Papers

Peer-reviewed International journal
Mar, 1999

In Vitro Induction of Activation-Induced Cell Death in Lymphocytes from Chronic Periodontal Lesions by Exogenous Fas Ligand

Infection and Immunity
  • Takamasa Sawa
  • ,
  • Fusanori Nishimura
  • ,
  • Hideki Ohyama
  • ,
  • Keiso Takahashi
  • ,
  • Shogo Takashiba
  • ,
  • Yoji Murayama

Volume
67
Number
3
First page
1450
Last page
1454
Language
English
Publishing type
Research paper (scientific journal)
DOI
10.1128/iai.67.3.1450-1454.1999
Publisher
American Society for Microbiology

<title>ABSTRACT</title>
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.

Link information
DOI
https://doi.org/10.1128/iai.67.3.1450-1454.1999
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/10024594
PubMed Central
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC96480
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000078736300058&DestApp=WOS_CPL
URL
https://journals.asm.org/doi/pdf/10.1128/IAI.67.3.1450-1454.1999
ID information
  • DOI : 10.1128/iai.67.3.1450-1454.1999
  • ISSN : 0019-9567
  • eISSN : 1098-5522
  • ORCID - Put Code : 47542654
  • Pubmed ID : 10024594
  • Pubmed Central ID : PMC96480
  • Web of Science ID : WOS:000078736300058

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