Influence of Aging on Biological Properties of Periodontal Ligament Cells

被引:35
作者
Benatti, Bruno Braga [1 ]
Silverio, Karina Gonzales [2 ]
Casati, Marcio Zaffalon [2 ]
Sallum, Enilson Antonio [2 ]
Nociti, Francisco Humberto, Jr. [2 ]
机构
[1] Maranhao Univ Ctr, Dept Hlth Sci, Sao Luis, Maranhao, Brazil
[2] Univ Estadual Campinas, Sch Dent, Div Periodont, Dept Prosthodont & Periodont, Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
Aging; Periodontal Ligament; Cells; Gene Expression; Periodontal Heaing;
D O I
10.1080/03008200802171159
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
The majority of patients eligible for periodontal regenerative therapies are aged subjects. Since periodontal ligament cells (PDLC) are essential for periodontal regeneration, the aim of the present study was to determine the effect of cellular aging on PDLC, including genes associated with extracellular matrix metabolism and growth-associated factors. PDLC cultures were obtained from subjects aged. 15 to 20 years and subjects aged more than 60 years. Proliferation; cell viability, mineralization assays, and mRNA levels were assessed for type I and III collagen, platelet-derived growth factor (PDGF)-1, basic fibroblast growth factor (bFGF), metalloproteinase (MMP)-2 and -8, and tissue inhibitor of metalloproteinases (TIMP)-1 and -2. Data analysis demonstrated that aging negatively influenced cell proliferation and mineral nodule formation (p < 0.05). Gene expression analysis further showed that mRNA levels for bFGF, PDGF-1, and TIMP-2 were not affected by aging (p > 0.05). In addition, mRNA levels for type I and fit collagen were significantly lower in aged cells (p < 0.05), whereas MMP-2 and -8 and TIMP-I mRNA levels were higher (p < 0.05). Within the limits of the present study, data analysis suggests that aging-modulates important biological properties of periodontal ligament cells; diminishes the potential for mineral nodule formation, and favors extracellular matrix degradation.
引用
收藏
页码:401 / 408
页数:8
相关论文
共 51 条
[1]
Abiko Y, 1998, Ann Periodontol, V3, P350
[2]
AINAMO J, 1975, INT DENT J, V25, P229
[3]
KINETICS OF I-125 PDGF BINDING AND DOWN-REGULATION OF PDGF RECEPTOR IN HUMAN ARTERIAL SMOOTH-MUSCLE CELL STRAINS DURING CELLULAR SENESCENCE IN-VITRO [J].
AOYAGI, M ;
FUKAI, N ;
OGAMI, K ;
YAMAMOTO, M ;
YAMAMOTO, K .
JOURNAL OF CELLULAR PHYSIOLOGY, 1995, 164 (02) :376-384
[4]
HUMAN PERIODONTAL CELLS INITIATE MINERAL-LIKE NODULES INVITRO [J].
ARCEO, N ;
SAUK, JJ ;
MOEHRING, J ;
FOSTER, RA ;
SOMERMAN, MJ .
JOURNAL OF PERIODONTOLOGY, 1991, 62 (08) :499-503
[5]
Age-related changes in gene expression patterns of matrix metalloproteinases and their collagenous substrates in mandibular condylar cartilage in rats [J].
Bae, JW ;
Takahashi, I ;
Sasano, Y ;
Onodera, K ;
Mitani, H ;
Kagayama, M ;
Mitani, H .
JOURNAL OF ANATOMY, 2003, 203 (02) :235-241
[6]
Bancroft J. D., 1990, THEORY PRACTICE HIST
[7]
BARLOLD PM, 2000, PERIODONTOL, V24, P253
[8]
Osteoblast-like properties of human periodontal ligament cells: an in vitro analysis [J].
Basdra, EK ;
Komposch, G .
EUROPEAN JOURNAL OF ORTHODONTICS, 1997, 19 (06) :615-621
[9]
Periodontal healing may be affected by aging: a histologic study in rats [J].
Benatti, B. B. ;
Neto, J. B. C. ;
Casati, M. Z. ;
Sallum, E. A. ;
Sallum, A. W. ;
Nociti, F. H., Jr. .
JOURNAL OF PERIODONTAL RESEARCH, 2006, 41 (04) :329-333
[10]
MATRIX METALLOPROTEINASES - A REVIEW [J].
BIRKEDALHANSEN, H ;
MOORE, WGI ;
BODDEN, MK ;
WINDSOR, LJ ;
BIRKEDALHANSEN, B ;
DECARLO, A ;
ENGLER, JA .
CRITICAL REVIEWS IN ORAL BIOLOGY & MEDICINE, 1993, 4 (02) :197-250