Sequential roles of Hedgehog and Wnt signaling in osteoblast development
被引:526
作者:
Hu, HL
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机构:Washington Univ, Sch Med, Dept Med, St Louis, MO 63110 USA
Hu, HL
Hilton, MJ
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机构:Washington Univ, Sch Med, Dept Med, St Louis, MO 63110 USA
Hilton, MJ
Tu, XL
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机构:Washington Univ, Sch Med, Dept Med, St Louis, MO 63110 USA
Tu, XL
Yu, K
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机构:Washington Univ, Sch Med, Dept Med, St Louis, MO 63110 USA
Yu, K
Ornitz, DM
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机构:Washington Univ, Sch Med, Dept Med, St Louis, MO 63110 USA
Ornitz, DM
Long, F
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机构:
Washington Univ, Sch Med, Dept Med, St Louis, MO 63110 USAWashington Univ, Sch Med, Dept Med, St Louis, MO 63110 USA
Long, F
[1
]
机构:
[1] Washington Univ, Sch Med, Dept Med, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Mol Biol & Pharmacol, St Louis, MO 63110 USA
来源:
DEVELOPMENT
|
2005年
/
132卷
/
01期
关键词:
Hh;
Wnt;
osteoblast;
mouse;
D O I:
10.1242/dev.01564
中图分类号:
Q [生物科学];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Signals that govern development of the osteoblast lineage are not well understood. Indian hedgehog (Ihh), a member of the hedgehog (Hh) family of proteins, is essential for osteogenesis in the endochondral skeleton during embryogenesis. The canonical pathway of Wnt signaling has been implicated by studies of Lrp5, a co-receptor for Writ proteins, in postnatal bone mass homeostasis. In the present study we demonstrate that beta-catenin, a central player in the canonical Writ pathway, is indispensable for osteoblast differentiation in the mouse embryo. Moreover. we present evidence that Writ signaling functions downstream of Ihh in development of the osteoblast lineage. Finally Wnt7b is identified as a potential endogenous ligand regulating osteogenesis. These data support a model that integrates Hh and Wnt signaling in the regulation of osteoblast development.
机构:
Mem Sloan Kettering Canc Ctr, Sloan Kettering Inst, Cell Biol Program, New York, NY 10021 USAMem Sloan Kettering Canc Ctr, Sloan Kettering Inst, Cell Biol Program, New York, NY 10021 USA
Cong, F
Schweizer, L
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Mem Sloan Kettering Canc Ctr, Sloan Kettering Inst, Cell Biol Program, New York, NY 10021 USAMem Sloan Kettering Canc Ctr, Sloan Kettering Inst, Cell Biol Program, New York, NY 10021 USA
Schweizer, L
Chamorro, M
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机构:
Mem Sloan Kettering Canc Ctr, Sloan Kettering Inst, Cell Biol Program, New York, NY 10021 USAMem Sloan Kettering Canc Ctr, Sloan Kettering Inst, Cell Biol Program, New York, NY 10021 USA
Chamorro, M
Varmus, H
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机构:
Mem Sloan Kettering Canc Ctr, Sloan Kettering Inst, Cell Biol Program, New York, NY 10021 USAMem Sloan Kettering Canc Ctr, Sloan Kettering Inst, Cell Biol Program, New York, NY 10021 USA
机构:
Mem Sloan Kettering Canc Ctr, Sloan Kettering Inst, Cell Biol Program, New York, NY 10021 USAMem Sloan Kettering Canc Ctr, Sloan Kettering Inst, Cell Biol Program, New York, NY 10021 USA
Cong, F
Schweizer, L
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h-index: 0
机构:
Mem Sloan Kettering Canc Ctr, Sloan Kettering Inst, Cell Biol Program, New York, NY 10021 USAMem Sloan Kettering Canc Ctr, Sloan Kettering Inst, Cell Biol Program, New York, NY 10021 USA
Schweizer, L
Chamorro, M
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h-index: 0
机构:
Mem Sloan Kettering Canc Ctr, Sloan Kettering Inst, Cell Biol Program, New York, NY 10021 USAMem Sloan Kettering Canc Ctr, Sloan Kettering Inst, Cell Biol Program, New York, NY 10021 USA
Chamorro, M
Varmus, H
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h-index: 0
机构:
Mem Sloan Kettering Canc Ctr, Sloan Kettering Inst, Cell Biol Program, New York, NY 10021 USAMem Sloan Kettering Canc Ctr, Sloan Kettering Inst, Cell Biol Program, New York, NY 10021 USA