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Macrophage efferocytosis with VEGFC and lymphangiogenesis: rescuing the broken heart

Cardiac repair following ischemic injury is indispensable for survival and requires a coordinated cellular response involving the mobilization of immune cells from the secondary lymphoid organs to the site of damage. Efferocytosis, the engulfment of cell debris and dying cells by innate immune cells...

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Detalles Bibliográficos
Autores principales: D’Amore, Patricia A., Alcaide, Pilar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Clinical Investigation 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9057620/
https://www.ncbi.nlm.nih.gov/pubmed/35499075
http://dx.doi.org/10.1172/JCI158703
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author D’Amore, Patricia A.
Alcaide, Pilar
author_facet D’Amore, Patricia A.
Alcaide, Pilar
author_sort D’Amore, Patricia A.
collection PubMed
description Cardiac repair following ischemic injury is indispensable for survival and requires a coordinated cellular response involving the mobilization of immune cells from the secondary lymphoid organs to the site of damage. Efferocytosis, the engulfment of cell debris and dying cells by innate immune cells, along with lymphangiogenesis, the formation of new lymphatic vessels, are emerging as central to the cardiac healing response. In this issue of the JCI, Glinton et al. used state-of-the-art approaches to demonstrate that efferocytosis induced vascular endothelial growth factor C (VEGFC) in myeloid cells and stimulated lymphangiogenesis and cardiac repair. These findings provide impactful mechanistic information that can be leveraged to therapeutically target pathways in cardiac repair and ischemic heart failure.
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spelling pubmed-90576202022-05-04 Macrophage efferocytosis with VEGFC and lymphangiogenesis: rescuing the broken heart D’Amore, Patricia A. Alcaide, Pilar J Clin Invest Commentary Cardiac repair following ischemic injury is indispensable for survival and requires a coordinated cellular response involving the mobilization of immune cells from the secondary lymphoid organs to the site of damage. Efferocytosis, the engulfment of cell debris and dying cells by innate immune cells, along with lymphangiogenesis, the formation of new lymphatic vessels, are emerging as central to the cardiac healing response. In this issue of the JCI, Glinton et al. used state-of-the-art approaches to demonstrate that efferocytosis induced vascular endothelial growth factor C (VEGFC) in myeloid cells and stimulated lymphangiogenesis and cardiac repair. These findings provide impactful mechanistic information that can be leveraged to therapeutically target pathways in cardiac repair and ischemic heart failure. American Society for Clinical Investigation 2022-05-02 2022-05-02 /pmc/articles/PMC9057620/ /pubmed/35499075 http://dx.doi.org/10.1172/JCI158703 Text en © 2022 D’Amore et al. https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Commentary
D’Amore, Patricia A.
Alcaide, Pilar
Macrophage efferocytosis with VEGFC and lymphangiogenesis: rescuing the broken heart
title Macrophage efferocytosis with VEGFC and lymphangiogenesis: rescuing the broken heart
title_full Macrophage efferocytosis with VEGFC and lymphangiogenesis: rescuing the broken heart
title_fullStr Macrophage efferocytosis with VEGFC and lymphangiogenesis: rescuing the broken heart
title_full_unstemmed Macrophage efferocytosis with VEGFC and lymphangiogenesis: rescuing the broken heart
title_short Macrophage efferocytosis with VEGFC and lymphangiogenesis: rescuing the broken heart
title_sort macrophage efferocytosis with vegfc and lymphangiogenesis: rescuing the broken heart
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9057620/
https://www.ncbi.nlm.nih.gov/pubmed/35499075
http://dx.doi.org/10.1172/JCI158703
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