Literature DB >> 18056381

Death receptor ligation or exposure to perforin trigger rapid egress of the intracellular parasite Toxoplasma gondii.

Emma K Persson1, Abela Mpobela Agnarson, Henrik Lambert, Niclas Hitziger, Hideo Yagita, Benedict J Chambers, Antonio Barragan, Alf Grandien.   

Abstract

The obligate intracellular parasite Toxoplasma gondii chronically infects up to one-third of the global population, can result in severe disease in immunocompromised individuals, and can be teratogenic. In this study, we demonstrate that death receptor ligation in T. gondii-infected cells leads to rapid egress of infectious parasites and lytic necrosis of the host cell, an active process mediated through the release of intracellular calcium as a consequence of caspase activation early in the apoptotic cascade. Upon acting on infected cells via death receptor- or perforin-dependent pathways, T cells induce rapid egress of infectious parasites able to infect surrounding cells, including the Ag-specific effector cells.

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Year:  2007        PMID: 18056381     DOI: 10.4049/jimmunol.179.12.8357

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  35 in total

1.  Transmission of Toxoplasma gondii from infected dendritic cells to natural killer cells.

Authors:  Catrine M Persson; Henrik Lambert; Polya P Vutova; Isabel Dellacasa-Lindberg; Joanna Nederby; Hideo Yagita; Hans-Gustaf Ljunggren; Alf Grandien; Antonio Barragan; Benedict J Chambers
Journal:  Infect Immun       Date:  2009-01-12       Impact factor: 3.441

2.  Cell death of gamma interferon-stimulated human fibroblasts upon Toxoplasma gondii infection induces early parasite egress and limits parasite replication.

Authors:  Wendy Niedelman; Joris K Sprokholt; Barbara Clough; Eva-Maria Frickel; Jeroen P J Saeij
Journal:  Infect Immun       Date:  2013-09-16       Impact factor: 3.441

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.  Externally triggered egress is the major fate of Toxoplasma gondii during acute infection.

Authors:  Tadakimi Tomita; Tatsuya Yamada; Louis M Weiss; Amos Orlofsky
Journal:  J Immunol       Date:  2009-10-21       Impact factor: 5.422

5.  CD40 in Endothelial Cells Restricts Neural Tissue Invasion by Toxoplasma gondii.

Authors:  Jose-Andres C Portillo; Jennifer Van Grol; Saad Saffo; Yalitza Lopez Corcino; Myriam Rodriguez; Barbara A Fox; David J Bzik; Nicole L Ward; George R Dubyak; Roxana E Rojas; Zahra Toosi; Carlos S Subauste
Journal:  Infect Immun       Date:  2019-07-23       Impact factor: 3.441

Review 6.  Prison break: pathogens' strategies to egress from host cells.

Authors:  Nikolas Friedrich; Monica Hagedorn; Dominique Soldati-Favre; Thierry Soldati
Journal:  Microbiol Mol Biol Rev       Date:  2012-12       Impact factor: 11.056

7.  Impact of Toxoplasma gondii on Dendritic Cell Subset Function in the Intestinal Mucosa.

Authors:  Sara B Cohen; Eric Y Denkers
Journal:  J Immunol       Date:  2015-08-17       Impact factor: 5.422

8.  The P-glycoprotein inhibitor GF120918 modulates Ca2+-dependent processes and lipid metabolism in Toxoplasma gondii.

Authors:  Iveta Bottova; Ursula Sauder; Vesna Olivieri; Adrian B Hehl; Sabrina Sonda
Journal:  PLoS One       Date:  2010-04-08       Impact factor: 3.240

9.  Disruption of the Toxoplasma gondii parasitophorous vacuole by IFNgamma-inducible immunity-related GTPases (IRG proteins) triggers necrotic cell death.

Authors:  Yang O Zhao; Aliaksandr Khaminets; Julia P Hunn; Jonathan C Howard
Journal:  PLoS Pathog       Date:  2009-02-06       Impact factor: 6.823

10.  Toxoplasma gondii infection specifically increases the levels of key host microRNAs.

Authors:  Gusti M Zeiner; Kara L Norman; J Michael Thomson; Scott M Hammond; John C Boothroyd
Journal:  PLoS One       Date:  2010-01-15       Impact factor: 3.240

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