4.5 Article

Calcium Hydroxide Inactivates Lipoteichoic Acid from Enterococcus faecalis through Deacylation of the Lipid Moiety

Journal

JOURNAL OF ENDODONTICS
Volume 37, Issue 2, Pages 191-196

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.joen.2010.11.007

Keywords

Apical periodontitis; calcium hydroxide; Enterococcus faecalis; intracanal medicament; lipoteichoic acid; matrix-assisted laser desorption ionization time of flight

Funding

  1. Korean Government [KRF-2008-314-E00223]
  2. Korea government (MEST) [2010-0029116]
  3. Korean Ministry of Education, Science and Technology, Republic of Korea [20100001746]
  4. National Research Foundation of Korea [2008-0062421, 2006-2008395, 과09A1215] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Introduction: Lipoteichoic acid (LTA) is a major virulence factor of Enterococcus faecal is that is closely associated with refractory apical periodontitis. Recently, we have shown that calcium hydroxide, a commonly used intracanal medicament, abrogated the ability of LTA to stimulate the production of tumor necrosis factor alpha in a murine macrophage line, RAW 264.7. Because calcium hydroxide could potentially modify the glycolipid moiety of LTA, we examined if calcium hydroxide inactivates LTA through deacylation of the LTA. Methods: LTA was prepared from E. faecalis by organic solvent extraction followed by chromatography with the hydrophobic-interaction column and the ion-exchange column. RAW 264.7 cells were stimulated with intact LTA or calcium hydroxide treated LTA for 24 hours, and the productions of nitric oxide (NO) and chemokines interferon-gamma induced protein (IP-10) and macrophage inflammatory protein-1 alpha (MIP-1 alpha) were determined. The glycolipid structure of LTA was analyzed using matrix-assisted laser desorption ionization-time of flight mass spectrometry and thin layer chromatography (TLC). Results: The production of NO, IP-1, and MIP-1 alpha was augmented in LTA-stimulated cells, whereas no such effect was observed upon stimulation with calcium hydroxide pretreated LTA. Mass spectrometry showed that intact glycolipids of LTA yielded distinct mass peaks at 930 to 1,070 mass over charge (m/z) units, corresponding to dihexosyl-diacylglycerol consisting of two acyl chains with chain lengths of C-16 to C-22 and with one or two unsaturated double bonds. However, those peaks were not observed in the mass spectra of the calcium hydroxide-treated LTA. Furthermore, free fatty acids released from the calcium hydroxide-treated LTA were detected using TLC. Conclusion: We suggest that calcium hydroxide attenuates the inflammatory activity of E. faecal is LTA through deacylation of the LTA. (J Endod 2011;37:191-196)

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