The antimicrobial peptide LL-37 is anti-inflammatory and proapoptotic in human periodontal ligament cells
Article first published online: 9 NOV 2011
© 2011 John Wiley & Sons A/S
Journal of Periodontal Research
Volume 47, Issue 3, pages 330–335, June 2012
How to Cite
Jönsson, D. and Nilsson, B.-O. (2012), The antimicrobial peptide LL-37 is anti-inflammatory and proapoptotic in human periodontal ligament cells. Journal of Periodontal Research, 47: 330–335. doi: 10.1111/j.1600-0765.2011.01436.x
- Issue published online: 19 APR 2012
- Article first published online: 9 NOV 2011
- Accepted for publication October 10, 2011
- DNA synthesis;
- monocyte chemoattractant protein-1;
- periodontal ligament cell
Jönsson D, Nilsson B-O. The antimicrobial peptide LL-37 is anti-inflammatory and proapoptotic in human periodontal ligament cells. J Periodont Res 2012; 47: 330–335. © 2011 John Wiley & Sons A/S
Background and Objective: The antimicrobial peptide LL-37 is expressed in periodontal tissue, and variations in LL-37 levels have been associated with periodontal disease. The effects of LL-37 on periodontal ligament cell function have not been described before. Here, we assess anti-inflammatory properties of LL-37 and investigate the effects of LL-37 on cell differentiation, cell proliferation and apoptosis in human periodontal ligament cells.
Material and Methods: Periodontal ligament cells were obtained from teeth extracted for orthodontic reasons. Cytokine (interleukin-6) and chemokine (monocyte chemoattractant protein-1) expression was determined by quantitative PCR, cell differentiation by alkaline phosphatase activity, cell proliferation by counting cells in a Bürker chamber, DNA synthesis by incorporation of radiolabeled thymidine and apoptosis by cell morphology and activated caspase 3 quantities.
Results: Treatment with 0.1 and 1 μm of LL-37 totally reversed lipopolysaccharide-induced monocyte chemoattractant protein-1 expression and suppressed lipopolysaccharide-induced interleukin-6 expression by 50–70%. LL-37 had no effect on alkaline phosphatase activity. Incubation with 8 μm LL-37 strongly reduced cell number. DNA synthesis was attenuated by about 90% in response to 8 μm LL-37, confirming its antiproliferative effect. Cell morphology was altered in an apoptosis-like fashion in cells treated with 8 μm LL-37. Furthermore, the quantity of activated caspase 3 was increased in cells treated with 1 and 8 μm of LL-37, suggesting apoptosis.
Conclusion: LL-37 strongly attenuates lipopolysaccharide-induced cytokine and chemokine expression and, in high concentrations, reduces cell proliferation through inhibition of DNA synthesis and by promoting apoptosis in human periodontal ligament cells.