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The A2b adenosine receptor protects against inflammation and excessive vascular adhesion

Young, D. (author)
Boston University School of Medicine
Zhang, Y (author)
Boston University School of Medicine
Nguyen, H G (author)
Boston University School of Medicine
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Koupenova, M. (author)
Boston University School of Medicine
Chauhan, A K (author)
Boston University School of Medicine
Mäkitalo, Maria (author)
Jones, M R (author)
Boston University School of Medicine
Hilaire, C. St (author)
Boston University School of Medicine
Seldin, D C (author)
Boston University School of Medicine
Toselli, P (author)
Boston University School of Medicine
Lamperti, E (author)
Boston University School of Medicine
Schreiber, B M (author)
Boston University School of Medicine
Gavras, H (author)
Boston University School of Medicine
Wagner, D D (author)
Boston University School of Medicine
Ravid, K (author)
Boston University School of Medicine
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 (creator_code:org_t)
2006
2006
English.
In: Journal of Clinical Investigation. - 0021-9738 .- 1558-8238. ; 116:7, s. 1913-1923
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Adenosine has been described as playing a role in the control of inflammation, but it has not been certain which of its receptors mediate this effect. Here, we generated an A2B adenosine receptor-knockout/reporter gene-knock-in (A2BAR-knockout/reporter gene-knock-in) mouse model and showed receptor gene expression in the vasculature and macrophages, the ablation of which causes low-grade inflammation compared with age-, sex-, and strain-matched control mice. Augmentation of proinflammatory cytokines, such as TNF-alpha, and a consequent downregulation of IkappaB-alpha are the underlying mechanisms for an observed upregulation of adhesion molecules in the vasculature of these A2BAR-null mice. Intriguingly, leukocyte adhesion to the vasculature is significantly increased in the A2BAR-knockout mice. Exposure to an endotoxin results in augmented proinflammatory cytokine levels in A2BAR-null mice compared with control mice. Bone marrow transplantations indicated that bone marrow (and to a lesser extent vascular) A2BARs regulate these processes. Hence, we identify the A2BAR as a new critical regulator of inflammation and vascular adhesion primarily via signals from hematopoietic cells to the vasculature, focusing attention on the receptor as a therapeutic target

Subject headings

NATURVETENSKAP  -- Geovetenskap och miljövetenskap -- Geokemi (hsv//swe)
NATURAL SCIENCES  -- Earth and Related Environmental Sciences -- Geochemistry (hsv//eng)

Keyword

Applied Geology
Tillämpad geologi

Publication and Content Type

ref (subject category)
art (subject category)

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