Regulatory mechanisms in the pathways of cartilage and bone formation

被引:378
作者
de Crombrugghe, B
Lefebvre, W
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Mol Genet, Houston, TX 77030 USA
[2] Cleveland Clin Fdn, Lerner Res Inst, Dept Biomed Engn, Cleveland, OH 44195 USA
关键词
D O I
10.1016/S0955-0674(00)00276-3
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Three transcription factors of the Sox family have essential roles in different steps of the chondrocyte differentiation pathway. Because the transcription factor Cbfa1, which is needed for osteoblast differentiation, also stimulates hypertrophic chondrocyte maturation, it links the chondrocyte and osteoblast differentiation pathways in endochondral bone formation. Signaling molecules, including Indian Hedgehog, PTHrP and FGFs, also establish essential links either between these pathways, between steps in these pathways or between signaling molecules and transcription factors, so that a more comprehensive view of endochondral bone formation is emerging.
引用
收藏
页码:721 / 727
页数:7
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共 71 条
  • [41] Naski MC, 1998, DEVELOPMENT, V125, P4977
  • [42] SOX9 binds DNA, activates transcription, and coexpresses with type II collagen during chondrogenesis in the mouse
    Ng, LJ
    Wheatley, S
    Muscat, GEO
    ConwayCampbell, J
    Bowles, J
    Wright, E
    Bell, DM
    Tam, PPL
    Cheah, KSE
    Koopman, P
    [J]. DEVELOPMENTAL BIOLOGY, 1997, 183 (01) : 108 - 121
  • [43] Bone development
    Olsen, BR
    Reginato, AM
    Wang, WF
    [J]. ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 2000, 16 : 191 - 220
  • [44] Muscle minus MyoD
    Olson, EN
    Klein, WH
    [J]. DEVELOPMENTAL BIOLOGY, 1998, 202 (02) : 153 - 156
  • [45] Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development
    Otto, F
    Thornell, AP
    Crompton, T
    Denzel, A
    Gilmour, KC
    Rosewell, IR
    Stamp, GWH
    Beddington, RSP
    Mundlos, S
    Olsen, BR
    Selby, PB
    Owen, MJ
    [J]. CELL, 1997, 89 (05) : 765 - 771
  • [46] P53-INDEPENDENT EXPRESSION OF P21(CIP)1 IN MUSCLE AND OTHER TERMINALLY DIFFERENTIATING CELLS
    PARKER, SB
    EICHELE, G
    ZHANG, PM
    RAWLS, A
    SANDS, AT
    BRADLEY, A
    OLSON, EN
    HARPER, JW
    ELLEDGE, SJ
    [J]. SCIENCE, 1995, 267 (5200) : 1024 - 1027
  • [47] Autosomal dominant craniometaphyseal dysplasia is caused by mutations in the transmembrane protein ANK
    Reichenberger, E
    Tiziani, V
    Watanabe, S
    Park, L
    Ueki, Y
    Santanna, C
    Baur, ST
    Shiang, R
    Grange, DK
    Beighton, P
    Gardner, J
    Hamersma, H
    Sellars, S
    Ramesar, R
    Lidral, AC
    Sommer, A
    do Amaral, CMR
    Gorlin, RJ
    Mulliken, JB
    Olsen, BR
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 68 (06) : 1321 - 1326
  • [48] Molecular regulation of adipogenesis
    Rosen, ED
    Spiegelman, BM
    [J]. ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 2000, 16 : 145 - 171
  • [49] STOP CODON FGFR3 MUTATIONS IN THANATOPHORIC DWARFISM TYPE-1
    ROUSSEAU, F
    SAUGIER, P
    LEMERRER, M
    MUNNICH, A
    DELEZOIDE, AL
    MAROTEAUX, P
    BONAVENTURE, J
    NARCY, F
    SANAK, M
    [J]. NATURE GENETICS, 1995, 10 (01) : 11 - 12
  • [50] MUTATIONS IN THE GENE ENCODING FIBROBLAST GROWTH-FACTOR RECEPTOR-3 IN ACHONDROPLASIA
    ROUSSEAU, F
    BONAVENTURE, J
    LEGEAIMALLET, L
    PELET, A
    ROZET, JM
    MAROTEAUX, P
    LEMERRER, M
    MUNNICH, A
    [J]. NATURE, 1994, 371 (6494) : 252 - 254