Disruption of profilin1 function suppresses developmental and pathological retinal neovascularization.

Profilin1 (PFN1) actin angiogenesis cytoskeleton diabetic retinopathy filopodia oxygen-induced retinopathy (OIR) profilin retina tip cells vascular endothelial cells (VECs) vascularization

Journal

The Journal of biological chemistry
ISSN: 1083-351X
Titre abrégé: J Biol Chem
Pays: United States
ID NLM: 2985121R

Informations de publication

Date de publication:
10 07 2020
Historique:
received: 10 01 2020
revised: 20 05 2020
pubmed: 24 5 2020
medline: 14 1 2021
entrez: 24 5 2020
Statut: ppublish

Résumé

Angiogenesis-mediated neovascularization in the eye is usually associated with visual complications. Pathological angiogenesis is particularly prominent in the retina in the settings of proliferative diabetic retinopathy, in which it can lead to permanent loss of vision. In this study, by bioinformatics analyses, we provide evidence for elevated expression of actin-binding protein PFN1 (profilin1) in the retinal vascular endothelial cells (VECs) of individuals with proliferative diabetic retinopathy, findings further supported by gene expression analyses for PFN1 in experimentally induced abnormal retinal neovascularization in an oxygen-induced retinopathy murine model. We observed that in a conditional knockout mouse model, postnatal deletion of the

Identifiants

pubmed: 32444495
pii: S0021-9258(17)48978-2
doi: 10.1074/jbc.RA120.012613
pmc: PMC7363146
doi:

Substances chimiques

Pfn1 protein, mouse 0
Profilins 0
Oxygen S88TT14065

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

9618-9629

Subventions

Organisme : NIH HHS
ID : S10 OD019973
Pays : United States
Organisme : NHLBI NIH HHS
ID : T32 HL129964
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM108340
Pays : United States
Organisme : NHLBI NIH HHS
ID : T32 HL076124
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA108607
Pays : United States

Informations de copyright

© 2020 Gau et al.

Déclaration de conflit d'intérêts

Conflict of interest—The authors declare that they have no conflicts of interest with the contents of this article.

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Auteurs

David Gau (D)

Department of Bioengineering, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.

Lucile Vignaud (L)

Institut de la Vision, Sorbonne Université, INSERM, Paris, France.

Abigail Allen (A)

Department of Bioengineering, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.

Zhijian Guo (Z)

Department of Nephrology, Southern Medical University, Guangzhou, China.

Jose Sahel (J)

Institut de la Vision, Sorbonne Université, INSERM, Paris, France.
Department of Ophthalmology, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.

David Boone (D)

Department of Biomedical Informatics, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.

David Koes (D)

Department of Computational Biology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.

Xavier Guillonneau (X)

Institut de la Vision, Sorbonne Université, INSERM, Paris, France xavier.guillonneau@inserm.fr par19@pitt.edu Partha.Roy@pitt.edu.

Partha Roy (P)

Department of Bioengineering, University of Pittsburgh, Pittsburgh, Pennsylvania, USA xavier.guillonneau@inserm.fr par19@pitt.edu Partha.Roy@pitt.edu.
Department of Pathology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.

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