Publication Date:
2008-09-30
Description:
Mammalian Toll-like receptors (TLRs) 3, 7, 8 and 9 initiate immune responses to infection by recognizing microbial nucleic acids; however, these responses come at the cost of potential autoimmunity owing to inappropriate recognition of self nucleic acids. The localization of TLR9 and TLR7 to intracellular compartments seems to have a role in facilitating responses to viral nucleic acids while maintaining tolerance to self nucleic acids, yet the cell biology regulating the transport and localization of these receptors remains poorly understood. Here we define the route by which TLR9 and TLR7 exit the endoplasmic reticulum and travel to endolysosomes in mouse macrophages and dendritic cells. The ectodomains of TLR9 and TLR7 are cleaved in the endolysosome, such that no full-length protein is detectable in the compartment where ligand is recognized. Notably, although both the full-length and cleaved forms of TLR9 are capable of binding ligand, only the processed form recruits MyD88 on activation, indicating that this truncated receptor, rather than the full-length form, is functional. Furthermore, conditions that prevent receptor proteolysis, including forced TLR9 surface localization, render the receptor non-functional. We propose that ectodomain cleavage represents a strategy to restrict receptor activation to endolysosomal compartments and prevent TLRs from responding to self nucleic acids.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2596276/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉 〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2596276/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ewald, Sarah E -- Lee, Bettina L -- Lau, Laura -- Wickliffe, Katherine E -- Shi, Guo-Ping -- Chapman, Harold A -- Barton, Gregory M -- AI072429/AI/NIAID NIH HHS/ -- CA009179/CA/NCI NIH HHS/ -- HL67204/HL/NHLBI NIH HHS/ -- R01 AI072429/AI/NIAID NIH HHS/ -- R01 AI072429-01A2/AI/NIAID NIH HHS/ -- England -- Nature. 2008 Dec 4;456(7222):658-62. doi: 10.1038/nature07405. Epub 2008 Sep 28.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Division of Immunology & Pathogenesis, Department of Molecular and Cell Biology, University of California, Berkeley, 405 Life Sciences Addition, Berkeley, California 94720-3200, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18820679" target="_blank"〉PubMed〈/a〉
Keywords:
Animals
;
Cell Line
;
Cells, Cultured
;
Dendritic Cells/cytology/metabolism
;
Endoplasmic Reticulum/metabolism
;
Female
;
Golgi Apparatus/metabolism
;
Ligands
;
Lysosomes/metabolism
;
Macrophages/cytology/metabolism
;
Male
;
Membrane Glycoproteins/chemistry/metabolism
;
Membrane Transport Proteins/genetics/metabolism
;
Mice
;
Myeloid Differentiation Factor 88/metabolism
;
Phagosomes/metabolism
;
*Protein Processing, Post-Translational
;
Protein Structure, Tertiary
;
Protein Transport
;
Toll-Like Receptor 7/chemistry/metabolism
;
Toll-Like Receptor 9/*chemistry/*metabolism
Print ISSN:
0028-0836
Electronic ISSN:
1476-4687
Topics:
Biology
,
Chemistry and Pharmacology
,
Medicine
,
Natural Sciences in General
,
Physics
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