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Human Molecular Genetics Advance Access originally published online on February 9, 2008
Human Molecular Genetics 2008 17(11):1605-1612; doi:10.1093/hmg/ddn047
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© The Author 2008. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

A model for familial exudative vitreoretinopathy caused by LPR5 mutations

Chun-Hong Xia1, Haiquan Liu1, Debra Cheung1, Meng Wang1, Catherine Cheng2, Xin Du3, Bo Chang4, Bruce Beutler3 and Xiaohua Gong1,2,*

1 School of Optometry and Vision Science Program 2 UC Berkeley/UCSF Joint Bioengineering Graduate Program, University of California, Berkeley, Berkeley, CA 94720-2020, USA 3 Department of Genetics, The Scripps Research Institute, La Jolla, CA 92037, USA 4 The Jackson Laboratory, Bar Harbor, ME 04609, USA

* To whom correspondence should be addressed at: School of Optometry and Vision Science Program, University of California, Berkeley, 695 Minor Hall, Berkeley, CA 94720-2020, USA. Tel: +1 5106422491; Fax: +1 5106425086; Email: xgong{at}berkeley.edu

Received January 7, 2008; Revised February 1, 2008; Accepted February 7, 2008

We have identified a mouse recessive mutation that leads to attenuated and hyperpermeable retinal vessels, recapitulating some pathological features of familial exudative vitreoretinopathy (FEVR) in human patients. DNA sequencing reveals a single nucleotide insertion in the gene encoding the low-density lipoprotein receptor-related protein 5 (LRP5), causing a frame shift and resulting in the replacement of the C-terminal 39 amino acid residues by 20 new amino acids. This change eliminates the last three PPP(S/T)P repeats in the LRP5 cytoplasmic domain that are important for mediating Wnt/β-catenin signaling. Thus, mutant LRP5 protein is probably unable to mediate its downstream signaling. Immunostaining and three-dimensional reconstructions of retinal vasculature confirm attenuated retinal vessels. Ultrastructural data further reveal that some capillaries lack lumen structure in the mutant retina. We have also verified that LRP5 null mice develop similar alterations in the retinal vasculature. This study provides direct evidence that LRP5 is essential for the development of retinal vasculature, and suggests a novel role played by LRP5 in capillary maturation. LRP5 mutant mice can be a useful model to explore the clinical manifestations of FEVR.


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