Back to Search
Start Over
The chaperone protein HSP47: a platelet collagen binding protein that contributes to thrombosis and hemostasis.
- Source :
-
Journal of thrombosis and haemostasis : JTH [J Thromb Haemost] 2018 May; Vol. 16 (5), pp. 946-959. Date of Electronic Publication: 2018 Apr 15. - Publication Year :
- 2018
-
Abstract
- Essentials Heat shock protein 47 (HSP47), a collagen specific chaperone is present on the platelet surface. Collagen mediated platelet function was reduced following blockade or deletion of HSP47. GPVI receptor regulated signalling was reduced in HSP47 deficient platelets. Platelet HSP47 tethers to exposed collagen thus modulating thrombosis and hemostasis.<br />Summary: Objective Heat shock protein 47 (HSP47) is an intracellular chaperone protein that is vital for collagen biosynthesis in collagen secreting cells. This protein has also been shown to be present on the surface of platelets. Given the importance of collagen and its interactions with platelets in triggering hemostasis and thrombosis, in this study we sought to characterize the role of HSP47 in these cells. Methods and Results The deletion of HSP47 in mouse platelets or its inhibition in human platelets reduced their function in response to collagen and the GPVI agonist (CRP-XL), but responses to thrombin were unaltered. In the absence of functional HSP47, the interaction of collagen with platelets was reduced, and this was associated with reduced GPVI-collagen binding, signalling and platelet activation. Thrombus formation on collagen, under arterial flow conditions, was also decreased following the inhibition or deletion of HSP47, in the presence or absence of eptifibatide, consistent with a role for HSP47 in enhancing platelet adhesion to collagen. Platelet adhesion under flow to von Willebrand factor was unaltered following HSP47 inhibition. Laser-induced thrombosis in cremaster muscle arterioles was reduced and bleeding time was prolonged in HSP47-deficient mice or following inhibition of HSP47. Conclusions Our study demonstrates the presence of HSP47 on the platelet surface, where it interacts with collagen, stabilizes platelet adhesion and increases collagen-mediated signalling and therefore thrombus formation and hemostasis.<br /> (© 2018 The Authors. Journal of Thrombosis and Haemostasis published by Wiley Periodicals, Inc. on behalf of International Society on Thrombosis and Haemostasis.)
- Subjects :
- Animals
Blood Platelets drug effects
Calcium Signaling
Carrier Proteins antagonists & inhibitors
Carrier Proteins genetics
Disease Models, Animal
HSP70 Heat-Shock Proteins antagonists & inhibitors
HSP70 Heat-Shock Proteins deficiency
HSP70 Heat-Shock Proteins genetics
Humans
Mice, Inbred C57BL
Mice, Knockout
Mitochondrial Proteins
Platelet Adhesiveness
Platelet Aggregation Inhibitors pharmacology
Platelet Membrane Glycoproteins metabolism
Protein Binding
Thrombosis genetics
Thrombosis prevention & control
Blood Platelets metabolism
Carrier Proteins blood
Collagen blood
HSP70 Heat-Shock Proteins blood
Hemostasis drug effects
Platelet Activation drug effects
Thrombosis blood
Subjects
Details
- Language :
- English
- ISSN :
- 1538-7836
- Volume :
- 16
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Journal of thrombosis and haemostasis : JTH
- Publication Type :
- Academic Journal
- Accession number :
- 29512284
- Full Text :
- https://doi.org/10.1111/jth.13998