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PMID: 11970999 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Quantitative expression of toll-like receptor 1-10 mRNA in cellular subsets of human peripheral blood mononuclear cells and sensitivity to CpG oligodeoxynucleotides.

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 168 ·No. 9 ·2002-05-01 ·Pages 4531-7

Hornung V, Rothenfusser S, Britsch S, Krug A, Jahrsdörfer B, Giese T, Endres S, Hartmann G

Abstract

The Toll-like receptor (TLR)9 is critical for the recognition of immunostimulatory CpG motifs but may cooperate with other TLRs. We analyzed TLR1-10 mRNA expression by using quantitative real-time PCR in highly purified subsets of human PBMC and determined the sensitivity of these subsets to CpG oligodeoxynucleotides (ODN). TLR1 and TLR6 were expressed in all cell types examined. TLR10 was highly expressed in B cells and weakly expressed in plasmacytoid dendritic cells (PDC). High expression of TLR2 was characteristic for monocytes. PDC and B cells expressed marked levels of TLR7 and TLR9 and were directly sensitive to CpG ODN. In CpG ODN-stimulated PDC and B cells, TLR9 expression rapidly decreased, as opposed to TLR7, which was up-regulated in PDC and decreased in B cells. In monocytes, NK cells, and T cells, TLR7 was absent. Despite low expression of TLR9, monocytes, NK cells, and T cells did not respond to CpG ODN in the absence of PDC but were activated in the presence of PDC. In conclusion, our studies provide evidence that PDC and B cells, but not monocytes, NK cells, or T cells, are primary targets of CpG ODN in peripheral blood. The characteristic expression pattern of TLR1-10 in cellular subsets of human PBMC is consistent with the concept that TLR9 is essential in the recognition of CpG ODN in PDC and B cells. In addition, selective regulation of TLR7 expression in PDC and B cells by CpG ODN revealed TLR7 as a candidate TLR potentially involved in modulating the recognition of CpG motifs.

MeSH Terms
Adjuvants, Immunologic/pharmacology B-Lymphocytes/drug effects,immunology Blood/immunology Cells, Cultured Clone Cells DNA-Binding Proteins/biosynthesis,genetics Dendritic Cells/drug effects,immunology Drosophila Proteins Gene Expression Regulation Humans Immunologic Memory Killer Cells, Natural/drug effects,immunology Kinetics Leukocytes, Mononuclear/classification,drug effects,immunology Membrane Glycoproteins/biosynthesis,genetics Monocytes/drug effects,immunology Oligodeoxyribonucleotides/pharmacology Polymerase Chain Reaction Protein Isoforms/biosynthesis,genetics RNA, Messenger/biosynthesis Receptors, Cell Surface/biosynthesis,genetics T-Lymphocytes/drug effects,immunology Toll-Like Receptor 1 Toll-Like Receptor 10 Toll-Like Receptor 2 Toll-Like Receptor 7 Toll-Like Receptor 9 Toll-Like Receptors
Chemicals
Adjuvants, Immunologic CPG-oligonucleotide DNA-Binding Proteins Drosophila Proteins Membrane Glycoproteins Oligodeoxyribonucleotides Protein Isoforms RNA, Messenger Receptors, Cell Surface TLR2 protein, human TLR7 protein, human TLR9 protein, human Toll-Like Receptor 1 Toll-Like Receptor 10 Toll-Like Receptor 2 Toll-Like Receptor 7 Toll-Like Receptor 9 Toll-Like Receptors
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Hornung Veit
Department of Internal Medicine, Division of Clinical Pharmacology, University of Munich, Munich, Germany.
Rothenfusser Simon
Britsch Stefanie
Krug Anne
Jahrsdörfer Bernd
Giese Thomas
Endres Stefan
Hartmann Gunther
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
2002-05-01
Pages
4531-7
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
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