Erythrocyte P2X receptor expression is correlated with change in haematocrit in patients admitted to the ICU with blood pathogen-positive sepsis

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Erythrocyte P2X receptor expression is correlated with change in haematocrit in patients admitted to the ICU with blood pathogen-positive sepsis

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im August 2018 veröffentlichter wissenschaftlicher Artikel

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scientific article published on 02 August 2018

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wetenschappelijk artikel

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наукова стаття, опублікована в серпні 2018

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name

Erythrocyte P2X receptor expre ...... blood pathogen-positive sepsis

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Erythrocyte P2X receptor expre ...... blood pathogen-positive sepsis

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Erythrocyte P2X receptor expre ...... blood pathogen-positive sepsis

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Erythrocyte P2X receptor expre ...... blood pathogen-positive sepsis

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Erythrocyte P2X receptor expre ...... blood pathogen-positive sepsis

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Erythrocyte P2X receptor expre ...... blood pathogen-positive sepsis

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P1476

Erythrocyte P2X1 receptor expr ...... blood pathogen-positive sepsis

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Parth Patel

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Steen K Fagerberg

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Xiaowen Lui

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P2860

Epidemiology of severe sepsis in the United States: analysis of incidence, outcome, and associated costs of care

Oxygen consumption in sepsis and septic shock

Role of a disintegrin and metalloprotease 10 in Staphylococcus aureus alpha-hemolysin-mediated cellular injury

Differences in purinergic amplification of osmotic cell lysis by the pore-forming RTX toxins Bordetella pertussis CyaA and Actinobacillus pleuropneumoniae ApxIA: the role of pore size.

Alpha-hemolysin from Escherichia coli uses endogenous amplification through P2X receptor activation to induce hemolysis.

Escherichia coli alpha-hemolysin triggers shrinkage of erythrocytes via K(Ca)3.1 and TMEM16A channels with subsequent phosphatidylserine exposure.

Bacterial RTX toxins allow acute ATP release from human erythrocytes directly through the toxin pore.

Evidence for associations between the purinergic receptor P2X(7) (P2RX7) and toxoplasmosis

Python erythrocytes are resistant to α-hemolysin from Escherichia coli.

Regulation of P2X4 receptors by lysosomal targeting, glycan protection and exocytosis.

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s13054-018-2100-3

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181

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scholarly article

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10.1186/S13054-018-2100-3

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English

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Lars W Andersen

Helle A Praetorius

Michael W Donnino

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2018-08-02T00:00:00Z

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1105964063

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30071869

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6091015

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