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Infect Immun, June 1998, p. 2587-2594, Vol. 66, No. 6
Department of Microbiology, Nihon University
School of Dentistry at Matsudo, Matsudo, Chiba 271, Japan
Received 18 November 1997/Returned for modification 5 February
1998/Accepted 16 March 1998
The ability of butyric acid, an extracellular metabolite from
periodontopathic bacteria, to induce apoptosis in murine WEHI 231 cells, splenic B cells, and human RAJI cells was examined. The culture
filtrate of Porphyromonas gingivalis,
Prevotella loescheii, and Fusobacterium
nucleatum, which contains high a percentage of butyric
acid, induced DNA fragmentation in WEHI 231 cells. Volatile fatty acid,
especially butyric acid, significantly suppressed B-cell viability in a
concentration-dependent fashion. The DNA fragmentation assay indicated
that butyric acid rapidly induced apoptosis in WEHI 231 cells (with
1.25 mM butyric acid and 6 h after treatment), splenic B cells
(with 1.25 mM butyric acid), and RAJI cells (with 2.5 mM butyric acid).
Incubation of WEHI 231 cells with butyric acid for 16 h resulted
in the typical ladder pattern of DNA fragmentation and the
apoptoic change such as chromatin condensation and hypodiploid
nuclei. Cell cycle analysis implied that butyric acid arrested the
cells at the G1 phase. The inhibitory assay suggested that
butyric acid-induced apoptosis of WEHI 231 and splenic B cells
was inhibited by W-7, a calmodulin inhibitor. These results suggest
that calmodulin-dependent regulation is involved in the signal
transduction pathway of butyric acid.
0019-9567/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Volatile Fatty Acid, Metabolic By-Product of
Periodontopathic Bacteria, Induces Apoptosis in WEHI 231 and RAJI B
Lymphoma Cells and Splenic B Cells
*
Corresponding author. Mailing address: Department of
Microbiology, Nihon University School of Dentistry at Matsudo,
Matsudo-shi, Chiba 271, Japan. Phone: 473-68-6111. Fax:
473-64-6295. E-mail: tkurita{at}mascat.nihon-u.ac.jp.
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