Show simple item record

dc.contributor.authorNear, Richard I.en_US
dc.contributor.authorSmith, Richard S.en_US
dc.contributor.authorToselli, Paul A.en_US
dc.contributor.authorFreddo, Thomas F.en_US
dc.contributor.authorBloom, Alexander B.en_US
dc.contributor.authorVanden Borre, Pierreen_US
dc.contributor.authorSeldin, David C.en_US
dc.contributor.authorLerner, Adamen_US
dc.date.accessioned2012-01-11T21:40:12Z
dc.date.available2012-01-11T21:40:12Z
dc.date.copyright2009en_US
dc.date.issued2009-4-03en_US
dc.identifier.citationNear, Richard I., Richard S. Smith, Paul A. Toselli, Thomas F. Freddo, Alexander B. Bloom, Pierre Vanden Borre, David C. Seldin, Adam Lerner. "Loss of AND-34/BCAR3 expression in mice results in rupture of the adult lens" Molecular Vision 15:685-699. (2009)en_US
dc.identifier.issn1090-0535en_US
dc.identifier.urihttp://hdl.handle.net/2144/3224
dc.description.abstractPURPOSE. AND-34/BCAR3 (Breast Cancer Anti-Estrogen Resistance 3) associates with the focal adhesion adaptor protein, p130CAS/BCAR1. Expression of AND-34 regulates epithelial cell growth pattern, motility, and growth factor dependence. We sought to establish the effects of the loss of AND-34 expression in a mammalian organism. METHODS. AND-34−/− mice were generated by homologous recombination. Histopathology, in situ hybridization, and western blotting were performed on murine tissues. RESULTS. Western analyses confirmed total loss of expression in AND-34−/− splenic lymphocytes. Mice lacking AND-34 are fertile and have normal longevity. While AND-34 is widely expressed in wild type mice, histologic analysis of multiple organs in AND-34−/− mice is unremarkable and analyses of lymphocyte development show no overt changes. A small percentage of AND-34−/− mice show distinctive small white eye lesions resulting from the migration of ruptured cortical lens tissue into the anterior chamber. Following initial vacuolization and liquefaction of the lens cortex first observed at postnatal day three, posterior lens rupture occurs in all AND-34−/− mice, beginning as early as three weeks and seen in all mice at three months. Western blot analysis and in situ hybridization confirmed the presence of AND-34 RNA and protein in lens epithelial cells, particularly at the lens equator. Prior data link AND-34 expression to the activation of Akt signaling. While Akt Ser 473 phosphorylation was readily detectable in AND-34+/+ lens epithelial cells, it was markedly reduced in the AND-34−/− lens epithelium. Basal levels of p130Cas phosphorylation were higher in AND-34+/+ than in AND-34−/− lens epithelium. CONCLUSIONS. These results demonstrate the loss of AND-34 dysregulates focal adhesion complex signaling in lens epithelial cells and suggest that AND-34-mediated signaling is required for maintenance of the structural integrity of the adult ocular lens.en_US
dc.description.sponsorshipNational Institutes of Health (RO1 CA114094); Logica Foundationen_US
dc.language.isoenen_US
dc.publisherMolecular Visionen_US
dc.rightsThis is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.en_US
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/en_US
dc.titleLoss of AND-34/BCAR3 Expression in Mice Results in Rupture of the Adult Lensen_US
dc.typearticleen_US
dc.identifier.pubmedid19365570en_US
dc.identifier.pmcid2666772en_US


Files in this item

This item appears in the following Collection(s)

Show simple item record

This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Except where otherwise noted, this item's license is described as This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.