Premium
Butyrate, a bacterial metabolite, induces apoptosis and autophagic cell death in gingival epithelial cells
Author(s) -
Tsuda H.,
Ochiai K.,
Suzuki N.,
Otsuka K.
Publication year - 2010
Publication title -
journal of periodontal research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.31
H-Index - 83
eISSN - 1600-0765
pISSN - 0022-3484
DOI - 10.1111/j.1600-0765.2010.01277.x
Subject(s) - programmed cell death , butyrate , apoptosis , phosphatidylserine , annexin , microbiology and biotechnology , biology , caspase , annexin a5 , viability assay , chemistry , biochemistry , phospholipid , membrane , fermentation
Tsuda H, Ochiai K, Suzuki N, Otsuka K. Butyrate, a bacterial metabolite, induces apoptosis and autophagic cell death in gingival epithelial cells. J Periodont Res 2010; 45: 626–634. © 2010 John Wiley & Sons A/S Background and Objective: Butyrate is produced by some types of anaerobic periodontal bacteria. Millimolar concentrations of butyrate are found in mature dental plaque from periodontitis patients. Although butyrate reportedly has a variety of effects in many mammalian cells, its effect on gingival epithelial cells is not well known. In this study, we investigated the effect of butyrate on gingival epithelial Ca9‐22 cell death. Material and Methods: Death of Ca9‐22 cells was assessed after treating the cells with or without butyrate. A SYTOX Green dye, which exhibits strong green fluorescence once it enters dead cells through ruptured cell membranes, was used for cell death detection. Phosphatidylserine redistribution was measured using fluorescein isothiocyanate‐labeled annexin V. The activity of caspase‐3 was measured as the amount of cleaved substrate peptide. Anti‐apoptotic bcl‐2 mRNA expression was measured using real‐time RT‐PCR. Western blotting and fluoromicroscopic analysis with anti‐microtubule‐associated protein 1 light chain 3 (LC3) antibodies were performed for detection of autophagy. Results: Stimulation with millimolar concentrations of butyrate for 48 h induced Ca9‐22 cell death. The stimulation also caused increased caspase‐3 activity, phosphatidylserine redistribution and bcl‐2 down‐regulation, suggesting butyrate‐induced apoptosis. However, the pan‐caspase inhibitor, Z‐VAD‐FMK, did not inhibit cell death completely. This implies the existence of other types of cell death. In addition, markers of autophagy, namely, the conversion of LC3‐I to LC3‐II and increased LC3 accumulation, were observed. Moreover, inhibition of autophagy by 3‐methyladenine suppressed the butyrate‐induced cell death, suggesting that butyrate could induce cell death through autophagy. Conclusion: These data suggest that butyrate induces apoptosis and autophagic cell death.