In vitro senescence enhances IL-6 production in human gingival fibroblasts induced by lipopolysaccharide from Campylobacter rectus

Mech Ageing Dev. 1996 May 24;87(1):47-59. doi: 10.1016/0047-6374(96)01701-0.

Abstract

The production of interleukin-6 (IL-6) in human gingival fibroblasts (Gin cells) is increased by lipopolysaccharide (LPS) from Campylobacter rectus (C. rectus), which is associated with adult periodontitis; however, the age-related changes in the susceptibility of Gin cells to C. rectus LPS remain unclear. We examined the influence of in vitro senescence on C. rectus LPS-stimulated IL-6 production in Gin cells. LPS was prepared from C. rectus ATCC 33238 using hot phenol-water. The Gin cells were established from healthy gingival tissue removed from three patients, aged 10-12 years. The cells were cultured until confluence then stimulated with LPS (0.01, 0.1, 1.0 and 10.0 micrograms/ml). Levels of IL-6 released in the medium were measured after incubation for 3, 6, 9, 12, and 24 h. In both young (5-6 population doublings) and senescent (17-20 population doublings) cells, LPS stimulated IL-6 production in a dose- and time-dependent manner. In response to 0.01-10.0 micrograms/ml of LPS, IL-6 production in the senescent cells was higher than that in the young cells. Using cells from each of the three donors, we found that this phenomenon of higher LPS-stimulated IL-6 production in senescent cells was reproducible. The greater capacity of the senescent cells to synthesize IL-6 in response to LPS was a higher production of mRNA for IL-6. This increase of IL-6 production induced by C. rectus LPS in senescent Gin cells could help to explain the increased susceptibility to periodontal diseases shown by aged individuals.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Base Sequence
  • Campylobacter / pathogenicity
  • Cellular Senescence / immunology*
  • Child
  • Fibroblasts / cytology
  • Fibroblasts / immunology
  • Gene Expression
  • Gingiva / cytology
  • Gingiva / immunology*
  • Humans
  • In Vitro Techniques
  • Interleukin-6 / biosynthesis*
  • Interleukin-6 / genetics
  • Lipopolysaccharides / isolation & purification
  • Lipopolysaccharides / pharmacology
  • Periodontitis / etiology
  • RNA, Messenger / genetics

Substances

  • Interleukin-6
  • Lipopolysaccharides
  • RNA, Messenger