TY - JOUR
T1 - The plant decapeptide OSIP108 prevents copper-induced apoptosis in yeast and human cells
AU - Spincemaille, Pieter
AU - Chandhok, Gursimran
AU - Newcomb, Benjamin
AU - Verbeek, Jef
AU - Vriens, Kim
AU - Zibert, Andree
AU - Schmidt, Hartmut
AU - Hannun, Yusuf A.
AU - van Pelt, Jos
AU - Cassiman, David
AU - Cammue, Bruno P.A.
AU - Thevissen, Karin
PY - 2014/6
Y1 - 2014/6
N2 - We previously identified the Arabidopsis thaliana-derived decapeptide OSIP108, which increases tolerance of plants and yeast cells to oxidative stress. As excess copper (Cu) is known to induce oxidative stress and apoptosis, and is characteristic for the human pathology Wilson disease, we investigated the effect of OSIP108 on Cu-induced toxicity in yeast. We found that OSIP108 increased yeast viability in the presence of toxic Cu concentrations, and decreased the prevalence of Cu-induced apoptotic markers. Next, we translated these results to the human hepatoma HepG2 cell line, demonstrating anti-apoptotic activity of OSIP108 in this cell line. In addition, we found that OSIP108 did not affect intracellular Cu levels in HepG2 cells, but preserved HepG2 mitochondrial ultrastructure. As Cu is known to induce acid sphingomyelinase activity of HepG2 cells, we performed a sphingolipidomic analysis of OSIP108-treated HepG2 cells. We demonstrated that OSIP108 decreased the levels of several sphingoid bases and ceramide species. Moreover, exogenous addition of the sphingoid base dihydrosphingosine abolished the protective effect of OSIP108 against Cu-induced cell death in yeast. These findings indicate the potential of OSIP108 to prevent Cu-induced apoptosis, possibly via its effects on sphingolipid homeostasis.
AB - We previously identified the Arabidopsis thaliana-derived decapeptide OSIP108, which increases tolerance of plants and yeast cells to oxidative stress. As excess copper (Cu) is known to induce oxidative stress and apoptosis, and is characteristic for the human pathology Wilson disease, we investigated the effect of OSIP108 on Cu-induced toxicity in yeast. We found that OSIP108 increased yeast viability in the presence of toxic Cu concentrations, and decreased the prevalence of Cu-induced apoptotic markers. Next, we translated these results to the human hepatoma HepG2 cell line, demonstrating anti-apoptotic activity of OSIP108 in this cell line. In addition, we found that OSIP108 did not affect intracellular Cu levels in HepG2 cells, but preserved HepG2 mitochondrial ultrastructure. As Cu is known to induce acid sphingomyelinase activity of HepG2 cells, we performed a sphingolipidomic analysis of OSIP108-treated HepG2 cells. We demonstrated that OSIP108 decreased the levels of several sphingoid bases and ceramide species. Moreover, exogenous addition of the sphingoid base dihydrosphingosine abolished the protective effect of OSIP108 against Cu-induced cell death in yeast. These findings indicate the potential of OSIP108 to prevent Cu-induced apoptosis, possibly via its effects on sphingolipid homeostasis.
KW - Apoptosis
KW - Ceramide
KW - Copper
KW - OSIP108
KW - Saccharomyces cerevisiae
UR - http://www.scopus.com/inward/record.url?scp=84897831558&partnerID=8YFLogxK
U2 - 10.1016/j.bbamcr.2014.03.004
DO - 10.1016/j.bbamcr.2014.03.004
M3 - Article
C2 - 24632503
AN - SCOPUS:84897831558
SN - 0167-4889
VL - 1843
SP - 1207
EP - 1215
JO - BBA Molecular Cell Research
JF - BBA Molecular Cell Research
IS - 6
ER -