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AuthorIbrahim, Ahmed S.
AuthorTawfik, Amany M.
AuthorHussein, Khaled A.
AuthorElshafey, Sally
AuthorMarkand, Shanu
AuthorRizk, Nasser
AuthorDuh, Elia J.
AuthorSmith, Sylvia B.
AuthorAl-Shabrawey, Mohamed
Available date2016-11-21T10:03:02Z
Publication Date2015-03
Publication NameBiochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids
Identifierhttp://dx.doi.org/10.1016/j.bbalip.2014.12.017
CitationAhmed S. Ibrahim, Amany M. Tawfik, Khaled A. Hussein, Sally Elshafey, Shanu Markand, Nasser Rizk, Elia J. Duh, Sylvia B. Smith, Mohamed Al-Shabrawey, Pigment epithelium-derived factor inhibits retinal microvascular dysfunction induced by 12/15-lipoxygenase-derived eicosanoids, Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids, Volume 1851, Issue 3, March 2015, Pages 290-298
ISSN13881981
URIhttp://www.sciencedirect.com/science/article/pii/S1388198114002765
URIhttp://hdl.handle.net/10576/5031
AbstractWe recently demonstrated that 12/15-lipoxygenase (LOX) derived metabolites, hydroxyeicosatetraenoic acids (HETEs), contribute to diabetic retinopathy (DR) via NADPH oxidase (NOX) and disruption of the balance in retinal levels of the vascular endothelial growth factor (VEGF) and pigment epithelium-derived factor (PEDF). Here, we test whether PEDF ameliorates retinal vascular injury induced by HETEs and the underlying mechanisms. Furthermore, we pursue the causal relationship between LOX–NOX system and regulation of PEDF expression during DR. For these purposes, we used an experimental eye model in which normal mice were injected intravitreally with 12-HETE with/without PEDF. Thereafter, fluorescein angiography (FA) was used to evaluate the vascular leakage, followed by optical coherence tomography (OCT) to assess the presence of angiogenesis. FA and OCT reported an increased vascular leakage and pre-retinal neovascularization, respectively, in response to 12-HETE that were not observed in the PEDF-treated group. Moreover, PEDF significantly attenuated the increased levels of vascular cell and intercellular adhesion molecules, VCAM-1 and ICAM-1, elicited by 12-HETE injection. Accordingly, the direct relationship between HETEs and PEDF has been explored through in-vitro studies using Müller cells (rMCs) and human retinal endothelial cells (HRECs). The results showed that 12- and 15-HETEs triggered the secretion of TNF-α and IL-6, as well as activation of NFκB in rMCs and significantly increased permeability and reduced zonula occludens protein-1 (ZO-1) immunoreactivity in HRECs. All these effects were prevented in PEDF-treated cells. Furthermore, interest in PEDF regulation during DR has been expanded to include NOX system. Retinal PEDF was significantly restored in diabetic mice treated with NOX inhibitor, apocynin, or lacking NOX2 up to 80% of the control level. Collectively, our findings suggest that interfering with LOX–NOX signaling opens up a new direction for treating DR by restoring endogenous PEDF that carries out multilevel vascular protective functions.
SponsorNational Eye Institute 5R01EY023315-02, Qatar National Research Fund NPRP 4-1046-3-284, and Vision Discovery Institute (MA), Mr. and Mrs. Richards travel award (ASI).
Languageen
PublisherElsevier
SubjectDiabetic retinopathy
PEDF
12/15-Lipoxygenase
12/15 HETEs
Retinal vascular leakage
Retinal inflammation
TitlePigment epithelium-derived factor inhibits retinal microvascular dysfunction induced by 12/15-lipoxygenase-derived eicosanoids
TypeArticle
Pagination290-298
Issue Number3
Volume Number1851
dc.accessType Open Access


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