NCK-dependent pericyte migration promotes pathological neovascularization in ischemic retinopathy
Pericytes are perivascular cells that regulate blood vessel formation and function. Here Dubrac et al. show that pericyte recruitment contributes to pathological neovascularisation in a mouse model of ischemic retinopathy, and that this depends on the regulation of PDGF-B signaling by NCK adaptor pr...
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2018-08-01
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Series: | Nature Communications |
Online Access: | https://doi.org/10.1038/s41467-018-05926-7 |
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doaj-f212c5aa389b4f57a14e393ebd8caa172021-05-11T10:25:27ZengNature Publishing GroupNature Communications2041-17232018-08-019111510.1038/s41467-018-05926-7NCK-dependent pericyte migration promotes pathological neovascularization in ischemic retinopathyAlexandre Dubrac0Steffen E. Künzel1Sandrine H. Künzel2Jinyu Li3Rachana Radhamani Chandran4Kathleen Martin5Daniel M. Greif6Ralf H. Adams7Anne Eichmann8Department of Internal Medicine, Yale Cardiovascular Research Center, Yale University School of MedicineDepartment of Internal Medicine, Yale Cardiovascular Research Center, Yale University School of MedicineDepartment of Internal Medicine, Yale Cardiovascular Research Center, Yale University School of MedicineDepartment of Internal Medicine, Yale Cardiovascular Research Center, Yale University School of MedicineDepartment of Internal Medicine, Yale Cardiovascular Research Center, Yale University School of MedicineDepartment of Internal Medicine, Yale Cardiovascular Research Center, Yale University School of MedicineDepartment of Internal Medicine, Yale Cardiovascular Research Center, Yale University School of MedicineDepartment of Tissue Morphogenesis and University of Münster, Faculty of Medicine, Max Planck Institute for Molecular BiomedicineDepartment of Internal Medicine, Yale Cardiovascular Research Center, Yale University School of MedicinePericytes are perivascular cells that regulate blood vessel formation and function. Here Dubrac et al. show that pericyte recruitment contributes to pathological neovascularisation in a mouse model of ischemic retinopathy, and that this depends on the regulation of PDGF-B signaling by NCK adaptor proteins.https://doi.org/10.1038/s41467-018-05926-7 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Alexandre Dubrac Steffen E. Künzel Sandrine H. Künzel Jinyu Li Rachana Radhamani Chandran Kathleen Martin Daniel M. Greif Ralf H. Adams Anne Eichmann |
spellingShingle |
Alexandre Dubrac Steffen E. Künzel Sandrine H. Künzel Jinyu Li Rachana Radhamani Chandran Kathleen Martin Daniel M. Greif Ralf H. Adams Anne Eichmann NCK-dependent pericyte migration promotes pathological neovascularization in ischemic retinopathy Nature Communications |
author_facet |
Alexandre Dubrac Steffen E. Künzel Sandrine H. Künzel Jinyu Li Rachana Radhamani Chandran Kathleen Martin Daniel M. Greif Ralf H. Adams Anne Eichmann |
author_sort |
Alexandre Dubrac |
title |
NCK-dependent pericyte migration promotes pathological neovascularization in ischemic retinopathy |
title_short |
NCK-dependent pericyte migration promotes pathological neovascularization in ischemic retinopathy |
title_full |
NCK-dependent pericyte migration promotes pathological neovascularization in ischemic retinopathy |
title_fullStr |
NCK-dependent pericyte migration promotes pathological neovascularization in ischemic retinopathy |
title_full_unstemmed |
NCK-dependent pericyte migration promotes pathological neovascularization in ischemic retinopathy |
title_sort |
nck-dependent pericyte migration promotes pathological neovascularization in ischemic retinopathy |
publisher |
Nature Publishing Group |
series |
Nature Communications |
issn |
2041-1723 |
publishDate |
2018-08-01 |
description |
Pericytes are perivascular cells that regulate blood vessel formation and function. Here Dubrac et al. show that pericyte recruitment contributes to pathological neovascularisation in a mouse model of ischemic retinopathy, and that this depends on the regulation of PDGF-B signaling by NCK adaptor proteins. |
url |
https://doi.org/10.1038/s41467-018-05926-7 |
work_keys_str_mv |
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