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Acidosis downregulates platelet haemostatic functions and promotes neutrophil proinflammatory responses mediated by platelets

Etulain, Julia et al · Schattauer Gmbh-Verlag Medizin Naturwissenschaften · 2012

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Acidosis is one of the hallmarks of tissue injury such as trauma, infection, inflammation, and tumour growth. Although platelets participate in the pathophysiology of all these processes, the impact of acidosis on platelet biology has not been studied outside of the quality control of laboratory aggregation assays or platelet transfusion optimization. Herein, we evaluate the effect of physiologically relevant changes in extracellular acidosis on the biological function of platelets, placing particular emphasis on haemostatic and secretory functions. Platelet haemostatic responses such as adhesion, spreading, activation of αIIbβ3 integrin, ATP release, aggregation, thromboxane B2 generation, clot retraction and procoagulant activity including phosphatidilserine exposure and microparticle formation, showed a statistically significant inhibition of thrombin-induced changes at pH of 7.0 and 6.5 compared to the physiological pH (7.4). The release of alpha granule content was differentially regulated by acidosis. At low pH, thrombin or collagen-induced secretion of vascular endothelial growth factor and endostatin were dramatically reduced. The release of von Willebrand factor and stromal derived factor-1α followed a similar, albeit less dramatic pattern. In contrast, the induction of CD40L was not changed by low pH, and P-selectin exposure was significantly increased. While the generation of mixed platelet-leukocyte aggregates and the increased chemotaxis of neutrophils mediated by platelets were further augmented under acidic conditions in a P-selectin dependent manner, the increased neutrophil survival was independent of P-selectin expression. In conclusion, our results indicate that extracellular acidosis downregulates most of the haemostatic platelet functions, and promotes those involved in amplifying the neutrophil-mediated inflammatory response. Fil: Etulain, Julia. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Medicina Experimental. Academia Nacional de Medicina de Buenos Aires. Instituto de Medicina Experimental; Argentina. Academia Nacional de Medicina de Buenos Aires. Instituto de Investigaciones Hematológicas "Mariano R. Castex". Departamento de Hemostasia y Trombosis; Argentina Fil: Negrotto, Soledad. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Medicina Experimental. Academia Nacional de Medicina de Buenos Aires. Instituto de Medicina Experimental; Argentina. Academia Nacional de Medicina de Buenos Aires. Instituto de Investigaciones Hematológicas "Mariano R. Castex". Departamento de Hemostasia y Trombosis; Argentina

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APA 7

Etulain, J. E. A. (2012). Acidosis downregulates platelet haemostatic functions and promotes neutrophil proinflammatory responses mediated by platelets. http://hdl.handle.net/11336/268719

MLA

Etulain, Julia et al. "Acidosis downregulates platelet haemostatic functions and promotes neutrophil proinflammatory responses mediated by platelets." 2012. http://hdl.handle.net/11336/268719.

Chicago

Etulain, Julia et al. 2012. "Acidosis downregulates platelet haemostatic functions and promotes neutrophil proinflammatory responses mediated by platelets.". http://hdl.handle.net/11336/268719.

Harvard

Etulain, J. E. A. 2012, Acidosis downregulates platelet haemostatic functions and promotes neutrophil proinflammatory responses mediated by platelets, Schattauer Gmbh-Verlag Medizin Naturwissenschaften, available at: http://hdl.handle.net/11336/268719 [Accessed 6 Aug. 2026].

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Título
Acidosis downregulates platelet haemostatic functions and promotes neutrophil proinflammatory responses mediated by platelets
Autor / colaboradores
Etulain, Julia et al
Editorial
Schattauer Gmbh-Verlag Medizin Naturwissenschaften
Año de publicación
2012
ISSN
0340-6245
ISSN
0340-6245
Idioma
Inglés

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