Protease nexin-1 regulates retinal vascular development View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2015-06-25

AUTHORS

Sonia Selbonne, Deborah Francois, William Raoul, Yacine Boulaftali, Florian Sennlaub, Martine Jandrot-Perrus, Marie-Christine Bouton, Véronique Arocas

ABSTRACT

We recently identified protease nexin-1 (PN-1) or serpinE2, as a possibly underestimated player in maintaining angiogenic balance. Here, we used the well-characterized postnatal vascular development of newborn mouse retina to further investigate the role and the mechanism of action of PN-1 in physiological angiogenesis. The development of retinal vasculature was analysed by endothelial cell staining with isolectin B4. PN-1-deficient (PN-1−/−) retina displayed increased vascularization in the postnatal period, with elevated capillary thickness and density, compared to their wild-type littermate (WT). Moreover, PN-1−/− retina presented more veins/arteries than WT retina. The kinetics of retinal vasculature development, retinal VEGF expression and overall retinal structure were similar in WT and PN-1−/− mice, but we observed a hyperproliferation of vascular cells in PN-1−/− retina. Expression of PN-1 was analysed by immunoblotting and X-Gal staining of retinas from mice expressing beta-galactosidase under a PN-1 promoter. PN-1 was highly expressed in the first week following birth and then progressively decreased to a low level in adult retina where it localized on the retinal arteries. PCR arrays performed on mouse retinal RNA identified two angiogenesis-related factors, midkine and Smad5, that were overexpressed in PN-1−/− newborn mice and this was confirmed by RT-PCR. Both the higher vascularization and the overexpression of midkine and Smad5 mRNA were also observed in gastrocnemius muscle of PN-1−/− mice, suggesting that PN-1 interferes with these pathways. Together, our results demonstrate that PN-1 strongly limits physiological angiogenesis and suggest that modulation of PN-1 expression could represent a new way to regulate angiogenesis. More... »

PAGES

3999-4011

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s00018-015-1972-5

DOI

http://dx.doi.org/10.1007/s00018-015-1972-5

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1018233922

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/26109427


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