Mediators of inflammation, Alarmins

From WikiLectures

Mediators of inflammation are substances that regulate the course of inflammatory reaction.

Among them we include:

Alarms[edit | edit source]

Substances that are released first during an inflammatory reaction (signal 0). Their function is primarily modulation of the immune response'. They are followed by cytokines and subsequently acute phase reactants.

Significant for earlier laboratory diagnosis of incipient inflammation than for acute phase reactants.

DAMPs (damage associated molecular patterns)[edit | edit source]

Molecules that are released from damaged cells for example during necrosis or other cell death (except apoptosis – phagocytosis of apoptotic bodies). It participates in the inflammatory reaction even when the microbe is no longer present.

These include, for example, ATP, DNA, RNA (extracellular usually not present), S100 proteins, HMGB1 (an intracellular protein capable of remodeling chromatin, usually produced by necrotic cells, macrophages, NK cells and dendritic cells), adenosine, uric acid.

PAMPs (pathogen associated molecular patterns)[edit | edit source]

Substances that are specific to microbes - dsRNA'' and bacterial DNA', lipopolysaccharide, lipoteichoic acid, 'peptidoglycan.

Receptors for alarmins - PRRs (pattern recognition receptors)[edit | edit source]

Very important receptors for the proper functioning of the immune system. They regulate the immune response', cell death or cell differentiation. They are proteins expressed on the surface of cells of the immune system (neutrophils, monocytes, macrophages, dendritic cells, epithelial cells). They recognize DAMPs and PAMPs molecules.

Toll-like receptors (TLR)[edit | edit source]

RAGE receptor

An extracellular receptor that is able to recognize foreign (potentially dangerous) structures. They occur mainly on the surface of cells of the immune system and surface epithelia. It belongs to the first line of defense against pathogens. Its stimulation leads to the production of cytokines and chemokines (activation of a specific immune response).

RAGE (receptor for advanced glycation end products)[edit | edit source]

A receptor for advanced glycation end products. It is a multiligand extracellular receptor capable of binding multiple alarmins. It is involved in a number of pathological conditions - inflammation, Alzheimer's disease, diabetic complications, complications of renal failure and vascular wall damage.

Physiologically, it participates in the development of muscles and bones in embryogenesis.

Nod-like receptors (NLRs)[edit | edit source]

Intracellular cytoplasmic proteins. After activation by phagocytosed bacterial peptidoglycans and cellular stress, they initiate an immune response.

Cytokines[edit | edit source]

Cytokine production after pathogen challenge

It serves to regulate the immune response. They are produced mainly by activated macrophages and T-helpers after stimulation by immune complexes or microbial products. Furthermore, they are important for the communication of cells of the immune system.

The main functions of cytokines include:

  • fever stimulation,
  • influence on the synthesis of acute phase reactants (in the liver),
  • complement activation, opsonization,
  • stimulation of myelopoiesis and release of leukocytes from the bone marrow,
  • increase in the synthesis of heat shock proteins (chaperones) – affecting the configuration of newly synthesized proteins.

Among the cytokines in the inflammatory reaction, we include mainly IL-1, IL-6, TNF-α' and others.

Searchtool right.svg For more information see Cytokines.

Links[edit | edit source]

Related Articles[edit | edit source]

Source[edit | edit source]

  • {{#switch: website

|book =

  Incomplete publication citation. KALOUSOVÁ,. Zánět [online] . 2014. Also available from <https://ulbld.lf1.cuni.cz/file/1607/zanet-material.pdf>. 

|collection =

  Incomplete citation of contribution in proceedings. KALOUSOVÁ,. Zánět [online] . 2014. Also available from <https://ulbld.lf1.cuni.cz/file/1607/zanet-material.pdf>. {{
  #if:  |978-80-7262-438-6} }
  |article = 
  Incomplete article citation.  KALOUSOVÁ,. 2014, year 2014, also available from <https://ulbld.lf1.cuni.cz/file/1607/zanet-material.pdf>. 

|web =

  Incomplete site citation. KALOUSOVÁ,. ©2014. [cit. 7/12/2018]. <https://ulbld.lf1.cuni.cz/file/1607/zanet-material.pdf>.

|cd =

  Incomplete carrier citation. KALOUSOVÁ,. ©2014. [cit. 7/12/2018]. 

|db =

  Incomplete database citation. ©2014. [cit. 7/12/2018]. <https://ulbld.lf1.cuni.cz/file/1607/zanet-material.pdf>.

|corporate_literature =

  Incomplete citation of company literature. KALOUSOVÁ,. Zánět [online] . 2014. Also available from <https://ulbld.lf1.cuni.cz/file/1607/zanet-material.pdf>. legislative_document = 
  Incomplete citation of legislative document.  2014. Also available from URL <https://ulbld.lf1.cuni.cz/file/1607/zanet-material.pdf>.


}}