Cargando…
Evolutionarily conserved recognition and innate immunity to fungal pathogens by the scavenger receptors SCARF1 and CD36
Receptors involved in innate immunity to fungal pathogens have not been fully elucidated. We show that the Caenorhabditis elegans receptors CED-1 and C03F11.3, and their mammalian orthologues, the scavenger receptors SCARF1 and CD36, mediate host defense against two prototypic fungal pathogens, Cryp...
Autores principales: | , , , , , , , , , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2009
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2699123/ https://www.ncbi.nlm.nih.gov/pubmed/19237602 http://dx.doi.org/10.1084/jem.20082109 |
_version_ | 1782168462919991296 |
---|---|
author | Means, Terry K. Mylonakis, Eleftherios Tampakakis, Emmanouil Colvin, Richard A. Seung, Edward Puckett, Lindsay Tai, Melissa F. Stewart, Cameron R. Pukkila-Worley, Read Hickman, Suzanne E. Moore, Kathryn J. Calderwood, Stephen B. Hacohen, Nir Luster, Andrew D. El Khoury, Joseph |
author_facet | Means, Terry K. Mylonakis, Eleftherios Tampakakis, Emmanouil Colvin, Richard A. Seung, Edward Puckett, Lindsay Tai, Melissa F. Stewart, Cameron R. Pukkila-Worley, Read Hickman, Suzanne E. Moore, Kathryn J. Calderwood, Stephen B. Hacohen, Nir Luster, Andrew D. El Khoury, Joseph |
author_sort | Means, Terry K. |
collection | PubMed |
description | Receptors involved in innate immunity to fungal pathogens have not been fully elucidated. We show that the Caenorhabditis elegans receptors CED-1 and C03F11.3, and their mammalian orthologues, the scavenger receptors SCARF1 and CD36, mediate host defense against two prototypic fungal pathogens, Cryptococcus neoformans and Candida albicans. CED-1 and C03F11.1 mediated antimicrobial peptide production and were necessary for nematode survival after C. neoformans infection. SCARF1 and CD36 mediated cytokine production and were required for macrophage binding to C. neoformans, and control of the infection in mice. Binding of these pathogens to SCARF1 and CD36 was β-glucan dependent. Thus, CED-1/SCARF1 and C03F11.3/CD36 are β-glucan binding receptors and define an evolutionarily conserved pathway for the innate sensing of fungal pathogens. |
format | Text |
id | pubmed-2699123 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-26991232009-09-16 Evolutionarily conserved recognition and innate immunity to fungal pathogens by the scavenger receptors SCARF1 and CD36 Means, Terry K. Mylonakis, Eleftherios Tampakakis, Emmanouil Colvin, Richard A. Seung, Edward Puckett, Lindsay Tai, Melissa F. Stewart, Cameron R. Pukkila-Worley, Read Hickman, Suzanne E. Moore, Kathryn J. Calderwood, Stephen B. Hacohen, Nir Luster, Andrew D. El Khoury, Joseph J Exp Med Article Receptors involved in innate immunity to fungal pathogens have not been fully elucidated. We show that the Caenorhabditis elegans receptors CED-1 and C03F11.3, and their mammalian orthologues, the scavenger receptors SCARF1 and CD36, mediate host defense against two prototypic fungal pathogens, Cryptococcus neoformans and Candida albicans. CED-1 and C03F11.1 mediated antimicrobial peptide production and were necessary for nematode survival after C. neoformans infection. SCARF1 and CD36 mediated cytokine production and were required for macrophage binding to C. neoformans, and control of the infection in mice. Binding of these pathogens to SCARF1 and CD36 was β-glucan dependent. Thus, CED-1/SCARF1 and C03F11.3/CD36 are β-glucan binding receptors and define an evolutionarily conserved pathway for the innate sensing of fungal pathogens. The Rockefeller University Press 2009-03-16 /pmc/articles/PMC2699123/ /pubmed/19237602 http://dx.doi.org/10.1084/jem.20082109 Text en © 2009 Means et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.jem.org/misc/terms.shtml). