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AKAP12 regulates human blood-retinal barrier formation by downregulation of hypoxia-inducible factor-1alpha

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Authors
Choi, Yoon Kyung; Kim, Jeong Hun; Kim, Woo Jean; Lee, Hae Young; Park, Jeong Ae; Lee, Sae-Won; Yoon, Dae-Kwan; Kim, Hyun Ho; Chung, Hum; Yu, Young Suk; Kim, Kyu-Won
Issue Date
2007-04-20
Publisher
Society for Neuroscience
Citation
J Neurosci. 2007 Apr 18;27(16):4472-81.
Keywords
A Kinase Anchor ProteinsAngiopoietin-1/metabolismBlood-Retinal Barrier/embryology/*physiologyCell Cycle Proteins/*physiologyCells, CulturedDown-RegulationHumansHypoxia-Inducible Factor 1, alpha Subunit/*metabolismRetinal Neoplasms/metabolismRetinoblastoma/metabolismTight Junctions/*metabolismVascular Endothelial Growth Factor A/metabolism
Abstract
Many diseases of the eye such as retinoblastoma, diabetic retinopathy, and retinopathy of prematurity are associated with blood-retinal barrier (BRB) dysfunction. Identifying the factors that contribute to BRB formation during human eye development and maintenance could provide insights into such diseases. Here we show that A-kinase anchor protein 12 (AKAP12) induces BRB formation by increasing angiopoietin-1 and decreasing vascular endothelial growth factor (VEGF) levels in astrocytes. We reveal that AKAP12 downregulates the level of hypoxia-inducible factor-1alpha (HIF-1alpha) protein by enhancing the interaction of HIF-1alpha with pVHL (von Hippel-Lindau tumor suppressor protein) and PHD2 (prolyl hydroxylase 2). Conditioned media from AKAP12-overexpressing astrocytes induced barriergenesis by upregulating the expression of tight junction proteins in human retina microvascular endothelial cells (HRMECs). Compared with the retina during BRB maturation, AKAP12 expression in retinoblastoma patient tissue was markedly reduced whereas that of VEGF was increased. These findings suggest that AKAP12 may induce BRB formation through antiangiogenesis and barriergenesis in the developing human eye and that defects in this mechanism can lead to a loss of tight junction proteins and contribute to the development of retinal pathologies such as retinoblastoma.
ISSN
1529-2401 (Electronic)
Language
English
URI
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=17442832

http://hdl.handle.net/10371/18429
DOI
https://doi.org/10.1523/JNEUROSCI.5368-06.2007
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College of Medicine/School of Medicine (의과대학/대학원)Ophthalmology (안과학전공)Journal Papers (저널논문_안과학전공)
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