Involvement of microtubules in the tolerance of cardiomyocytes to cold ischemia-reperfusion

• Published in: Molecular and cellular biochemistry 2008-01, Vol.307 (1-2), p.149-157
• Main Authors: Devillard, Lisa, Vandroux, David, Tissier, Cindy, Dumont, Laure, Borgeot, Jessica, Rochette, Luc, Athias, Pierre
• Format: Article
• Language: English
• Subjects: Acetylation; Acetyltransferases - metabolism; Animals; Animals, Newborn; Biochemistry; Biomedical and Life Sciences; Cardiology; Cardiomyocytes; Cells, Cultured; Cold Ischemia - adverse effects; Cytoprotection - drug effects; Dimerization; Docetaxel; Free Radicals - metabolism; Hypothermia; Hypothermia - pathology; Ischemia; Life Sciences; Low temperature; Medical Biochemistry; microtubules; Microtubules - physiology; Myocytes, Cardiac - drug effects; Myocytes, Cardiac - metabolism; Myocytes, Cardiac - pathology; Neonatal rats; Oncology; Oxidation; Oxidative stress; Oxidative Stress - drug effects; Oxidative Stress - physiology; Protein Binding; Rats; Rats, Wistar; Reperfusion Injury - metabolism; Reperfusion Injury - pathology; Simulated ischemia-reperfusion; Taxoids - pharmacology; Tubulin - metabolism
• ISSN: 0300-8177; 1573-4919
• DOI: 10.1007/s11010-007-9594-3

Before transplantation, the heart graft is preserved by the use of cold storage in order to limit ischemia-reperfusion stress. However, sustained exposure to low temperature may induce myocardial ultrastructural damage, particularly microtubules (MT) disruption. Previous data suggested that tubulin-binding agents are able to attenuate cold-induced cytoskeleton alterations. Thus, the aim of the present work was to study the influence of docetaxel (DX, a tubulin-binding taxane) on the effects of deep hypothermia (4°C) and of simulated cold ischemia-reperfusion on the MT network and oxidative stress of cardiomyocyte (CM) in monolayer cultures prepared from newborn rat ventricles. The MT network was explored by immunocytochemistry and Western-blotting, the cell stress by tetrazolium dye assay (MTT) and lactate dehydrogenase (LDH) release, and the superoxide production by the dihydroethidium probe (DHE). The MT assembly remained stable after 4 and 8 h of hypothermia. Tubulin acetylation was promoted in CM subjected to 4-h hypothermia. Low temperature reduced the mitochondrial function and increased the basal LDH release. The cold ischemia during 4 and 8 h preserved MT network. Docetaxel promoted MT polymerization and tubulin acetylation in basal and in cold conditions. This drug decreased the release of LDH induced by cold ischemia. Moreover, hypothermia (4 h) significantly raised the anion superoxide production. Docetaxel decreased this oxidative stress in the control CM and in CM submitted to 4 h of hypothermia. These data demonstrated that stabilizing MT with DX exerted a protective effect on CM subjected to hypothermia and to cold ischemia-reperfusion. Tubulin-ligands should be thus considered to improve the tolerance of the heart graft toward stressing conservative conditions.