Home LiteratureArticle Details
PMID: 21958383 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

Platelet membrane phospholipid asymmetry: from the characterization of a scramblase activity to the identification of an essential protein mutated in Scott syndrome.

Journal of thrombosis and haemostasis : JTH ·Vol. 9 ·No. 10 ·2011-10-00 ·Pages 1883-91

Lhermusier T, Chap H, Payrastre B

Abstract

Like all eukaryotic cells, platelets maintain plasma membrane phospholipid asymmetry in normal blood circulation via lipid transporters, which control transbilayer movement. Upon platelet activation, the asymmetric orientation of membrane phospholipids is rapidly disrupted, resulting in a calcium-dependent exposure of the anionic phospholipid, phosphatidylserine (PS), at the outer platelet surface. This newly-exposed PS surface is a major component of normal hemostasis because it supports platelet procoagulant function. Binding of blood clotting enzyme complexes to this negatively-charged membrane surface allows a dramatic increase in the rate of conversion of zymogens to active serine proteases, which in turn produce a burst of thrombin leading to the formation of a fibrin clot and further platelet activation. Cells have the capacity to catalyze transbilayer phospholipid exchange via ATP-requiring translocase enzymes (flippases and floppases), which control unidirectional phospholipid transport against a concentration gradient. They also use an energy-independent, calcium-dependent scramblase activity to govern the bidirectional exchange of phospholipids between the two leaflets of the bilayer; this activity is essential for PS exposure during platelet activation. Scramblase activity, biochemically characterized in the 1980s, is deficient in patients with Scott syndrome, a rare inherited bleeding disorder with defective platelet procoagulant activity. Despite considerable efforts, the platelet scramblase protein remained elusive for years but a significant advance has recently been made with the identification of TMEM16F, a membrane protein essential for calcium-dependent PS exposure whose loss of function mutations are found in Scott syndrome. This review recalls historical aspects of platelet membrane asymmetry characterization, summarizes the mechanisms and roles of PS exposure following platelet activation and discusses the recent identification of TMEM16F and its significance in the scrambling process.

MeSH Terms
Apoptosis Blood Coagulation Disorders/genetics,metabolism Blood Platelets/metabolism Calcium/metabolism Humans Membrane Lipids/metabolism Mutation Phospholipid Transfer Proteins/genetics,metabolism Platelet Activation Syndrome
Chemicals
Membrane Lipids Phospholipid Transfer Proteins Calcium
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Lhermusier T
Inserm, U1048 and Université Toulouse 3, I2MC, 31432 Toulouse Cedex 04, France.
Chap H
Payrastre B
Article Info
Journal
Journal of thrombosis and haemostasis : JTH
Abbr.
J Thromb Haemost
ISSN
1538-7836
Published
2011-10-00
Pages
1883-91
Language
English
Region
England
NLM ID
101170508
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com