Alterations of hemorheological parameters and tubulin content in erythrocytes from diabetic subjects

[Display omitted] •High glucose promote in erythrocytes translocation of tubulin to the membrane.•Membrane tubulin regulates erythrocyte deformability and osmotic fragility.•High glucose concentrations induce increases of acetylation of tubulin.•Tubulin acetylation resulted from inhibition of deacet...

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Published inThe international journal of biochemistry & cell biology Vol. 74; pp. 109 - 120
Main Authors Nigra, Ayelén D., Monesterolo, Noelia E., Rivelli, Juan F., Amaiden, Marina R., Campetelli, Alexis N., Casale, Cesar H., Santander, Verónica S.
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier Ltd 01.05.2016
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Summary:[Display omitted] •High glucose promote in erythrocytes translocation of tubulin to the membrane.•Membrane tubulin regulates erythrocyte deformability and osmotic fragility.•High glucose concentrations induce increases of acetylation of tubulin.•Tubulin acetylation resulted from inhibition of deacetylase enzymes.•The mechanism explains involvement of tubulin in diabetes. Treatment of human erythrocytes with high glucose concentrations altered the content and distributions of three tubulin isotypes, with consequent reduction of erythrocyte deformability and osmotic resistance. In erythrocytes from diabetic subjects (D erythrocytes), (i) tubulin in the membrane-associated fraction (Mem-Tub) was increased and tubulin in the sedimentable fraction (Sed-Tub) was decreased, (ii) deformability was lower than in erythrocytes from normal subjects (N erythrocytes), and (iii) detyrosinated/acetylated tubulin content was higher in the Mem-Tub fraction and tyrosinated/acetylated tubulin content was higher in the Sed-Tub fraction, in comparison with N erythrocytes. Similar properties were observed for human N erythrocytes treated with high glucose concentrations, and for erythrocytes from rats with streptozotocin-induced diabetes. In N erythrocytes, high-glucose treatment caused translocation of tubulin from the Sed-Tub to Mem-Tub fraction, thereby reducing deformability and inducing acetylation/tyrosination in the Sed-Tub fraction. The increased tubulin acetylation in these cells resulted from inhibition of deacetylase enzymes. Increased tubulin acetylation and translocation of this acetylated tubulin to the Mem-Tub fraction were both correlated with reduced osmotic resistance. Our findings suggest that (i) high glucose concentrations promote tubulin acetylation and translocation of this tubulin to the membrane, and (ii) this tubulin is involved in regulation of erythrocyte deformability and osmotic fragility.
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ISSN:1357-2725
1878-5875
DOI:10.1016/j.biocel.2016.02.016