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CD14, new aspects of ligand and signal diversity

R Landmann1, B Müller, W Zimmerli

  • 1Division of Infectious Diseases, Departments of Research and Internal Medicine, University Hospital, Hebelstrasse 20, 4031, Basel, Switzerland.

Microbes and Infection
|April 12, 2000
PubMed

Insights

Glycosyl-phosphatidylinositol-linked glycoprotein CD14 (CD14) binds bacterial components and phospholipids, mediating inflammatory signals. Its altered expression in inflammatory diseases suggests a pathogenic role for this microbial receptor.

Area of Science:

  • Immunology
  • Molecular Biology
  • Cell Biology

Background:

  • Glycosyl-phosphatidylinositol-linked glycoprotein CD14 (CD14) is expressed on myeloid cells and in serum.
  • CD14 acts as a receptor for bacterial cell wall components (Gram-negative and -positive) and endogenous phospholipids.
  • CD14 signaling involves Toll-like receptors, NF-kappaB, and MAP kinases, playing a role in inflammation.

Purpose of the Study:

  • To elucidate the role of CD14 in inflammatory processes.
  • To investigate the molecular mechanisms underlying CD14-mediated signaling.
  • To explore the implications of CD14 alterations in inflammatory diseases.

Main Methods:

  • Expression analysis of CD14 in myeloid cells and serum.
  • Biochemical assays to study CD14 binding to bacterial components and phospholipids.
  • Cellular signaling pathway analysis involving Toll-like receptors, NF-kappaB, and MAP kinases.

Main Results:

  • CD14 expression confirmed in myeloid cells and serum.
  • Demonstrated binding of CD14 to diverse bacterial cell wall components and phospholipids.
  • Identified participation of Toll-like receptors, NF-kappaB, and MAP kinases in CD14 signaling pathways.

Conclusions:

  • CD14 is a key mediator in the inflammatory response to microbial products.
  • Alterations in CD14 expression and function are linked to inflammatory diseases.
  • CD14 represents a potential therapeutic target for inflammatory conditions.

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