LRP5 is required for vascular development in deeper layers of the retina.

The low-density lipoprotein receptor-related protein 5 (LRP5) plays an important role in the development of retinal vasculature. LRP5 loss-of-function mutations cause incomplete development of retinal vessel network in humans as well as in mice. To understand the underlying mechanism for how LRP5 mu...

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Main Authors: Chun-hong Xia, Zipora Yablonka-Reuveni, Xiaohua Gong
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2010-07-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2907392?pdf=render
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spelling doaj-9237ae14db17426a84d11aa66fc465932020-11-24T22:03:59ZengPublic Library of Science (PLoS)PLoS ONE1932-62032010-07-0157e1167610.1371/journal.pone.0011676LRP5 is required for vascular development in deeper layers of the retina.Chun-hong XiaZipora Yablonka-ReuveniXiaohua GongThe low-density lipoprotein receptor-related protein 5 (LRP5) plays an important role in the development of retinal vasculature. LRP5 loss-of-function mutations cause incomplete development of retinal vessel network in humans as well as in mice. To understand the underlying mechanism for how LRP5 mutations lead to retinal vascular abnormalities, we have determined the retinal cell types that express LRP5 and investigated specific molecular and cellular functions that may be regulated by LRP5 signaling in the retina.We characterized the development of retinal vasculature in LRP5 mutant mice using specific retinal cell makers and a GFP transgene expressed in retinal endothelial cells. Our data revealed that retinal vascular endothelial cells predominantly formed cell clusters in the inner-plexiform layer of LRP5 mutant retina rather than sprouting out or migrating into deeper layers to form normal vascular network in the retina. The IRES-beta-galactosidase (LacZ) report gene under the control of the endogenous LRP5 promoter was highly expressed in Müller cells and was also weakly detected in endothelial cells of the retinal surface vasculature. Moreover, the LRP5 mutant mice had a reduction of a Müller cell-specific glutamine transporter, Slc38a5, and showed a decrease in b-wave amplitude of electroretinogram.LRP5 is not only essential for vascular endothelial cells to sprout, migrate and/or anastomose in the deeper plexus during retinal vasculature development but is also important for the functions of Müller cells and retinal interneurons. Müller cells may utilize LRP5-mediated signaling pathway to regulate vascular development in deeper layers and to maintain the function of retinal interneurons.http://europepmc.org/articles/PMC2907392?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Chun-hong Xia
Zipora Yablonka-Reuveni
Xiaohua Gong
spellingShingle Chun-hong Xia
Zipora Yablonka-Reuveni
Xiaohua Gong
LRP5 is required for vascular development in deeper layers of the retina.
PLoS ONE
author_facet Chun-hong Xia
Zipora Yablonka-Reuveni
Xiaohua Gong
author_sort Chun-hong Xia
title LRP5 is required for vascular development in deeper layers of the retina.
title_short LRP5 is required for vascular development in deeper layers of the retina.
title_full LRP5 is required for vascular development in deeper layers of the retina.
title_fullStr LRP5 is required for vascular development in deeper layers of the retina.
title_full_unstemmed LRP5 is required for vascular development in deeper layers of the retina.
title_sort lrp5 is required for vascular development in deeper layers of the retina.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2010-07-01
description The low-density lipoprotein receptor-related protein 5 (LRP5) plays an important role in the development of retinal vasculature. LRP5 loss-of-function mutations cause incomplete development of retinal vessel network in humans as well as in mice. To understand the underlying mechanism for how LRP5 mutations lead to retinal vascular abnormalities, we have determined the retinal cell types that express LRP5 and investigated specific molecular and cellular functions that may be regulated by LRP5 signaling in the retina.We characterized the development of retinal vasculature in LRP5 mutant mice using specific retinal cell makers and a GFP transgene expressed in retinal endothelial cells. Our data revealed that retinal vascular endothelial cells predominantly formed cell clusters in the inner-plexiform layer of LRP5 mutant retina rather than sprouting out or migrating into deeper layers to form normal vascular network in the retina. The IRES-beta-galactosidase (LacZ) report gene under the control of the endogenous LRP5 promoter was highly expressed in Müller cells and was also weakly detected in endothelial cells of the retinal surface vasculature. Moreover, the LRP5 mutant mice had a reduction of a Müller cell-specific glutamine transporter, Slc38a5, and showed a decrease in b-wave amplitude of electroretinogram.LRP5 is not only essential for vascular endothelial cells to sprout, migrate and/or anastomose in the deeper plexus during retinal vasculature development but is also important for the functions of Müller cells and retinal interneurons. Müller cells may utilize LRP5-mediated signaling pathway to regulate vascular development in deeper layers and to maintain the function of retinal interneurons.
url http://europepmc.org/articles/PMC2907392?pdf=render
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AT ziporayablonkareuveni lrp5isrequiredforvasculardevelopmentindeeperlayersoftheretina
AT xiaohuagong lrp5isrequiredforvasculardevelopmentindeeperlayersoftheretina
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