Vol 116, No 1 (Supplement) 2011
Supplement abstract

Hydroxytyrosol derivatives prevent apoptosis and autophagy

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  • Sabrina Burattini,
  • Sara Salucci,
  • Valentina Baldassarri,
  • Augusto Accorsi,
  • Manila Candiracci,
  • Giovanni Piersanti,
  • Jose L. Espartero Sanchez,
  • Giovanni Zappia,
  • Elisabetta Falcieri

Published 2011-11-23

Keywords

  • apoptosis,
  • autophagy,
  • C2C12 and U937 cells,
  • H2O2,
  • HT

How to Cite

Burattini, S., Salucci, S., Baldassarri, V., Accorsi, A., Candiracci, M., Piersanti, G., Espartero Sanchez, J. L., Zappia, G., & Falcieri, E. (2011). Hydroxytyrosol derivatives prevent apoptosis and autophagy. Italian Journal of Anatomy and Embryology, 116(2), 225. Retrieved from https://oajournals.fupress.net/index.php/ijae/article/view/4776
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Abstract

Hydroxytyrosol (HT) is released primarily in olive mill wastewater and in olive oil (Fabiani et al., 2008).
In animal and cellular model studies, HT and its metabolites show strong antioxidant and antimicrobial properties, as well as beneficial effects on the cardio-vascular system and in several human diseases (Goya et al., 2007). Differently, many reports in tumor cells (Han et al., 2009) suggested that HT down-regulates cell viability and proliferation, and induces apoptosis.
Nevertheless, little is known about its effect on normal cell apoptosis. Previous biochemical studies suggested that HT and HT derivatives, in particular the HT-Laurate (Laur-HT), show antioxidants effects on human erythrocytes (Manna et al.,1999).
In this study, we have investigated the effect of 20µM HT and 5µM Laur-HT in C2C12 myoblasts, a murine proliferating cell model, and U937 cells, a human monocytoid tumor cell line. H2O2, at the concentrations (0.5 and 1 mM) known to induce apoptotic death (Salucci et al., 2010), was utilized as cell death trigger.
Cell response was analysed by reverted (RM), light (LM) and transmission electron microscopy (TEM). Both cell lines observed at RM and LM showed a good morphology, in control condition. On the other hand, HT and Laur-HT, added to the control cells, did not influence cell viability.
After H2O2-treatment, the characteristic apoptotic features (D’Emilio et al., 2010) appeared at ultrastructural analysis in both cell models. Nevertheless, myoblasts exposed to 0.5 mM H2O2 presented a scarce response.  For this reason,  skeletal muscle apoptosis was investigated  using H2O2 at major concentration (1mM) that evidenced an apoptotic cell number increase, as well as a relevant presence of autophagic vacuoles (Zhang et al., 2009).
Their pre-incubation with HT and Laur-HT  prevented, in general, cell death and both apoptotic and autophagic patterns (Feng et al., 2011), as furtherly demonstrated by statistical analysis.
The anti-apoptotic and anti-autophagic action of these compounds, both on normal myoblasts and on tumor cells could represent an interesting property with potential biological and clinical applications.
Further studies are in progress in other cell models.

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