2008
Response of normal vs. cancer colon cells to short- and long-chain fatty acids
KOUBKOVÁ, Zuzana; Jiřina HOFMANOVÁ; Miroslav CIGÁNEK; Josef SLAVÍK; Belma SKENDER et al.Základní údaje
Originální název
Response of normal vs. cancer colon cells to short- and long-chain fatty acids
Autoři
KOUBKOVÁ, Zuzana; Jiřina HOFMANOVÁ; Miroslav CIGÁNEK; Josef SLAVÍK; Belma SKENDER; Miroslav MACHALA a Alois KOZUBÍK
Vydání
Response of normal vs. cancer colon cells to short- and long-chain fatty acids ISAC XXIV International Congress, Cytometry in the Age of Systems Biology, Budapest, Hungary, 2008
Další údaje
Jazyk
angličtina
Typ výsledku
Konferenční abstrakt
Obor
30105 Physiology
Stát vydavatele
Česká republika
Utajení
není předmětem státního či obchodního tajemství
Označené pro přenos do RIV
Ano
Kód RIV
RIV/00216224:14310/08:00060308
Organizační jednotka
Přírodovědecká fakulta
Klíčová slova anglicky
polyunsaturated fatty acids sodium butyrate colon cancer
Změněno: 4. 1. 2013 15:46, Mgr. Belma Skender, Ph.D.
Anotace
V originále
Dynamic balance between proliferation, differentiation and apoptosis is necessary for healthy intestinal epithelium. Together with endogenous regulators dietary lipid compounds like esential polyunsaturated fatty acids (PUFAs) and short chain fatty acid – butyrate (produced by microbial fermentation of fibre) can play an important role in maintaining homeostasis in this tissue. Signals induced by these factors are integrated inside the cells and may have significant impact on cell metabolism and kinetics. Processes of colon cell differentiation and apoptosis are accompanied with changes of biophysical properties of cell membranes, and by modulation of constitution, structure, symmetry and metabolism of cell lipids. Suggesting differences of these events in normal and tumor cells we compared the response of human colonic cell lines derived from normal fetal tissue (FHC) and colon adenocarcinoma (HT-29, HCT116) to treatment with sodium butyrate (NaBt, 3 mM) and PUFAs (50 microM) of n-6 (arachidonic acid, AA) or n-3 (docosahexaenoic acid, DHA) series and their combination. Using flow cytometry as the main methodology we detected modulations of proliferation, differentiation (activity of alkaline phosphatase), and cell death (% of floating cells, nuclear morphology). FHC cells were more sensitive to NaBt, PUFAs and especially to theircombination than cancer cells. Induction of FHC cell apoptosis was associated with decrease omitochondrial membrane potential (MMP- TMRE), membrane lipid unpacking (MC540), acumulation of lipid droplets (NILE RED). The role of oxidative stress (detection of ROS, DHR-123) and caspases was verified by using appropriate antioxidants (NAC, TROLOX) and caspase inhibitor Z-VAD. Content and composition of phospholipids and fatty acids (LC/MS, GC/MS) after treatment of agents studied differed in normal and cancer cells. Detection of these alterations and their correlation with other parameters reflecting differentiation and apoptosis contribute to clarifying of sequencing and regulation of particular steps of these processes and differences between normal and cancer cells. This work was supported by grants No. 524/07/1178 GACR, 301/07/1557 GACR, 1QS500040507 IGA ASCR