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Estrogen receptor beta protects against in vivo injury in RPE cells.

Authors: Elliot, SJ  Catanuto, P  Espinosa-Heidmann, DG  Fernandez, P  Hernandez, E  Saloupis, P  Korach, K  Karl, M  Cousins, SW 
Citation: Elliot SJ, etal., Exp Eye Res. 2010 Jan;90(1):10-6. doi: 10.1016/j.exer.2009.09.001. Epub 2009 Sep 30.
Pubmed: (View Article at PubMed) PMID:19799898
DOI: Full-text: DOI:10.1016/j.exer.2009.09.001

Epidemiological data suggest that estrogen deficiency in postmenopausal women may contribute to the severity of AMD. We discovered that 17beta-estradiol (E2) was a crucial regulator of the severity of extracellular matrix turnover (ECM) dysregulation both in vivo and in vitro. We also found in vitro that the presence of estrogen receptor (ER)beta regulates MMP-2 activity. Therefore in an attempt to delineate the role of the ER subtypes, female estrogen receptor knockout (ERKO) mice were fed a high-fat diet, and the eyes were exposed to seven 5-second doses of nonphototoxic levels of blue-green light over 2 weeks. Three months after cessation of blue light treatment, transmission electron microscopy was performed to assess severity of deposits, Bruchs membrane changes, and choriocapillaris endothelial morphology. We found that changes in the trimolecular complex of pro-MMP-2, MMP-14 and TIMP-2 correlated with increased Bruch's membrane thickening or sub-retinal deposit formation (basal laminar deposits) in ERKObeta mice. In addition RPE isolated from ERKObeta mice had an increase in expression of total collagen and a decrease in MMP-2 activity. Finally we found that ERK an intermediate signaling molecule in the MMP pathway was activated in RPE isolated from ERKObeta mice. These data suggest that mice which lack ERbeta are more susceptible to in vivo injury associated with environmental light and high fat diet.

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RGD ID: 8694106
Created: 2014-07-24
Species: All species
Last Modified: 2014-07-24
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.