4.5 Article

Tumor necrosis factor α-converting enzyme (TACE/ADAM17) mediates ectodomain shedding of the scavenger receptor CD163

Journal

JOURNAL OF LEUKOCYTE BIOLOGY
Volume 88, Issue 6, Pages 1201-1205

Publisher

WILEY
DOI: 10.1189/jlb.0410235

Keywords

endocytosis; hemoglobin; pathogenesis; sepsis; macrophage

Funding

  1. Danish Medical Research Council
  2. Novo Nordisk Foundation
  3. European Reseach Council
  4. Lundbeck Foundation

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CD163 is expressed specifically in the monocyte/macrophage lineage, where it mediates uptake of haptoglobin- hemoglobin complexes, leading to metabolism of the oxidative heme molecule. Shedding of the CD163 ectodomain from the cell surface produces a sCD163 plasma protein, and a positive correlation is seen between the sCD163 plasma level and the severity of various infectious and inflammatory diseases. In the present analysis of the phorbol ester-induced shedding of sCD163 in CD163 cDNA-transfected HEK293 cells, we used metalloproteinase inhibitors and siRNA-mediated inhibition of metalloproteinases to identify TACE/ADAM17 as an enzyme responsible for PMA-induced cleavage of the membrane-proximal region of CD163. As TACE/ADAM17-mediated shedding of TNF-alpha is up-regulated in macrophages subjected to inflammatory stimuli, the present results now provide a likely explanation for the strong empirical relationship between the sCD163 plasma level and infectious/inflammatory diseases relating to macrophage activity. J. Leukoc. Biol. 88: 1201-1205; 2010.

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