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Sökning: WFRF:(Zare A) > (2000-2004) > Arthritogenic prope...

Arthritogenic properties of double-stranded (viral) RNA

Zare, Fariba, 1972 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för invärtesmedicin, Avdelningen för reumatologi och inflammationsforskning,Institute of Internal Medicine, Dept of Rheumatology and Inflammation Research
Bokarewa, Maria, 1963 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för invärtesmedicin, Avdelningen för reumatologi och inflammationsforskning,Institute of Internal Medicine, Dept of Rheumatology and Inflammation Research
Nenonen, Nancy P, 1943 (författare)
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Bergström, Tomas, 1950 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för laboratoriemedicin, Avdelningen för klinisk virologi,Institute of Laboratory Medicine, Dept of Clinical Virology
Alexopoulou, L. (författare)
Flavell, R. A. (författare)
Tarkowski, Andrej, 1951 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för invärtesmedicin, Avdelningen för reumatologi och inflammationsforskning,Institute of Internal Medicine, Dept of Rheumatology and Inflammation Research
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 (creator_code:org_t)
2004
2004
Engelska.
Ingår i: J Immunol. - 0022-1767. ; 172:9, s. 5656-63
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Viral infections often lead to arthralgias and overt arthritic states. The inflammatogenic compound of the viruses giving rise to such an outcome has to date not been identified. Because expression of dsRNA is a common feature of all viruses, we decided to analyze whether this property leads to the induction of arthritis. Histological signs of arthritis were evident already on day 3 following intra-articular administration of dsRNA. Arthritis was characterized by infiltration of macrophages into synovial tissue. It was not dependent on acquired immune responses because SCID mice also raised joint inflammation. NF-kappa B was activated upon in vitro exposure to dsRNA, indicating its role in the induction/progression of arthritis. Importantly, we found that dsRNA arthritis was triggered through IL-1R signaling because mice being deficient for this molecule were unable to develop joint inflammation. Although dsRNA is typically recognized by Toll-like receptor 3, Toll-like receptor 3 knockout mice developed arthritis, indicating that some other receptors are instrumental in the inducing of inflammation. Our results from in vitro experiments indicate that proinflammatory cytokines and chemokines stimulating monocyte influx were readily triggered in response to stimulation with dsRNA. These findings demonstrate that viral dsRNA is clearly arthritogenic. Importantly, macrophages and their products play an important role in the development of arthritis triggered by dsRNA.

Nyckelord

Animals
Arthritis
Experimental/immunology/pathology/*virology
Cells
Cultured
Chemokines/biosynthesis
Cytokines/biosynthesis
Female
Injections
Intra-Articular
Interleukin-6/blood
Leukopenia/chemically induced/immunology
Macrophages/drug effects
Membrane Glycoproteins/physiology
Mice
Mice
Inbred BALB C
Mice
Inbred C3H
Mice
Inbred C57BL
Mice
Knockout
Mice
SCID
Monocytes/drug effects
NF-kappa B/physiology
Poly I-C/administration & dosage/toxicity
RNA
Double-Stranded/administration & dosage/chemical synthesis/*toxicity
RNA
Viral/administration & dosage/chemical synthesis/*toxicity
Receptors
Cell Surface/physiology
Rotavirus/chemistry
Toll-Like Receptor 3
Toll-Like Receptors

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