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
[1]  
ADAMS JC, 1993, DEVELOPMENT, V117, P1183
[2]   Laminin α5 chain is required for intestinal smooth muscle development [J].
Bolcato-Bellemin, AL ;
Lefebvre, O ;
Arnold, C ;
Sorokin, L ;
Miner, JH ;
Kedinger, M ;
Simon-Assmann, P .
DEVELOPMENTAL BIOLOGY, 2003, 260 (02) :376-390
[3]   Immunolocalization of epithelial and mesenchymal matrix constituents in association with inner enamel epithelial cells [J].
Bosshardt, DD ;
Nanci, A .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1998, 46 (02) :135-142
[4]   DISTINCT FUNCTIONS FOR INTEGRINS ALPHA-3-BETA-1 IN FOCAL ADHESIONS AND ALPHA-6-BETA-4 BULLOUS PEMPHIGOID ANTIGEN IN A NEW STABLE ANCHORING CONTACT (SAC) OF KERATINOCYTES - RELATION TO HEMIDESMOSOMES [J].
CARTER, WG ;
KAUR, P ;
GIL, SG ;
GAHR, PJ ;
WAYNER, EA .
JOURNAL OF CELL BIOLOGY, 1990, 111 (06) :3141-3154
[5]  
Cerny R, 1996, J BONE MINER RES, V11, P883
[6]   DEVELOPMENT OF THE MOLAR TEETH IN THE ALBINO MOUSE [J].
COHN, SA .
AMERICAN JOURNAL OF ANATOMY, 1957, 101 (02) :295-319
[7]   Enamelin maps to human chromosome 4q21 within the autosomal dominant amelogenesis imperfecta locus [J].
Dong, J ;
Gu, TT ;
Simmons, D ;
MacDougall, M .
EUROPEAN JOURNAL OF ORAL SCIENCES, 2000, 108 (05) :353-358
[8]   Tissue-specific expression of the human laminin alpha 5-chain, and mapping of the gene to human chromosome 20q13.2-13.3 and to distal mouse chromosome 2 near the locus for the ragged (Ra) mutation [J].
Durkin, ME ;
Loechel, F ;
Mattei, MG ;
Gilpin, BJ ;
Albrechtsen, R ;
Wewer, UM .
FEBS LETTERS, 1997, 411 (2-3) :296-300
[9]   LAMININ VARIANTS - WHY, WHERE AND WHEN [J].
ENGVALL, E .
KIDNEY INTERNATIONAL, 1993, 43 (01) :2-6
[10]  
Engvall E, 1996, J CELL BIOCHEM, V61, P493