Are cementoblasts a subpopulation of osteoblasts or a unique phenotype?

被引:293
作者
Bosshardt, DD [1 ]
机构
[1] Univ Bern, Sch Dent Med, Dept Periodontol & Fixed Prosthodont, CH-3010 Bern, Switzerland
关键词
cementoblast; osteoblast; periodontal regeneration; periodontal ligament; cementum; bone; enamel matrix proteins;
D O I
10.1177/154405910508400501
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Experimental studies have shown a great potential for periodontal regeneration. The limitations of periodontal regeneration largely depend on the regenerative potential at the root surface. Cellular intrinsic fiber cementum (CIFC), so-called bone-like tissue, may form instead of the desired acellular extrinsic fiber cementum (AEFC), and the interfacial tissue bonding may be weak. The periodontal ligament harbors progenitor cells that can differentiate into periodontal ligament fibroblasts, osteoblasts, and cementoblasts, but their precise location is unknown. It is also not known whether osteoblasts and cementoblasts arise from a common precursor cell line, or whether distinct precursor cell lines exist. Thus, there is limited knowledge about how cell diversity evolves in the space between the developing root and the alveolar bone. This review supports the hypothesis that AEFC is a unique tissue, while CIFC and bone share some similarities. Morphologically, functionally, and biochemically, however, CIFC is distinctly different from any bone type. There are several lines of evidence to propose that cementoblasts that produce both AEFC and CIFC are unique phenotypes that are unrelated to osteoblasts. Cementum attachment protein appears to be cementum-specific, and the expression of two proteoglycans, fibromodulin and lumican, appears to be stronger in CIFC than in bone. A theory is presented that may help explain how cell diversity evolves in the periodontal ligament. It proposes that Hertwig's epithelial root sheath and cells derived from it play an essential role in the development and maintenance of the periodontium. The role of enamel matrix proteins in cementoblast and osteoblast differentiation and their potential use for tissue engineering are discussed.
引用
收藏
页码:390 / 406
页数:17
相关论文
共 259 条
[71]   Effect of porcine fetal enamel matrix derivative on chondrocyte proliferation, differentiation, and local factor production is dependent on cell maturation state [J].
Dean, DD ;
Lohmann, CH ;
Sylvia, VL ;
Cochran, DL ;
Liu, Y ;
Boyan, BD ;
Schwartz, Z .
CELLS TISSUES ORGANS, 2002, 171 (2-3) :117-127
[72]   Expression of bone associated markers by tooth root lining cells, in situ and in vitro [J].
DErrico, JA ;
Macneil, RL ;
Takata, T ;
Berry, J ;
Strayhorn, C ;
Somerman, MJ .
BONE, 1997, 20 (02) :117-126
[73]   Early bone healing events in the human extraction socket [J].
Devlin, H ;
Sloan, P .
INTERNATIONAL JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY, 2002, 31 (06) :641-645
[74]   Wound healing of degree III furcation involvements following guided tissue regeneration and/or Emdogain® -: A histologic study [J].
Donos, N ;
Sculean, A ;
Glavind, L ;
Reich, E ;
Karring, T .
JOURNAL OF CLINICAL PERIODONTOLOGY, 2003, 30 (12) :1061-1068
[75]   Gene expression patterns of murine dentin matrix protein 1 (Dmp1) and dentin sialophosphoprotein (DSPP) suggest distinct developmental functions in vivo [J].
DSouza, RN ;
Cavender, A ;
Sunavala, G ;
Alvarez, J ;
Ohshima, T ;
Kulkarni, AB ;
MacDougall, M .
JOURNAL OF BONE AND MINERAL RESEARCH, 1997, 12 (12) :2040-2049
[76]  
Ducy P, 2000, DEV DYNAM, V219, P461, DOI 10.1002/1097-0177(2000)9999:9999<::AID-DVDY1074>3.0.CO
[77]  
2-C
[78]  
ELLABBAN NG, 1990, J ORAL PATHOL MED, V19, P166
[79]   Proteoglycans in dentinogenesis [J].
Embery, G ;
Hall, R ;
Waddington, R ;
Septier, D ;
Goldberg, M .
CRITICAL REVIEWS IN ORAL BIOLOGY & MEDICINE, 2001, 12 (04) :331-349
[80]   The dentin matrix protein 1 (Dmp1) is specifically expressed in mineralized, but not soft, tissues during development [J].
Feng, JQ ;
Huang, H ;
Lu, Y ;
Ye, L ;
Xie, Y ;
Tsutsui, TW ;
Kunieda, T ;
Castranio, T ;
Scott, G ;
Bonewald, LB ;
Mishina, Y .
JOURNAL OF DENTAL RESEARCH, 2003, 82 (10) :776-780