardioprotective effect of omentopexy in mice. METHODS: C57BL/6 mice were subjected to minimally invasive transverse aortic constriction for 6 weeks and subsequent cardio-omentopexy for 8 weeks. Control mice underwent the same surgical procedures without aortic constriction or cardio-omentopexy. RESULTS: Transverse aortic constriction led to left ventricular concentric hypertrophy, reduced mitral E/A ratio, increased cardiomyocyte size, and myocardial fibrosis in the mice that underwent sham cardio-omentopexy surgery. The negative effects of transverse aortic constriction were prevented by cardio-omentopexy. Myocardial microvessel density was elevated in the mice that underwent aortic constriction and sham cardio-omentopexy surgery, and cardio-omentopexy further enhanced angiogenesis. Nanostring gene array analysis uncovered the activation of angiogenesis gene networks by cardio-omentopexy. Flow cytometric analysis revealed that cardio-omentopexy triggered the accumulation of cardiac MHCII(lo)Lyve1+TimD4+ (Major histocompatibility complex class II(low) lymphatic vessel endothelial hyaluronan receptor 1+ T cell immunoglobulin and mucin domain conataining 4+) resident macrophages at the omental–cardiac interface. Intriguingly, the depletion of macrophages with clodronate-liposome resulted in the failure of cardio-omentopexy to protect the heart and promote angiogenesis. CONCLUSIONS: Cardio-omentopexy protects the heart from pressure overload-elicited left ventricular hypertrophy and dysfunction by promoting myocardial angiogenesis. Cardiac MHCII(lo)Lyve1+TimD4+ resident macrophages play a critical role in the cardioprotective effect and angiogenesis of cardio-omentopexy. VIDEO ABSTRACT: |
format | Online Article Text |
id | pubmed-9390370 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-93903702022-08-23 Cardio-omentopexy requires a cardioprotective innate immune response to promote myocardial angiogenesis in mice Ge, Zhi-Dong Boyd, Riley M. Lantz, Connor Thorp, Edward B. Forbess, Joseph M. JTCVS Open Adult: Coronary: Basic Science OBJECTIVE: The pedicled greater omentum, when applied onto stressed hearts using omentopexy, has been shown to be protective in humans and animals. The mechanisms underlying cardioprotection using omentopexy remain elusive. This study examined whether macrophage-mediated angiogenesis accounts for the cardioprotective effect of omentopexy in mice. METHODS: C57BL/6 mice were subjected to minimally invasive transverse aortic constriction for 6 weeks and subsequent cardio-omentopexy for 8 weeks. Control mice underwent the same surgical procedures without aortic constriction or cardio-omentopexy. RESULTS: Transverse aortic constriction led to left ventricular concentric hypertrophy, reduced mitral E/A ratio, increased cardiomyocyte size, and myocardial fibrosis in the mice that underwent sham cardio-omentopexy surgery. The negative effects of transverse aortic constriction were prevented by cardio-omentopexy. Myocardial microvessel density was elevated in the mice that underwent aortic constriction and sham cardio-omentopexy surgery, and cardio-omentopexy further enhanced angiogenesis. Nanostring gene array analysis uncovered the activation of angiogenesis gene networks by cardio-omentopexy. Flow cytometric analysis revealed that cardio-omentopexy triggered the accumulation of cardiac MHCII(lo)Lyve1+TimD4+ (Major histocompatibility complex class II(low) lymphatic vessel endothelial hyaluronan receptor 1+ T cell immunoglobulin and mucin domain conataining 4+) resident macrophages at the omental–cardiac interface. Intriguingly, the depletion of macrophages with clodronate-liposome resulted in the failure of cardio-omentopexy to protect the heart and promote angiogenesis. CONCLUSIONS: Cardio-omentopexy protects the heart from pressure overload-elicited left ventricular hypertrophy and dysfunction by promoting myocardial angiogenesis. Cardiac MHCII(lo)Lyve1+TimD4+ resident macrophages play a critical role in the cardioprotective effect and angiogenesis of cardio-omentopexy. VIDEO ABSTRACT: Elsevier 2022-02-24 /pmc/articles/PMC9390370/ /pubmed/36004249 http://dx.doi.org/10.1016/j.xjon.2022.02.027 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Adult: Coronary: Basic Science Ge, Zhi-Dong Boyd, Riley M. Lantz, Connor Thorp, Edward B. Forbess, Joseph M. Cardio-omentopexy requires a cardioprotective innate immune response to promote myocardial angiogenesis in mice |
title | Cardio-omentopexy requires a cardioprotective innate immune response to promote myocardial angiogenesis in mice |
title_full | Cardio-omentopexy requires a cardioprotective innate immune response to promote myocardial angiogenesis in mice |
title_fullStr | Cardio-omentopexy requires a cardioprotective innate immune response to promote myocardial angiogenesis in mice |
title_full_unstemmed | Cardio-omentopexy requires a cardioprotective innate immune response to promote myocardial angiogenesis in mice |
title_short | Cardio-omentopexy requires a cardioprotective innate immune response to promote myocardial angiogenesis in mice |
title_sort | cardio-omentopexy requires a cardioprotective innate immune response to promote myocardial angiogenesis in mice |
topic | Adult: Coronary: Basic Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9390370/ https://www.ncbi.nlm.nih.gov/pubmed/36004249 http://dx.doi.org/10.1016/j.xjon.2022.02.027 |
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