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PMID: 10024594 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

In vitro induction of activation-induced cell death in lymphocytes from chronic periodontal lesions by exogenous Fas ligand.

Infection and immunity ·Vol. 67 ·No. 3 ·1999-03-00 ·Pages 1450-4

Sawa T, Nishimura F, Ohyama H, Takahashi K, Takashiba S, Murayama Y

Abstract

Periodontitis is a chronic inflammatory disease which gradually destroys the supporting tissues of the teeth, leading to tooth loss in adults. The lesions are characterized by a persistence of inflammatory cells in gingival and periodontal connective tissues. To understand what mechanisms are involved in the establishment of chronic lesions, we hypothesized that infiltrating lymphocytes might be resistant to apoptosis. However, both Bcl-2 and Bcl-xL were weakly detected in lymphocytes from the lesions, compared with those from peripheral blood, suggesting that these cells are susceptible to apoptosis. Nevertheless, very few apoptotic cells were observed in tissue sections from the lesions. Lymphocytes from the lesions expressed mRNA encoding Fas, whereas Fas-ligand mRNA was very weakly expressed in lymphocytes from the lesions and in periodontal tissues. Since the results indicated that lymphocytes in the lesions might be susceptible to Fas-mediated apoptosis but lack the death signal, we next investigated if these lymphocytes actually undergo apoptosis by the addition of anti-Fas antibodies in vitro. Fas-positive lymphocytes from the lesions underwent apoptosis by these antibodies, but Fas-negative lymphocytes and Fas-positive peripheral lymphocytes did not undergo apoptosis by these antibodies. These results indicate that lymphocytes in the lesions are susceptible to activation-induced cell death and are induced to die by apoptosis after the addition of exogenous Fas ligand.

MeSH Terms
Adult Apoptosis/drug effects Chronic Disease Fas Ligand Protein Humans Lymphocyte Activation Lymphocytes/pathology Membrane Glycoproteins/genetics,pharmacology Periodontal Diseases/pathology Proto-Oncogene Proteins c-bcl-2/analysis RNA, Messenger/analysis bcl-X Protein fas Receptor/genetics
Chemicals
BCL2L1 protein, human FASLG protein, human Fas Ligand Protein Membrane Glycoproteins Proto-Oncogene Proteins c-bcl-2 RNA, Messenger bcl-X Protein fas Receptor
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Sawa T
Department of Periodontology and Endodontology, Okayama University Dental School, Okayama, Japan.
Nishimura F
Ohyama H
Takahashi K
Takashiba S
Murayama Y
References (20)
20 references, click to expand
  1. Demonstration of mycobacterial antigens in nerve biopsies from leprosy patients using peroxidase-antiperoxidase immunoenzyme technique.
    Clin Immunol Immunopathol. 1983 Dec;29(3):359-68 PMID: 6416726
  2. Absence of exogenous interleukin-4-induced apoptosis of gingival macrophages may contribute to chronic inflammation in periodontal diseases.
    Am J Pathol. 1996 Jan;148(1):331-9 PMID: 8546223
  3. Suppressor T lymphocytes from lepromatous leprosy skin lesions.
    J Immunol. 1986 Nov 1;137(9):2831-4 PMID: 2944966
  4. In situ locations of Mycobacterium leprae-specific antigens. Immunoelectronoptical studies.
    Acta Leprol. 1989;7 Suppl 1:107-12 PMID: 2503963
  5. Serum immunoglobulin G antibody to periodontal bacteria.
    Adv Dent Res. 1988 Nov;2(2):339-45 PMID: 3271028
  6. Cellular analysis of functional mononuclear cells from chronically inflamed gingival tissue.
    Reg Immunol. 1989 Mar-Apr;2(2):103-10 PMID: 2701813
  7. Identification of programmed cell death in situ via specific labeling of nuclear DNA fragmentation.
    J Cell Biol. 1992 Nov;119(3):493-501 PMID: 1400587
  8. Immunohistological analysis of memory T lymphocytes and activated B lymphocytes in tissues with periodontal disease.
    J Periodontal Res. 1993 Sep;28(5):324-34 PMID: 7692033
  9. Immunoblot analysis of cellular expression of Bcl-2 family proteins, Bcl-2, Bax, Bcl-X and Mcl-1, in human peripheral blood and lymphoid tissues.
    Int Immunol. 1995 Nov;7(11):1817-25 PMID: 8580080
  10. Therapeutic effect of the anti-Fas antibody on arthritis in HTLV-1 tax transgenic mice.
    J Clin Invest. 1996 Jul 15;98(2):271-8 PMID: 8755634
  11. Induction of Fas-dependent apoptosis in synovial infiltrating cells in rheumatoid arthritis.
    Int Immunol. 1996 Oct;8(10):1595-602 PMID: 8921439
  12. Apoptosis by death factor.
    Cell. 1997 Feb 7;88(3):355-65 PMID: 9039262
  13. The nature of periodontal diseases.
    Ann Periodontol. 1997 Mar;2(1):3-10 PMID: 9151538
  14. The proto-oncogene Bcl-2 and its role in regulating apoptosis.
    Nat Med. 1997 Jun;3(6):614-20 PMID: 9176486
  15. Adult periodontitis--specific bacterial infection or chronic inflammation?
    J Med Microbiol. 1998 Mar;47(3):187-8 PMID: 9511822
  16. Homeostasis and self-tolerance in the immune system: turning lymphocytes off.
    Science. 1998 Apr 10;280(5361):243-8 PMID: 9535647
  17. Deletions of the cyclin-dependent kinase-4 inhibitor gene in multiple human cancers.
    Nature. 1994 Apr 21;368(6473):753-6 PMID: 8152487
  18. Cloning, characterization, and antigen specificity of T-lymphocyte subsets extracted from gingival tissue of chronic adult periodontitis patients.
    Infect Immun. 1995 Jun;63(6):2147-53 PMID: 7539406
  19. Expression of Fas/APO-1 during the progression of astrocytomas.
    Cancer Res. 1995 Dec 1;55(23):5528-30 PMID: 7585627
  20. Phenotypic studies of cells from periodontal disease tissues.
    J Periodontal Res. 1984 Nov;19(6):587-90 PMID: 6241232
Article Info
Journal
Infection and immunity
Abbr.
Infect Immun
ISSN
0019-9567
Published
1999-03-00
Pages
1450-4
Language
English
Region
United States
NLM ID
0246127
PMCID
PMC96480
Subset
IM
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