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Article Means, Terry K. Mylonakis, Eleftherios Tampakakis, Emmanouil Colvin, Richard A. Seung, Edward Puckett, Lindsay Tai, Melissa F. Stewart, Cameron R. Pukkila-Worley, Read Hickman, Suzanne E. Moore, Kathryn J. Calderwood, Stephen B. Hacohen, Nir Luster, Andrew D. El Khoury, Joseph Evolutionarily conserved recognition and innate immunity to fungal pathogens by the scavenger receptors SCARF1 and CD36 |
title | Evolutionarily conserved recognition and innate immunity to fungal pathogens by the scavenger receptors SCARF1 and CD36 |
title_full | Evolutionarily conserved recognition and innate immunity to fungal pathogens by the scavenger receptors SCARF1 and CD36 |
title_fullStr | Evolutionarily conserved recognition and innate immunity to fungal pathogens by the scavenger receptors SCARF1 and CD36 |
title_full_unstemmed | Evolutionarily conserved recognition and innate immunity to fungal pathogens by the scavenger receptors SCARF1 and CD36 |
title_short | Evolutionarily conserved recognition and innate immunity to fungal pathogens by the scavenger receptors SCARF1 and CD36 |
title_sort | evolutionarily conserved recognition and innate immunity to fungal pathogens by the scavenger receptors scarf1 and cd36 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2699123/ https://www.ncbi.nlm.nih.gov/pubmed/19237602 http://dx.doi.org/10.1084/jem.20082109 |
work_keys_str_mv | AT meansterryk evolutionarilyconservedrecognitionandinnateimmunitytofungalpathogensbythescavengerreceptorsscarf1andcd36 AT mylonakiseleftherios evolutionarilyconservedrecognitionandinnateimmunitytofungalpathogensbythescavengerreceptorsscarf1andcd36 AT tampakakisemmanouil evolutionarilyconservedrecognitionandinnateimmunitytofungalpathogensbythescavengerreceptorsscarf1andcd36 AT colvinricharda evolutionarilyconservedrecognitionandinnateimmunitytofungalpathogensbythescavengerreceptorsscarf1andcd36 AT seungedward evolutionarilyconservedrecognitionandinnateimmunitytofungalpathogensbythescavengerreceptorsscarf1andcd36 AT puckettlindsay evolutionarilyconservedrecognitionandinnateimmunitytofungalpathogensbythescavengerreceptorsscarf1andcd36 AT taimelissaf evolutionarilyconservedrecognitionandinnateimmunitytofungalpathogensbythescavengerreceptorsscarf1andcd36 AT stewartcameronr evolutionarilyconservedrecognitionandinnateimmunitytofungalpathogensbythescavengerreceptorsscarf1andcd36 AT pukkilaworleyread evolutionarilyconservedrecognitionandinnateimmunitytofungalpathogensbythescavengerreceptorsscarf1andcd36 AT hickmansuzannee evolutionarilyconservedrecognitionandinnateimmunitytofungalpathogensbythescavengerreceptorsscarf1andcd36 AT moorekathrynj evolutionarilyconservedrecognitionandinnateimmunitytofungalpathogensbythescavengerreceptorsscarf1andcd36 AT calderwoodstephenb evolutionarilyconservedrecognitionandinnateimmunitytofungalpathogensbythescavengerreceptorsscarf1andcd36 AT hacohennir evolutionarilyconservedrecognitionandinnateimmunitytofungalpathogensbythescavengerreceptorsscarf1andcd36 AT lusterandrewd evolutionarilyconservedrecognitionandinnateimmunitytofungalpathogensbythescavengerreceptorsscarf1andcd36 AT elkhouryjoseph evolutionarilyconservedrecognitionandinnateimmunitytofungalpathogensbythescavengerreceptorsscarf1andcd36 |