Literature DB >> 10505799

Age-dependent changes in the distribution of BrdU- and TUNEL-positive cells in the murine gingival tissue.

T Sakai1, T Kiyoshima, I Kobayashi, R Moroi, T Ibuki, M Nagadome, Y Terada, H Sakai.   

Abstract

BACKGROUND: Age-dependent morphological and cell kinetic changes of the gingival tissue seem to be related to the occurrence of periodontal disease. The purpose of this study was to investigate the age-dependent changes in the distribution of BrdU- and TUNEL-positive cells in murine gingival tissue.
METHODS: Gingival tissue of the lower first molar region of 2-, 3-, 5-, 7-, 10-, 15-, 20-, 30-, 40-, 50-, 60-, 70- and 80-week-old mice was used in this study. BrdU- and TUNEL-positive cells were evaluated at the following 4 sites: 1) gingival epithelium (GE); 2) junctional epithelium (JE); 3) submucosal connective tissue of the gingival epithelium (GECT); and 4) submucosal connective tissue of the junctional epithelium (JECT).
RESULTS: No significant differences in the mean number of BrdU-positive cells at each site were demonstrated among the various age groups. No significant change in the mean number of TUNEL-positive cells was demonstrated in either the GE or JE groups among the various age groups. Meanwhile, a significant increase in the TUNEL-positive cells was observed in the GECT of mice 40 weeks or older, and in the JECT of mice 20 weeks or older.
CONCLUSIONS: These results indicate that no age-dependent change in the cell proliferation or cell death occurred in the gingival and junctional epithelial layers as well as in the cell proliferation in the submucosal connective tissue. Meanwhile, a significant decrease in the cellular component of the submucosal connective tissue of both gingival and junctional epithelial layers caused by apoptosis occurred with aging. The decreased cellular component in the submucosal connective tissue thus seems to be related to either gingival recession or to the apical migration of the JE with aging. These morphological changes with aging possibly occur in humans and may be related to the susceptibility to periodontal disease in aged individuals.

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Year:  1999        PMID: 10505799     DOI: 10.1902/jop.1999.70.9.973

Source DB:  PubMed          Journal:  J Periodontol        ISSN: 0022-3492            Impact factor:   6.993


  4 in total

1.  Age-dependent changes in cell proliferation and cell death in the periodontal tissue and the submandibular gland in mice: a comparison with other tissues and organs.

Authors:  Norio Enoki; Tamotsu Kiyoshima; Takako Sakai; Ieyoshi Kobayashi; Keiko Takahashi; Yoshihiro Terada; Hidetaka Sakai
Journal:  J Mol Histol       Date:  2007-06-20       Impact factor: 2.611

2.  Localization of heat shock protein 27 (hsp27) in the rat gingiva and its changes with tooth eruption.

Authors:  Au Sasaki; Tohru Yamada; Katsuyuki Inoue; Tomoko Momoi; Hiroshi Tokunaga; Koji Sakiyama; Haruhide Kanegae; Naoto Suda; Osamu Amano
Journal:  Acta Histochem Cytochem       Date:  2011-02-23       Impact factor: 1.938

3.  The junctional epithelium originates from the odontogenic epithelium of an erupted tooth.

Authors:  Sara Yajima-Himuro; Masamitsu Oshima; Gou Yamamoto; Miho Ogawa; Madoka Furuya; Junichi Tanaka; Kousuke Nishii; Kenji Mishima; Tetsuhiko Tachikawa; Takashi Tsuji; Matsuo Yamamoto
Journal:  Sci Rep       Date:  2014-05-02       Impact factor: 4.379

4.  Oxidative stress caused by a low concentration of hydrogen peroxide induces senescence-like changes in mouse gingival fibroblasts.

Authors:  Tamotsu Kiyoshima; Norio Enoki; Ieyoshi Kobayashi; Takako Sakai; Kengo Nagata; Hiroko Wada; Hiroaki Fujiwara; Yukiko Ookuma; Hidetaka Sakai
Journal:  Int J Mol Med       Date:  2012-08-20       Impact factor: 4.101

  4 in total

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