Matrix metalloproteinases have a role in palatogenesis

被引:46
作者
Brown, NL [1 ]
Yarram, SJ [1 ]
Mansell, JP [1 ]
Sandy, JR [1 ]
机构
[1] Univ Bristol, Sch Dent, Div Child Dent Hlth, Bristol BS1 2LY, Avon, England
关键词
palate; MMP-2; MMP-3;
D O I
10.1177/154405910208101206
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Mammalian palatogenesis depends on palatal shelf elevation, medial edge epithelium (MEE) breakdown, and mesenchyme flow. These all require matrix remodeling, which is controlled in part by the family of matrix metalloproteinases (MMPs). We used an organ culture system to examine the effect of a general MMP inhibitor (BB3103) on mouse palatogenesis. Palates cultured in 20 muM BB3103 contained no active MMP-2, and only one palate fused from a sample size of 15. In this single palate, MMP-3 was present at higher levels than in palates that failed to fuse. MMP-3 is known to be involved in epithelial mesenchymal transformation (EMT), and its persistence may explain why this palate fused. This implies a role for MMPs in normal palatogenesis, and disruption of their activity may result in cleft palate.
引用
收藏
页码:826 / 830
页数:5
相关论文
共 16 条
[1]   DEVELOPMENT OF A SUSPENSION ORGAN-CULTURE OF THE FETAL-RAT PALATE [J].
ALOBAIDI, N ;
KASTNER, U ;
MERKER, HJ ;
KLUG, S .
ARCHIVES OF TOXICOLOGY, 1995, 69 (07) :472-479
[2]   TGF-β3-induced palatogenesis requires matrix metalloproteinases [J].
Blavier, L ;
Lazaryev, A ;
Groffen, J ;
Heisterkamp, N ;
DeClerck, YA ;
Kaartinen, V .
MOLECULAR BIOLOGY OF THE CELL, 2001, 12 (05) :1457-1466
[3]  
BRINKLEY LL, 1980, CURRENT RES TRENDS P, P203
[4]  
FERGUSON MWJ, 1988, DEVELOPMENT, V103, P41
[5]   Unaltered secretion of beta-amyloid precursor protein in gelatinase a (matrix metalloproteinase 2)-deficient mice [J].
Itoh, T ;
Ikeda, T ;
Gomi, H ;
Nakao, S ;
Suzuki, T ;
Itohara, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (36) :22389-22392
[6]  
Knauper V, 1998, BIOL EXTRAC, P199
[7]   Matrix metalloproteinase stromelysin-1 triggers a cascade of molecular alterations that leads to stable epithelial-to-mesenchymal conversion and a premalignant phenotype in mammary epithelial cells [J].
Lochter, A ;
Galosy, S ;
Muschler, J ;
Freedman, N ;
Werb, Z ;
Bissell, MJ .
JOURNAL OF CELL BIOLOGY, 1997, 139 (07) :1861-1872
[8]   Temporal changes in collagen composition and metabolism during rodent palatogenesis [J].
Mansell, JP ;
Kerrigan, J ;
McGill, J ;
Bailey, J ;
TeKoppele, J ;
Sandy, JR .
MECHANISMS OF AGEING AND DEVELOPMENT, 2000, 119 (1-2) :49-62
[9]   Medial edge epithelial cell fate during palatal fusion [J].
Martínez-Alvarez, C ;
Tudela, C ;
Pérez-Miguelsanz, J ;
O'Kane, S ;
Puerta, J ;
Ferguson, MWJ .
DEVELOPMENTAL BIOLOGY, 2000, 220 (02) :343-357
[10]   Epidermal growth factor receptor function is necessary for normal craniofacial development and palate closure [J].
Miettinen, PJ ;
Chin, JR ;
Shum, L ;
Slavkin, HC ;
Shuler, CF ;
Derynck, R ;
Werb, Z .
NATURE GENETICS, 1999, 22 (01) :69-73