4.2 Article

Phosphatidylserine Exposure in Human Red Blood Cells Depending on Cell Age

Journal

CELLULAR PHYSIOLOGY AND BIOCHEMISTRY
Volume 38, Issue 4, Pages 1376-1390

Publisher

KARGER
DOI: 10.1159/000443081

Keywords

Red blood cells; Red blood cell age; Ca2+ content; Phosphatidylserine exposure; Lysophosphatidic acid; Phorbol-12 myristate-13 acetate; Flow cytometry; Fluorescence imaging

Funding

  1. Vietnam National Foundation for Science and Technology Development (NAFOSTED) [106-YS.06-2013.16]
  2. CNPq program science without borders [202426/2012-2]

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Background/Aims: The exposure of phosphatidylserine (PS) on the outer membrane leaflet of red blood cells (RBCs) serves as a signal for suicidal erythrocyte death or eryptosis, which may be of importance for cell clearance from blood circulation. PS externalisation is realised by the scramblase activated by an increase of intracellular Ca2+ content. It has been described in literature that RBCs show an increased intracellular Ca2+ content as well as PS exposure when becoming aged up to 120 days (which is their life span). However, these investigations were carried out after incubation of the RBCs for 48 h. The aim of this study was to investigate this effect after short-time incubation using a variety of stimulating substances for Ca2+ uptake and PS exposure. Methods: We separated RBCs by age in five different fractions by centrifugation using Percoll density gradient. The intracellular Ca2+ content and the PS exposure of RBCs with different age has been investigated after treatment with lysophosphatidic acid (LPA) as well as after activation of protein kinase C (PKC) using phorbol-12 myristate-13 acetate (PMA). For positive control RBCs were treated with 4-bromo-A23187. Measurement techniques included flow cytometry and live cell imaging (fluorescence microscopy). Results: The percentage of RBCs showing increased Ca2+ content as well as the PS exposure did not change significantly in dependence on cell age after short-time incubation in control experiments (without stimulating substances) or using LPA or PMA. However, we confirm findings reported that Ca2+ content and the PS exposure of RBCs increased after 48 h incubation. Conclusion: No significant differences of intracellular Ca2+ content and PS exposure can be seen for RBCs of different age in resting state or after stimulation of Ca2+ uptake at short-time incubation. (C) 2016 The Author(s)) Published by S Karger AG, Basel

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