New explanations for old observations: marginal band coiling during platelet activation

被引:34
作者
Sadoul, K. [1 ,2 ,3 ]
机构
[1] Univ Grenoble Alpes, IAB, F-38000 Grenoble, France
[2] INSERM, IAB, Grenoble, France
[3] CHU Grenoble, IAB, F-38043 Grenoble, France
关键词
actomyosin; blood platelets; cytoskeleton; microtubules; molecular motor proteins; THROMBIN-STIMULATED PLATELETS; HUMAN-BLOOD PLATELETS; ALPHA-TUBULIN ACETYLTRANSFERASE; SHAPE CHANGE; CYTOSKELETAL REORGANIZATION; POSTTRANSLATIONAL MODIFICATIONS; CYTOPLASMIC DYNEIN; MICROTUBULE COILS; INTERMEDIATE-FILAMENTS; INTERNAL CONTRACTION;
D O I
10.1111/jth.12819
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Blood platelets are tiny cell fragments derived from megakaryocytes. Their primary function is to control blood vessel integrity and ensure hemostasis if a vessel wall is damaged. Circulating quiescent platelets have a flat, discoid shape maintained by a circumferential microtubule bundle, called the marginal band (MB). In the case of injury platelets are activated and rapidly adopt a spherical shape due to microtubule motor-induced elongation and subsequent coiling of the MB. Platelet activation and shape change can be transient or become irreversible. This depends on the strength of the activation stimulus, which is translated into a cytoskeletal crosstalk between microtubules, their motors and the actomyosin cortex, ensuring stimulus-response coupling. Following microtubule motor-driven disc-to-sphere transition, a strong stimulus will lead to compression of the sphere through actomyosin cortex contraction. This will concentrate the granules in the center of the platelet and accelerate their exocytosis. Once granules are released, platelets have crossed the point of no return to irreversible activation. This review summarizes the current knowledge of the molecular mechanism leading to platelet shape change, with a special emphasis on microtubules, and refers to previously published observations, which have been essential for generating an integrated view of cytoskeletal rearrangements during platelet activation.
引用
收藏
页码:333 / 346
页数:14
相关论文
共 100 条
[61]   The spectrin-based membrane skeleton stabilizes mouse megakaryocyte membrane systems and is essential for proplatelet and platelet formation [J].
Patel-Hett, Sunita ;
Wang, Hongbei ;
Begonja, Antonija J. ;
Thon, Jonathan N. ;
Alden, Eva C. ;
Wandersee, Nancy J. ;
An, Xiuli ;
Mohandas, Narla ;
Hartwig, John H. ;
Italiano, Joseph E., Jr. .
BLOOD, 2011, 118 (06) :1641-1652
[62]   Dynamic regulation of microtubule coils in ADP-induced platelet shape change by p160ROCK (Rho-kinase) [J].
Paul, BZS ;
Kim, S ;
Dangelmaier, C ;
Nagaswami, C ;
Jin, JG ;
Hartwig, JH ;
Weisel, JW ;
Daniel, JL ;
Kunapuli, SP .
PLATELETS, 2003, 14 (03) :159-169
[63]   Human atheromatous plaques stimulate thrombus formation by activating platelet glycoprotein VI [J].
Penz, S ;
Reininger, AJ ;
Brandl, R ;
Goyal, P ;
Rabie, T ;
Bernlochner, I ;
Rother, E ;
Goetz, C ;
Engelmann, B ;
Smethurst, PA ;
Ouwehand, WH ;
Farndale, R ;
Nieswandt, B ;
Siess, W .
FASEB JOURNAL, 2005, 19 (08) :898-909
[64]   Megakaryocyte-specific RhoA deficiency causes macrothrombocytopenia and defective platelet activation in hemostasis and thrombosis [J].
Pleines, Irina ;
Hagedorn, Ina ;
Gupta, Shuchi ;
May, Frauke ;
Chakarova, Lidija ;
van Hengel, Jolanda ;
Offermanns, Stefan ;
Krohne, Georg ;
Kleinschnitz, Christoph ;
Brakebusch, Cord ;
Nieswandt, Bernhard .
BLOOD, 2012, 119 (04) :1054-1063
[65]   Proteomic and Phospho-Proteomic Profile of Human Platelets in Basal, Resting State: Insights into Integrin Signaling [J].
Qureshi, Amir H. ;
Chaoji, Vineet ;
Maiguel, Dony ;
Faridi, Mohd Hafeez ;
Barth, Constantinos J. ;
Salem, Saeed M. ;
Singhal, Mudita ;
Stoub, Darren ;
Krastins, Bryan ;
Ogihara, Mitsunori ;
Zaki, Mohammed J. ;
Gupta, Vineet .
PLOS ONE, 2009, 4 (10)
[66]   Molecular Adaptations Allow Dynein to Generate Large Collective Forces inside Cells [J].
Rai, Arpan K. ;
Rai, Ashim ;
Ramaiya, Avin J. ;
Jha, Rupam ;
Mallik, Roop .
CELL, 2013, 152 (1-2) :172-182
[67]   Determination of Critical Parameters in Platelet Margination [J].
Reasor, Daniel A., Jr. ;
Mehrabadi, Marmar ;
Ku, David N. ;
Aidun, Cyrus K. .
ANNALS OF BIOMEDICAL ENGINEERING, 2013, 41 (02) :238-249
[68]  
Rothwell SW, 1997, THROMB HAEMOSTASIS, V78, P910
[69]   CHARACTERIZATION OF THE POSTTRANSLATIONAL MODIFICATIONS IN TUBULIN FROM THE MARGINAL BAND OF AVIAN ERYTHROCYTES [J].
RUDIGER, M ;
WEBER, K .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1993, 218 (01) :107-116
[70]   HDAC6 controls the kinetics of platelet activation [J].
Sadoul, Karin ;
Wang, Jin ;
Diagouraga, Boubou ;
Vitte, Anne-Laure ;
Buchou, Thierry ;
Rossini, Therese ;
Polack, Benoit ;
Xi, Xiaodong ;
Matthias, Patrick ;
Khochbin, Saadi .
BLOOD, 2012, 120 (20) :4215-4218