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Regulation of matrix metalloproteinase-9 expression between gingival fibroblast cells from old and young rats

Authors
Kim, SJ[Kim, Su-Jung]Chung, YK[Chung, Yong-Koo]Chung, TW[Chung, Tae-Wook]Kim, JR[Kim, Jeong-Ran]Moon, SK[Moon, Sung-Kwon]Kim, CH[Kim, Cheorl-Ho]Park, YG[Park, Young-Guk]
Issue Date
9-Jan-2009
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
Keywords
Aging; Proliferative capacity; G1 cell cycle; MMP-9; Gingival fibroblasts
Citation
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.378, no.2, pp.152 - 156
Indexed
SCIE
SCOPUS
Journal Title
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
Volume
378
Number
2
Start Page
152
End Page
156
URI
https://scholarworks.bwise.kr/skku/handle/2021.sw.skku/78667
DOI
10.1016/j.bbrc.2008.09.015
ISSN
0006-291X
Abstract
Gingival fibroblast cells (rGF) from aged rats have an age-related decline in proliferative capacity compared with young rats. We investigated G1 phase cell cycle regulation and MMP-9 expression in both young and aged rGF. G1 cell cycle protein levels and activity were significantly reduced in response to interleukin-1 beta (IL-1 beta) stimulation with increasing in vitro age. Tumor necrosis factor-alpha (TNF-alpha)-induced matrix metalloproteinase-9 (MMP-9) expression was also decreased in aged rGF in comparison with young rGF. Mutational analysis and gel shift assays demonstrated that the lower MMP-9 expression ill aged rGF is associated with lower activities of transcription factors NF-kappa B and AP-1. These results Suggest that cell cycle dysregulation and down-regulation of MMP-9 expression in rGF may play a role in gingival remodeling during in vitro aging. (C) 2008 Published by Elsevier Inc.
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