Lipocalin 2 deficiency impacts angiogenesis after ischemia in vivo and in vitro

Therapeutic neovascularization is a promising therapy option for patients with peripheral arterial disease. We followed in time the gene expression after induction of hind limb ischemia in mice with different patterns of blood flow restoration and identified lipocalin 2 (LCN2) as a strongly upregula...

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Main Authors: L Zhang, Z Aref, H A B Peters, M R de Vries, A Y Nossent, P H A Quax
Format: Article
Language:English
Published: Bioscientifica 2025-05-01
Series:Vascular Biology
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Online Access:https://vb.bioscientifica.com/view/journals/vb/7/1/VB-25-0001.xml
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author L Zhang
Z Aref
H A B Peters
M R de Vries
A Y Nossent
P H A Quax
author_facet L Zhang
Z Aref
H A B Peters
M R de Vries
A Y Nossent
P H A Quax
author_sort L Zhang
collection DOAJ
description Therapeutic neovascularization is a promising therapy option for patients with peripheral arterial disease. We followed in time the gene expression after induction of hind limb ischemia in mice with different patterns of blood flow restoration and identified lipocalin 2 (LCN2) as a strongly upregulated factor whose role in neovascularization deserves further investigation. In this study, we investigated the role of LCN2 in angiogenesis using the hind limb ischemia (HLI) model, ex vivo angiogenic aortic ring assay, and by assessing the pre-existing collaterals in the pial circulation in both Lcn2−/− mice and wild-type (WT) mice. This demonstrated an upregulated mRNA expression of Lcn2 after HLI and reduced post-ischemic angiogenesis in Lcn2−/− compared to WT mice. In the aortic ring assay, angiogenic sprouting was decreased in Lcn2−/− compared to WT mice. The blood flow recovery and arteriogenesis after HLI and preexisting collateral density in the pial circulation were similar in Lcn2−/− and WT mice. In vitro, siRNA-mediated LCN2 knockdown impaired HMVEC migration and tube formation. These results show that LCN2 is a potential pro-angiogenic factor and that LCN2 downregulation has a negative effect on angiogenesis in vivo and in vitro.
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series Vascular Biology
spelling doaj-art-fcc43dcb016e47268c34b1b51df6be8d2025-08-20T03:21:51ZengBioscientificaVascular Biology2516-56582025-05-017110.1530/VB-25-00011Lipocalin 2 deficiency impacts angiogenesis after ischemia in vivo and in vitroL Zhang0Z Aref1H A B Peters2M R de Vries3A Y Nossent4P H A Quax5Einthoven Laboratory for Experimental Vascular Medicine and Regenerative Medicine, Leiden University Medical Center, Leiden, The NetherlandsEinthoven Laboratory for Experimental Vascular Medicine and Regenerative Medicine, Leiden University Medical Center, Leiden, The NetherlandsEinthoven Laboratory for Experimental Vascular Medicine and Regenerative Medicine, Leiden University Medical Center, Leiden, The NetherlandsEinthoven Laboratory for Experimental Vascular Medicine and Regenerative Medicine, Leiden University Medical Center, Leiden, The NetherlandsDepartment of Nutrition, Exercise and Sports, University of Copenhagen, Copenhagen, DenmarkEinthoven Laboratory for Experimental Vascular Medicine and Regenerative Medicine, Leiden University Medical Center, Leiden, The NetherlandsTherapeutic neovascularization is a promising therapy option for patients with peripheral arterial disease. We followed in time the gene expression after induction of hind limb ischemia in mice with different patterns of blood flow restoration and identified lipocalin 2 (LCN2) as a strongly upregulated factor whose role in neovascularization deserves further investigation. In this study, we investigated the role of LCN2 in angiogenesis using the hind limb ischemia (HLI) model, ex vivo angiogenic aortic ring assay, and by assessing the pre-existing collaterals in the pial circulation in both Lcn2−/− mice and wild-type (WT) mice. This demonstrated an upregulated mRNA expression of Lcn2 after HLI and reduced post-ischemic angiogenesis in Lcn2−/− compared to WT mice. In the aortic ring assay, angiogenic sprouting was decreased in Lcn2−/− compared to WT mice. The blood flow recovery and arteriogenesis after HLI and preexisting collateral density in the pial circulation were similar in Lcn2−/− and WT mice. In vitro, siRNA-mediated LCN2 knockdown impaired HMVEC migration and tube formation. These results show that LCN2 is a potential pro-angiogenic factor and that LCN2 downregulation has a negative effect on angiogenesis in vivo and in vitro.https://vb.bioscientifica.com/view/journals/vb/7/1/VB-25-0001.xmllipocalin 2lcn2angiogenesisperipheral arterial diseaseendothelial cellmicrovasculature
spellingShingle L Zhang
Z Aref
H A B Peters
M R de Vries
A Y Nossent
P H A Quax
Lipocalin 2 deficiency impacts angiogenesis after ischemia in vivo and in vitro
Vascular Biology
lipocalin 2
lcn2
angiogenesis
peripheral arterial disease
endothelial cell
microvasculature
title Lipocalin 2 deficiency impacts angiogenesis after ischemia in vivo and in vitro
title_full Lipocalin 2 deficiency impacts angiogenesis after ischemia in vivo and in vitro
title_fullStr Lipocalin 2 deficiency impacts angiogenesis after ischemia in vivo and in vitro
title_full_unstemmed Lipocalin 2 deficiency impacts angiogenesis after ischemia in vivo and in vitro
title_short Lipocalin 2 deficiency impacts angiogenesis after ischemia in vivo and in vitro
title_sort lipocalin 2 deficiency impacts angiogenesis after ischemia in vivo and in vitro
topic lipocalin 2
lcn2
angiogenesis
peripheral arterial disease
endothelial cell
microvasculature
url https://vb.bioscientifica.com/view/journals/vb/7/1/VB-25-0001.xml
work_keys_str_mv AT lzhang lipocalin2deficiencyimpactsangiogenesisafterischemiainvivoandinvitro
AT zaref lipocalin2deficiencyimpactsangiogenesisafterischemiainvivoandinvitro
AT habpeters lipocalin2deficiencyimpactsangiogenesisafterischemiainvivoandinvitro
AT mrdevries lipocalin2deficiencyimpactsangiogenesisafterischemiainvivoandinvitro
AT aynossent lipocalin2deficiencyimpactsangiogenesisafterischemiainvivoandinvitro
AT phaquax lipocalin2deficiencyimpactsangiogenesisafterischemiainvivoandinvitro