Bacterial CpG-DNA and lipopolysaccharides activate Toll-like receptors at distinct cellular compartments

Recognition by innate immune cells of the pathogen associated molecular patterns (PAMP) lipopolysaccharide (LPS) from Gram-negative bacteria and bacterial CpG-DNA depends on Toll-like receptor4 (TLR4) and TLR9, respectively. To define differences in the response to these distinct PAMP we compared a...

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Bibliographic Details
Published in:European journal of immunology, Vol. 32, No. 7 (2002), p. 1958-68
Main Author: Ahmad-Nejad, Parviz (Author)
Other Involved Persons: Häcker, Hans ; Rutz, Mark ; Bauer, Stefan ; Vabulas, Ramunas M ; Wagner, Hermann
Format: Article
Language:English
ISSN:1521-4141
Item Description:Date Completed 13.08.2002
Date Revised 15.11.2006
published: Print
Citation Status MEDLINE
Copyright: From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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245 1 0 |a Bacterial CpG-DNA and lipopolysaccharides activate Toll-like receptors at distinct cellular compartments 
500 |a Date Completed 13.08.2002 
500 |a Date Revised 15.11.2006 
500 |a published: Print 
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520 |a Recognition by innate immune cells of the pathogen associated molecular patterns (PAMP) lipopolysaccharide (LPS) from Gram-negative bacteria and bacterial CpG-DNA depends on Toll-like receptor4 (TLR4) and TLR9, respectively. To define differences in the response to these distinct PAMP we compared a key intracellular event, namely recruitment of myeloid differentiation marker 88 (MyD88) to the respective PAMP-initiated TLR signaling. Using MyD88-GFP fusion protein expressing macrophages we demonstrate that LPS and CpG-DNA trigger signaling from two different cellular locations: theformer at the cell membrane and the latter at the lysosomal compartment. While LPS does not require endocytosis to functionally associate with the membrane expressed TLR4/MD2 complex, internalization and endosomal maturation is conditional for CpG-DNA to activate TLR9. In support of these data TLR9 is not localized at the cell surface, but intracellularily. These data stress the need to characterize individual TLR at the very beginning of signal initiation in order to understand their diverse biological functions 
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653 2 |a Humans  |6 D006801 
653 2 |a Lipopolysaccharides  |6 D008070  |a *pharmacology  |6 Q000494 
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653 2 |a Membrane Glycoproteins  |6 D008562  |a *metabolism  |6 Q000378 
653 2 |a Mice  |6 D051379 
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653 2 |a Oligodeoxyribonucleotides  |6 D009838  |a *pharmacology  |6 Q000494 
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653 2 |a Signal Transduction  |6 D015398 
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655 7 |a Drosophila Proteins  |2 gnd 
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655 7 |a Toll-Like Receptor 9  |2 gnd 
655 7 |a Toll-Like Receptors  |2 gnd 
689 0 0 |A f  |a Journal Article 
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689 2 5 |a DNA-Binding Proteins 
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689 2 7 |a Lipopolysaccharides 
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700 1 |a Rutz, Mark  |e verfasserin  |4 aut 
700 1 |a Bauer, Stefan  |e verfasserin  |4 aut 
700 1 |a Vabulas, Ramunas M  |e verfasserin  |4 aut 
700 1 |a Wagner, Hermann  |e verfasserin  |4 aut 
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