Targeting LOXL2 for cardiac interstitial fibrosis and heart failure treatment
Lysyl oxidase-like 2 (LOXL2) is an enzyme that promotes scaffolding of extracellular matrix proteins. Here the authors show that LOXL2 is crucial for pressure-overload induced cardiac fibrosis, and that antibody-mediated inhibition or genetic disruption ofLoxl2in mice shows therapeutic potential for...
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Nature Portfolio
2016
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oai:doaj.org-article:3c49e4174d5d4829a56a0c196d697c782021-12-02T17:31:34ZTargeting LOXL2 for cardiac interstitial fibrosis and heart failure treatment10.1038/ncomms137102041-1723https://doaj.org/article/3c49e4174d5d4829a56a0c196d697c782016-12-01T00:00:00Zhttps://doi.org/10.1038/ncomms13710https://doaj.org/toc/2041-1723Lysyl oxidase-like 2 (LOXL2) is an enzyme that promotes scaffolding of extracellular matrix proteins. Here the authors show that LOXL2 is crucial for pressure-overload induced cardiac fibrosis, and that antibody-mediated inhibition or genetic disruption ofLoxl2in mice shows therapeutic potential for treatment of cardiac fibrosis.Jin YangKonstantinos SavvatisJong Seok KangPeidong FanHongyan ZhongKaren SchwartzVivian BarryAmanda Mikels-VigdalSerge KarpinskiDmytro KornyeyevJoanne AdamkewiczXuhui FengQiong ZhouChing ShangPraveen KumarDillon PhanMario KasnerBegoña LópezJavier DiezKeith C. WrightRoxanne L. KovacsPeng-Sheng ChenThomas QuertermousVictoria SmithLina YaoCarsten TschöpeChing-Pin ChangNature PortfolioarticleScienceQENNature Communications, Vol 7, Iss 1, Pp 1-15 (2016) |
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Science Q Jin Yang Konstantinos Savvatis Jong Seok Kang Peidong Fan Hongyan Zhong Karen Schwartz Vivian Barry Amanda Mikels-Vigdal Serge Karpinski Dmytro Kornyeyev Joanne Adamkewicz Xuhui Feng Qiong Zhou Ching Shang Praveen Kumar Dillon Phan Mario Kasner Begoña López Javier Diez Keith C. Wright Roxanne L. Kovacs Peng-Sheng Chen Thomas Quertermous Victoria Smith Lina Yao Carsten Tschöpe Ching-Pin Chang Targeting LOXL2 for cardiac interstitial fibrosis and heart failure treatment |
description |
Lysyl oxidase-like 2 (LOXL2) is an enzyme that promotes scaffolding of extracellular matrix proteins. Here the authors show that LOXL2 is crucial for pressure-overload induced cardiac fibrosis, and that antibody-mediated inhibition or genetic disruption ofLoxl2in mice shows therapeutic potential for treatment of cardiac fibrosis. |
format |
article |
author |
Jin Yang Konstantinos Savvatis Jong Seok Kang Peidong Fan Hongyan Zhong Karen Schwartz Vivian Barry Amanda Mikels-Vigdal Serge Karpinski Dmytro Kornyeyev Joanne Adamkewicz Xuhui Feng Qiong Zhou Ching Shang Praveen Kumar Dillon Phan Mario Kasner Begoña López Javier Diez Keith C. Wright Roxanne L. Kovacs Peng-Sheng Chen Thomas Quertermous Victoria Smith Lina Yao Carsten Tschöpe Ching-Pin Chang |
author_facet |
Jin Yang Konstantinos Savvatis Jong Seok Kang Peidong Fan Hongyan Zhong Karen Schwartz Vivian Barry Amanda Mikels-Vigdal Serge Karpinski Dmytro Kornyeyev Joanne Adamkewicz Xuhui Feng Qiong Zhou Ching Shang Praveen Kumar Dillon Phan Mario Kasner Begoña López Javier Diez Keith C. Wright Roxanne L. Kovacs Peng-Sheng Chen Thomas Quertermous Victoria Smith Lina Yao Carsten Tschöpe Ching-Pin Chang |
author_sort |
Jin Yang |
title |
Targeting LOXL2 for cardiac interstitial fibrosis and heart failure treatment |
title_short |
Targeting LOXL2 for cardiac interstitial fibrosis and heart failure treatment |
title_full |
Targeting LOXL2 for cardiac interstitial fibrosis and heart failure treatment |
title_fullStr |
Targeting LOXL2 for cardiac interstitial fibrosis and heart failure treatment |
title_full_unstemmed |
Targeting LOXL2 for cardiac interstitial fibrosis and heart failure treatment |
title_sort |
targeting loxl2 for cardiac interstitial fibrosis and heart failure treatment |
publisher |
Nature Portfolio |
publishDate |
2016 |
url |
https://doaj.org/article/3c49e4174d5d4829a56a0c196d697c78 |
work_keys_str_mv |
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