Cd14

Author:Prof. Dr. med. Peter Altmeyer

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Last updated on: 26.04.2024

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Synonym(s)

LPS receptor

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DefinitionThis section has been translated automatically.

Markers for: monocytes, macrophages, Langerhans cells, dendritic cells; also B cells and neutrophils.

Structure: Surface membrane protein (53-55 kDa)

Note: CD14 acts as an affinity receptor for the complex of lipopolysaccharides (LPS) and LPS binding protein (LBP).

Application: FACS, IHC (P) (G), IF

(see below) Cluster of differentiation

General informationThis section has been translated automatically.

CD14 is a glycosylphosphatidylinositol-anchored protein that is mainly expressed on monocytes and macrophages. CD14 is also expressed on neutrophils and granulocytes, but to a much lesser extent. The corresponding human CD14 gene consists of two exons and is located on chromosome five. The corresponding encoded protein consists of 356 amino acids, mainly leucine repeats. A mutation of amino acids 39 to 44 inclusive leads to a loss of the ability to bind LPS. A proportion of 3-4 µg/ml of the CD14 receptors is present as a soluble, free portion in the serum and is therefore able to bind LPS at an early stage, thus blocking cellular activation.

The CD14 receptor is a monocyte differentiation antigen that falls into the category of pattern recognition receptors. When the CD14 receptor was initially discovered, it was doubted that it could participate in an intracellular signaling cascade due to its lack of an intracellular component. It was later recognized that CD14 is a co-receptor for the TLR4 signaling pathway. The CD14 receptor can therefore be regarded as a component of the innate immune response. Furthermore, the receptor was also recognized as a transport protein of inflammatory lipids to initiate phagocytosis.

LiteratureThis section has been translated automatically.

  1. Hantschke M et al (2016) Immunohistological techniques. In: L. Cerroni et al. histopathology of the skin. Springer publishing house Berlin-Heidelberg p. 26-33.

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Last updated on: 26.04.2024