Literature DB >> 15037582

Susceptibility of retinal vascular endothelium to infection with Toxoplasma gondii tachyzoites.

Justine R Smith1, Daniel T Franc, Nicola S Carter, David Zamora, Stephen R Planck, James T Rosenbaum.   

Abstract

PURPOSE: Retinochoroidal infection with the protozoan parasite Toxoplasma gondii is the most common cause of posterior uveitis worldwide. Tachyzoites spread throughout the body through the blood stream and lymphatics, but preferentially encyst in the eye and other parts of the central nervous system (CNS). It is unknown whether T. gondii penetrates the CNS selectively or whether these sites of immune privilege have limited capacity to eradicate the parasite.
METHODS: Human vascular endothelial cell lines, including retinal (three lines from three different donors), aortic, umbilical vein, and dermal microvascular endothelium, as well as human foreskin fibroblasts, were grown to confluence in 24-well plates. Cells were incubated with RH-strain T. gondii tachyzoites in the presence of [(3)H]-uracil. Trichloroacetic acid-insoluble radioactivity was measured as an index of T. gondii proliferation, because tachyzoites, but not human cells, incorporate uracil directly through pyrimidine salvage.
RESULTS: Tachyzoites showed higher [(3)H]-uracil incorporation after incubation with retinal vascular endothelial cells in comparison with aortic (55% more), umbilical vein (33% more) and dermal (34% more) endothelial cells. In eight separate assays, significantly greater radioactivity was measured for tachyzoites cultured with retinal versus other cell subtypes (P < 0.05), except for one assay in which differences reached only borderline significance (P <or= 0.07). In contrast, experiments comparing different retinal endothelial lines revealed no difference between any pair. Growth of the tachyzoites was approximately 2.8-fold higher in retinal endothelium than in foreskin fibroblasts, the cell subtype often used to investigate processes of T. gondii infection.
CONCLUSIONS: Enhanced susceptibility of retinal vascular endothelium to infection by T. gondii tachyzoites may explain, at least in part, preferential localization of T. gondii to the retina. Susceptibility may relate to preferential binding of tachyzoites to the retinal vascular endothelial surface, relative ease of penetration into the cell, rate of replication within the cell and/or cell response to infection.

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Year:  2004        PMID: 15037582     DOI: 10.1167/iovs.03-1105

Source DB:  PubMed          Journal:  Invest Ophthalmol Vis Sci        ISSN: 0146-0404            Impact factor:   4.799


  11 in total

Review 1.  Immunity and Toxoplasma retinochoroiditis.

Authors:  G R Wallace; M R Stanford
Journal:  Clin Exp Immunol       Date:  2008-06-28       Impact factor: 4.330

2.  Endothelial cell invasion by Toxoplasma gondii: differences between cell types and parasite strains.

Authors:  Irma Cañedo-Solares; Montserrat Calzada-Ruiz; Luz Belinda Ortiz-Alegría; Alda Rocío Ortiz-Muñiz; Dolores Correa
Journal:  Parasitol Res       Date:  2013-06-10       Impact factor: 2.289

Review 3.  The molecular biology and immune control of chronic Toxoplasma gondii infection.

Authors:  Xiao-Yu Zhao; Sarah E Ewald
Journal:  J Clin Invest       Date:  2020-07-01       Impact factor: 14.808

4.  Soluble ephrin-B2 mediates apoptosis in retinal neovascularization and in endothelial cells.

Authors:  Michael H Davies; David O Zamora; Justine R Smith; Michael R Powers
Journal:  Microvasc Res       Date:  2009-02-13       Impact factor: 3.514

Review 5.  Role of the retinal vascular endothelial cell in ocular disease.

Authors:  Arpita S Bharadwaj; Binoy Appukuttan; Phillip A Wilmarth; Yuzhen Pan; Andrew J Stempel; Timothy J Chipps; Eric E Benedetti; David O Zamora; Dongseok Choi; Larry L David; Justine R Smith
Journal:  Prog Retin Eye Res       Date:  2012-09-11       Impact factor: 21.198

6.  Toxoplasma Retinochoroiditis with Chorioretinal Neovascularization in a Young Patient.

Authors:  Nikhila S Khandwala; Robert A Hyde; Cagri G Besirli
Journal:  Case Rep Ophthalmol       Date:  2021-04-16

7.  Toxoplasma gondii migration within and infection of human retina.

Authors:  João M Furtado; Liam M Ashander; Kathleen Mohs; Timothy J Chipps; Binoy Appukuttan; Justine R Smith
Journal:  PLoS One       Date:  2013-02-21       Impact factor: 3.240

8.  VEGF Production Is Regulated by the AKT/ERK1/2 Signaling Pathway and Controls the Proliferation of Toxoplasma gondii in ARPE-19 Cells.

Authors:  Juan-Hua Quan; Hassan Ahmed Hassan Ahmed Ismail; Guang-Ho Cha; Young-Joon Jo; Fei Fei Gao; In-Wook Choi; Jia-Qi Chu; Jae-Min Yuk; Young-Ha Lee
Journal:  Front Cell Infect Microbiol       Date:  2020-04-28       Impact factor: 5.293

9.  Optical coherence tomography angiography findings in macular toxoplasma retinochoroiditis: A case report.

Authors:  Alejandro L Perez; Rosa A Lozada; Andres Emanuelli; Armando L Oliver
Journal:  Am J Ophthalmol Case Rep       Date:  2020-06-02

Review 10.  Clinical features and treatment of ocular toxoplasmosis.

Authors:  Young-Hoon Park; Ho-Woo Nam
Journal:  Korean J Parasitol       Date:  2013-08-30       Impact factor: 1.341

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