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2233587 
Journal Article 
Mechanisms of hemolysis-associated platelet activation 
Helms, CC; Marvel, M; Zhao, W; Stahle, M; Vest, R; Kato, GJ; Lee, JS; Christ, G; Gladwin, MT; Hantgan, RR; Kim-Shapiro, DB 
2013 
Journal of Thrombosis and Haemostasis
ISSN: 1538-7933
EISSN: 1538-7836 
11 
12 
2148-2154 
English 
BACKGROUND: Intravascular hemolysis occurs after blood transfusion, in hemolytic anemias and other conditions, and is associated with hypercoagulable states. Hemolysis has been shown to potently activate platelets in vitro and in vivo and several mechanisms have been suggested to account for this including (1) direct activation by hemoglobin, (2) increase in reactive oxygen species (ROS), (3) scavenging of nitric oxide by released hemoglobin, and (4) release of intraerythrocytic ADP.

OBJECTIVE: The aim of the current study is to elucidate the mechanism of hemolysis-mediated platelet activation.

METHODS: We used flow cytometry to detect PAC-1 binding to activated platelets for in vitro experiments and a Siemens' Advia 120 hematology system to assess platelet aggregation using platelet counts from in vivo experiments in a rodent model.

RESULTS: We show that Hb does not directly activate platelets. However, ADP bound to Hb can cause platelet activation. Furthermore, platelet activation due to shearing of RBCs is reduced in the presence of apyrase which metabolizes ADP to AMP. Use of ROS scavengers did not affect platelet activation. We also show that cell free Hb does enhance platelet activation by abrogating the inhibitory effect of NO on platelet activation. In vivo infusions of ADP and purified (ADP-free) Hb as well as hemolysate result in platelet aggregation as evidenced by decreased platelet counts.

CONCLUSION: Two primary mechanisms account for red blood cell hemolysis-associated platelet activation: ADP release which activates platelets and cell-free hemoglobin release which enhances platelet activation by lowering NO bioavailability. This article is protected by copyright. All rights reserved. 
hemoglobin; hemolysis; nitric oxide; platelets; red blood cells