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Platelet-activating factor
PAF-platelet activating factor.png
Identifiers
CAS number 74389-68-7
PubChem 108156
MeSH Platelet+Activating+Factor
Properties
Molecular formula C26H54NO7P
Molar mass 523.68 g mol−1
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

Platelet-activating factor, also known as a PAF, PAF-acether or AGEPC (acetyl-glyceryl-ether-phosphorylcholine) is a potent phospholipid activator and mediator of many leukocyte functions, including platelet aggregation, inflammation, and anaphylaxis.

It is produced in response to specific stimuli by a variety of cell types, including neutrophils, basophils, platelets, and endothelial cells.

Contents

[edit] Chemistry

Several molecular species of platelet-activating factor have been identified which vary in the length of the O-alkyl side chain.

  • Its alkyl group is connected by an ether linkage at the C1 carbon to a sixteen carbon chain.
  • The acyl group at the C2 carbon is an acetate unit (as opposed to a fatty acid) whose short length increases the solubility of PAF, allowing it to function as a soluble signal messenger.
  • The C3 has a phosphocholine head group, just like standard phosphatidylcholine.

[edit] Function

It is an important mediator of bronchoconstriction.

It causes platelets to aggregate and blood vessels to dilate. Thus it is important to the process of hemostasis. At a concentration of 10^-12 M, PAF causes life threatening inflammation of the airways to induce asthma like symptoms.

Toxins such as fragments of destroyed bacteria induce the synthesis of PAF, which causes a drop in blood pressure and reduced volume of blood pumped by the heart, which leads to shock and maybe death.

[edit] History

It was discovered by French immunologist Jacques Benveniste in the early 1970s.[1][2] Its structure was elucidated by Constantinos A. Demopoulos in 1979.[3]

[edit] Biosynthesis and degradation

PAF is biosynthesized from lysophosphatidylcholine (LPC) and acetyl CoA by the enzyme LPC acetyltransferase (LPCAT).

It is degraded (thereby terminating its capacity to act as a signaling molecule) by a group of enzymes called PAF acetylhydrolases (PAFAHs) which are related to phospholipase A2.

[edit] Antagonists

[edit] See also

[edit] References

  1. ^ Benveniste J, Henson PM, Cochrane CG (1972). "Leukocyte-dependent histamine release from rabbit platelets. The role of IgE, basophils, and a platelet-activating factor". J. Exp. Med. 136 (6): 1356–77. doi:10.1084/jem.136.6.1356. PMID 4118412. 
  2. ^ Benveniste J (1974). "Platelet-activating factor, a new mediator of anaphylaxis and immune complex deposition from rabbit and human basophils". Nature 249 (457): 581–2. doi:10.1038/249581a0. PMID 4275800. 
  3. ^ Demopoulos CA, Pinckard RN, Hanahan DJ (1979). "Platelet-activating factor. Evidence for 1-O-alkyl-2-acetyl-sn-glyceryl-3-phosphorylcholine as the active component (a new class of lipid chemical mediators)" (abstract). J. Biol. Chem. 254 (19): 9355–8. PMID 489536. http://www.jbc.org/cgi/content/abstract/254/19/9355. 
  4. ^ Platelet-Activating Factor Antagonist, SM-12502, Attenuates ...

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