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PHD2 regulates arteriogenic macrophages through TIE2 signalling
Occlusion of the main arterial route redirects blood flow to the collateral circulation. We previously reported that macrophages genetically modified to express low levels of prolyl hydroxylase domain protein 2 (PHD2) display an arteriogenic phenotype, which promotes the formation of collateral vess...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
WILEY-VCH Verlag
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3779447/ https://www.ncbi.nlm.nih.gov/pubmed/23616286 http://dx.doi.org/10.1002/emmm.201302695 |
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author | Hamm, Alexander Veschini, Lorenzo Takeda, Yukiji Costa, Sandra Delamarre, Estelle Squadrito, Mario Leonardo Henze, Anne-Theres Wenes, Mathias Serneels, Jens Pucci, Ferdinando Roncal, Carmen Anisimov, Andrey Alitalo, Kari De Palma, Michele Mazzone, Massimiliano |
author_facet | Hamm, Alexander Veschini, Lorenzo Takeda, Yukiji Costa, Sandra Delamarre, Estelle Squadrito, Mario Leonardo Henze, Anne-Theres Wenes, Mathias Serneels, Jens Pucci, Ferdinando Roncal, Carmen Anisimov, Andrey Alitalo, Kari De Palma, Michele Mazzone, Massimiliano |
author_sort | Hamm, Alexander |
collection | PubMed |
description | Occlusion of the main arterial route redirects blood flow to the collateral circulation. We previously reported that macrophages genetically modified to express low levels of prolyl hydroxylase domain protein 2 (PHD2) display an arteriogenic phenotype, which promotes the formation of collateral vessels and protects the skeletal muscle from ischaemic necrosis. However, the molecular mechanisms underlying this process are unknown. Here, we demonstrate that femoral artery occlusion induces a switch in macrophage phenotype through angiopoietin-1 (ANG1)-mediated Phd2 repression. ANG blockade by a soluble trap prevented the downregulation of Phd2 expression in macrophages and their phenotypic switch, thus inhibiting collateral growth. ANG1-dependent Phd2 repression initiated a feed-forward loop mediated by the induction of the ANG receptor TIE2 in macrophages. Gene silencing and cell depletion strategies demonstrate that TIE2 induction in macrophages is required to promote their proarteriogenic functions, enabling collateral vessel formation following arterial obstruction. These results indicate an indispensable role for TIE2 in sustaining in situ programming of macrophages to a proarteriogenic, M2-like phenotype, suggesting possible new venues for the treatment of ischaemic disorders. |
format | Online Article Text |
id | pubmed-3779447 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | WILEY-VCH Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-37794472013-09-23 PHD2 regulates arteriogenic macrophages through TIE2 signalling Hamm, Alexander Veschini, Lorenzo Takeda, Yukiji Costa, Sandra Delamarre, Estelle Squadrito, Mario Leonardo Henze, Anne-Theres Wenes, Mathias Serneels, Jens Pucci, Ferdinando Roncal, Carmen Anisimov, Andrey Alitalo, Kari De Palma, Michele Mazzone, Massimiliano EMBO Mol Med Research Articles Occlusion of the main arterial route redirects blood flow to the collateral circulation. We previously reported that macrophages genetically modified to express low levels of prolyl hydroxylase domain protein 2 (PHD2) display an arteriogenic phenotype, which promotes the formation of collateral vessels and protects the skeletal muscle from ischaemic necrosis. However, the molecular mechanisms underlying this process are unknown. Here, we demonstrate that femoral artery occlusion induces a switch in macrophage phenotype through angiopoietin-1 (ANG1)-mediated Phd2 repression. ANG blockade by a soluble trap prevented the downregulation of Phd2 expression in macrophages and their phenotypic switch, thus inhibiting collateral growth. ANG1-dependent Phd2 repression initiated a feed-forward loop mediated by the induction of the ANG receptor TIE2 in macrophages. Gene silencing and cell depletion strategies demonstrate that TIE2 induction in macrophages is required to promote their proarteriogenic functions, enabling collateral vessel formation following arterial obstruction. These results indicate an indispensable role for TIE2 in sustaining in situ programming of macrophages to a proarteriogenic, M2-like phenotype, suggesting possible new venues for the treatment of ischaemic disorders. WILEY-VCH Verlag 2013-06 2013-04-25 /pmc/articles/PMC3779447/ /pubmed/23616286 http://dx.doi.org/10.1002/emmm.201302695 Text en Copyright © 2013 The Authors. Published by John Wiley and Sons, Ltd on behalf of EMBO http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation. |
spellingShingle | Research Articles Hamm, Alexander Veschini, Lorenzo Takeda, Yukiji Costa, Sandra Delamarre, Estelle Squadrito, Mario Leonardo Henze, Anne-Theres Wenes, Mathias Serneels, Jens Pucci, Ferdinando Roncal, Carmen Anisimov, Andrey Alitalo, Kari De Palma, Michele Mazzone, Massimiliano PHD2 regulates arteriogenic macrophages through TIE2 signalling |
title | PHD2 regulates arteriogenic macrophages through TIE2 signalling |
title_full | PHD2 regulates arteriogenic macrophages through TIE2 signalling |
title_fullStr | PHD2 regulates arteriogenic macrophages through TIE2 signalling |
title_full_unstemmed | PHD2 regulates arteriogenic macrophages through TIE2 signalling |
title_short | PHD2 regulates arteriogenic macrophages through TIE2 signalling |
title_sort | phd2 regulates arteriogenic macrophages through tie2 signalling |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3779447/ https://www.ncbi.nlm.nih.gov/pubmed/23616286 http://dx.doi.org/10.1002/emmm.201302695 |
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