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Sökning: id:"swepub:oai:DiVA.org:oru-4621" > CD137 is expressed ...

CD137 is expressed in human atherosclerosis and promotes development of plaque inflammation in hypercholesterolemic mice

Olofsson, Peder S. (författare)
Karolinska Institutet
Söderström, Leif A. (författare)
Karolinska Institutet
Wågsäter, Dick (författare)
Karolinska Institutet,Örebro universitet,Hälsoakademin,University of Örebro, Sweden
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Sheikine, Yuri (författare)
Karolinska Institutet
Ocaya, Pauline (författare)
Örebro universitet,Institutionen för klinisk medicin,University of Örebro, Sweden
Lang, François (författare)
INSERM U601, Nantes, France
Rabu, Catherine (författare)
INSERM U601, Nantes, France
Chen, Lieping (författare)
Johns Hopkins University School of Medicine, Baltimore, USA
Rudling, Mats (författare)
Karolinska Institutet
Aukrust, Pål (författare)
University of Oslo, Norway
Hedin, Ulf (författare)
Karolinska Institutet
Paulsson-Berne, Gabrielle (författare)
Karolinska Institutet
Sirsjö, Allan (författare)
Örebro universitet,Hälsoakademin,University of Örebro, Sweden
Hansson, Göran K. (författare)
Karolinska Institutet
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 (creator_code:org_t)
Baltimore, Md. Lippincott Williams & Wilkins, 2008
2008
Engelska.
Ingår i: Circulation. - Baltimore, Md. : Lippincott Williams & Wilkins. - 0009-7322 .- 1524-4539. ; 117:10, s. 1292-1301
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Background— Atherosclerosis is a multifactorial disease in which inflammatory processes play an important role. Inflammation underlies lesion evolution at all stages, from establishment to plaque rupture and thrombosis. Costimulatory molecules of the tumor necrosis factor superfamily such as CD40/CD40L and OX40/OX40L have been implicated in atherosclerosis. Methods and Results— This study shows that the tumor necrosis factor superfamily members CD137 and CD137 ligand (CD137L), which play a major role in several autoimmune diseases, may constitute a pathogenic pair in atherogenesis. We detected CD137 protein in human atherosclerotic lesions not only on T cells but also on endothelial cells and showed that CD137 in cultured endothelial cells and smooth muscle cells was induced by proinflammatory cytokines implicated in atherosclerosis. Activation of CD137 by CD137L induced adhesion molecule expression on endothelial cells and reduced smooth muscle cell proliferation. In addition, treatment of atherosclerosis-prone apolipoprotein E–deficient mice with a CD137 agonist caused increased inflammation. T-cell infiltration, mainly of CD8+ cells, and expression of the murine major histocompatibility complex class II molecule I-Ab increased significantly in atherosclerotic lesions, as did the aortic expression of proinflammatory cytokines. Conclusions— Taken together, these observations suggest that CD137-CD137L interactions in the vasculature may contribute to the progression of atherosclerosis via augmented leukocyte recruitment, increased inflammation, and development of a more disease-prone phenotype.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kardiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cardiac and Cardiovascular Systems (hsv//eng)

Nyckelord

4-1BB Ligand/metabolism
Animals
Antigens; CD137/agonists/metabolism/*physiology
Apolipoproteins E/deficiency/genetics
Atherosclerosis/etiology/immunology/*metabolism
Carotid Arteries/cytology/physiology
Cells; Cultured
Histocompatibility Antigens Class II/metabolism
Humans
Hypercholesterolemia/complications/metabolism
Inflammation
Mice
Mice; Inbred C57BL
Mice; Knockout
RNA; Messenger/metabolism
Renal Artery/cytology/physiology
Statistics; Nonparametric
MEDICINE
MEDICIN
Cardiovascular medicine
Kardiovaskulär medicin
Medicine
Medicin

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