Review: Extracellular matrix regulates tooth morphogenesis

被引:59
作者
Fukumoto, S
Yamada, Y
机构
[1] Kyushu Univ, Fac Dent Sci, Div Oral Hlth Growth & Dev, Sect Pediat Dent,Higashi Ku, Fukuoka 8128582, Japan
[2] Natl Inst Dent & Craniofacial Res, Craniofacial Dev Biol & Regenerat Branch, NIH, Bethesda, MD USA
关键词
extracellular matrix; basement membrane; tooth; enamel; dentin;
D O I
10.1080/03008200500344017
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mineralized tissues are unique in that they use proteins to attract and organize calcium and phosphate ions into a structured mineral phase, thus precise knowledge of the expression and extracellular distribution of matrix proteins is very important to understand their function. Tooth development is regulated by sequential and reciprocal interactions between neural crest-derived mesenchymal cells and the oral environment. However, the precise molecular mechanisms that mediate interactions between epithelium and mesenchymal cells are not clear, although basement membrane (BM) components have been shown to play important roles in these regulatory events. In addition, the extracellular matrix layer, whose main components are laminin, collagen IV, nidogen, and sulfated proteoglycan, and the BM layer are both considered to be involved with cell proliferation and differentiation. During tooth morphogenesis, extracellular matrices are dramatically changed. Further, the BM components, laminin and collagen IV support dental epithelium; however, in the late stage, they begin the processes of enamel matrix secretion and calcification, after which the BM structure between the dental epithelium and mesenchyme disappears. In addition, tooth abnormalities associated with several kinds of human diseases that cause mutations in the extracellular matrix, as well as the molecular mechanisms of the basement membrane and enamel matrix during tooth morphogenesis, are not clearly understood. In our review, we discuss the role of the extracellular matrix, with focus on the BM and enamel matrix during tooth morphogenesis.
引用
收藏
页码:220 / 226
页数:7
相关论文
共 55 条
[11]   The structural biology of the developing dental enamel matrix [J].
Fincham, AG ;
Moradian-Oldak, J ;
Simmer, JP .
JOURNAL OF STRUCTURAL BIOLOGY, 1999, 126 (03) :270-299
[12]  
Fong CD, 1996, J BONE MINER RES, V11, P892
[13]   Ameloblastin is a cell adhesion molecule required for maintaining the differentiation state of ameloblasts [J].
Fukumoto, S ;
Kiba, T ;
Hall, B ;
Iehara, N ;
Nakamura, T ;
Longenecker, G ;
Krebsbach, PH ;
Nanci, A ;
Kulkarni, AB ;
Yamada, Y .
JOURNAL OF CELL BIOLOGY, 2004, 167 (05) :973-983
[14]   Amelogenin-deficient mice display an amelogenesis imperfecta phenotype [J].
Gibson, CW ;
Yuan, ZA ;
Hall, B ;
Longenecker, G ;
Chen, EH ;
Thyagarajan, T ;
Sreenath, T ;
Wright, JT ;
Decker, S ;
Piddington, R ;
Harrison, G ;
Kulkarni, AB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (34) :31871-31875
[15]   Processing of laminin-5 and its functional consequences: Role of plasmin and tissue-type plasminogen activator [J].
Goldfinger, LE ;
Stack, MS ;
Jones, JCR .
JOURNAL OF CELL BIOLOGY, 1998, 141 (01) :255-265
[16]   The receptor activator of nuclear factor-B ligand-mediated osteoclastogenic pathway is elevated in amelogenin-null mice [J].
Hatakeyama, J ;
Sreenath, T ;
Hatakeyama, Y ;
Thyagarajan, T ;
Shum, L ;
Gibson, CW ;
Wright, JT ;
Kulkarni, AB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (37) :35743-35748
[17]   Murine Enamelin: cDNA and Derived Protein Sequences [J].
Hu, C. -C. ;
Simmer, J. P. ;
Bartlett, J. D. ;
Qian, Q. ;
Zhang, C. ;
Ryu, O. H. ;
Xue, J. ;
Fukae, M. ;
Uchida, T. ;
MacDougall, M. .
CONNECTIVE TISSUE RESEARCH, 1998, 39 (1-3) :47-61
[18]   A comparison of enamelin and amelogenin expression in developing mouse molars [J].
Hu, JCC ;
Sun, XL ;
Zhang, CH ;
Simmer, JP .
EUROPEAN JOURNAL OF ORAL SCIENCES, 2001, 109 (02) :125-132
[19]   Autosomal-dominant hypoplastic form of amelogenesis imperfecta caused by an enamelin gene mutation at the exon-intron boundary [J].
Kida, M ;
Ariga, T ;
Shirakawa, T ;
Oguchi, H ;
Sakiyama, Y .
JOURNAL OF DENTAL RESEARCH, 2002, 81 (11) :738-742
[20]  
Kikkawa Y, 2000, J CELL SCI, V113, P869