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Thrombin-dependent intravascular leukocyte trafficking regulated by fibrin and the platelet receptors GPIb and PAR4
by
Ruggeri, Zaverio M.
, Kaplan, Zane S.
, Zarpellon, Alessandro
, McFadyen, James
, Jackson, Shaun P.
, Yuan, Yuping
, Schoenwaelder, Simone M.
, Ghasemzadeh, Mehran
, Alwis, Imala
in
14
/ 14/19
/ 59
/ 631/443/592/75/593
/ 631/80/313
/ 64
/ 64/110
/ 64/60
/ 692/308
/ 692/698/1543/1565/1597
/ Animals
/ Barriers
/ Cell Movement
/ Endothelial Cells - physiology
/ Fibrinolysis
/ Humanities and Social Sciences
/ Humans
/ Leukocytes - physiology
/ Male
/ Mice
/ Mice, Inbred C57BL
/ Models, Animal
/ multidisciplinary
/ Platelet Activation
/ Platelet Glycoprotein GPIb-IX Complex - metabolism
/ Receptors, Thrombin - metabolism
/ Science
/ Science (multidisciplinary)
/ Thrombin - metabolism
2015
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Thrombin-dependent intravascular leukocyte trafficking regulated by fibrin and the platelet receptors GPIb and PAR4
by
Ruggeri, Zaverio M.
, Kaplan, Zane S.
, Zarpellon, Alessandro
, McFadyen, James
, Jackson, Shaun P.
, Yuan, Yuping
, Schoenwaelder, Simone M.
, Ghasemzadeh, Mehran
, Alwis, Imala
in
14
/ 14/19
/ 59
/ 631/443/592/75/593
/ 631/80/313
/ 64
/ 64/110
/ 64/60
/ 692/308
/ 692/698/1543/1565/1597
/ Animals
/ Barriers
/ Cell Movement
/ Endothelial Cells - physiology
/ Fibrinolysis
/ Humanities and Social Sciences
/ Humans
/ Leukocytes - physiology
/ Male
/ Mice
/ Mice, Inbred C57BL
/ Models, Animal
/ multidisciplinary
/ Platelet Activation
/ Platelet Glycoprotein GPIb-IX Complex - metabolism
/ Receptors, Thrombin - metabolism
/ Science
/ Science (multidisciplinary)
/ Thrombin - metabolism
2015
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While trying to remove the title from your shelf something went wrong :( Kindly try again later!
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Thrombin-dependent intravascular leukocyte trafficking regulated by fibrin and the platelet receptors GPIb and PAR4
by
Ruggeri, Zaverio M.
, Kaplan, Zane S.
, Zarpellon, Alessandro
, McFadyen, James
, Jackson, Shaun P.
, Yuan, Yuping
, Schoenwaelder, Simone M.
, Ghasemzadeh, Mehran
, Alwis, Imala
in
14
/ 14/19
/ 59
/ 631/443/592/75/593
/ 631/80/313
/ 64
/ 64/110
/ 64/60
/ 692/308
/ 692/698/1543/1565/1597
/ Animals
/ Barriers
/ Cell Movement
/ Endothelial Cells - physiology
/ Fibrinolysis
/ Humanities and Social Sciences
/ Humans
/ Leukocytes - physiology
/ Male
/ Mice
/ Mice, Inbred C57BL
/ Models, Animal
/ multidisciplinary
/ Platelet Activation
/ Platelet Glycoprotein GPIb-IX Complex - metabolism
/ Receptors, Thrombin - metabolism
/ Science
/ Science (multidisciplinary)
/ Thrombin - metabolism
2015
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Thrombin-dependent intravascular leukocyte trafficking regulated by fibrin and the platelet receptors GPIb and PAR4
Journal Article
Thrombin-dependent intravascular leukocyte trafficking regulated by fibrin and the platelet receptors GPIb and PAR4
2015
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Overview
Thrombin is a central regulator of leukocyte recruitment and inflammation at sites of vascular injury, a function thought to involve primarily endothelial PAR cleavage. Here we demonstrate the existence of a distinct leukocyte-trafficking mechanism regulated by components of the haemostatic system, including platelet PAR4, GPIbα and fibrin. Utilizing a mouse endothelial injury model we show that thrombin cleavage of platelet PAR4 promotes leukocyte recruitment to sites of vascular injury. This process is negatively regulated by GPIbα, as seen in mice with abrogated thrombin-platelet GPIbα binding (
hGPIb
α
D277N
). In addition, we demonstrate that fibrin limits leukocyte trafficking by forming a physical barrier to intravascular leukocyte migration. These studies demonstrate a distinct ‘checkpoint’ mechanism of leukocyte trafficking involving balanced thrombin interactions with PAR4, GPIbα and fibrin. Dysregulation of this checkpoint mechanism is likely to contribute to the development of thromboinflammatory disorders.
Thrombin is a key proinflammatory protease regulating leukocyte trafficking at sites of vascular injury. Here the authors show that balanced thrombin interactions with platelet proteins PAR4, GPIbα and fibrin plays a major role in regulating this process.
Publisher
Nature Publishing Group UK,Nature Publishing Group
Subject
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