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Zfp521 antagonizes Runx2, delays osteoblast differentiation in vitro, and promotes bone formation in vivo
被引:62
|作者:
Wu, Meilin
[2
,4
]
Hesse, Eric
[2
,3
]
Morvan, Frederic
[2
,5
]
Zhang, Jian-Ping
[2
]
Correa, Diego
[2
,3
]
Rowe, Glenn C.
[2
,3
]
Kiviranta, Riku
[2
,3
]
Neff, Lynn
[2
]
Philbrick, William M.
[2
]
Horne, William C.
[2
,3
]
Baron, Roland
[1
,2
,3
]
机构:
[1] Harvard Univ, Sch Dent Med, Dept Oral Med Infect & Immun, Boston, MA 02115 USA
[2] Yale Univ, Sch Med, New Haven, CT 06510 USA
[3] Harvard Univ, Sch Med, Boston, MA 02115 USA
[4] Mol Cardiol Res Ctr, Div Cardiovasc, Philadelphia, PA 19104 USA
[5] Musculoskeletal Dis Area, Novartis Inst Biomed Res, CH-4057 Basel, Switzerland
来源:
基金:
芬兰科学院;
美国国家卫生研究院;
关键词:
Zfp521;
Runx2;
Osteoblast;
Bone formation;
Differentiation;
ZINC-FINGER PROTEIN;
OSTEOCALCIN GENE;
BETA-CATENIN;
TRANSCRIPTION FACTOR;
KS483;
CELLS;
EXPRESSION;
OVEREXPRESSION;
CBFA1;
TARGET;
ADIPOGENESIS;
D O I:
10.1016/j.bone.2008.11.011
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Zfp521, a 30 C2H2 Kruppel-like zinc finger protein, is expressed at high levels at the periphery of early mesenchymal condensations prefiguring skeletal elements and in all developing bones in the perichondrium and periosteum, in osteoblast precursors and osteocytes, and in chondroblast precursors and growth plate prehypertrophic chondrocytes. Zfp521 expression in cultured mesenchymal cells is decreased by BMP-2 and increased by PTHrP, which promote and antagonize osteoblast differentiation, respectively. In vitro, Zfp521 overexpression reduces the expression of several downstream osteoblast marker genes and antagonizes osteoblast differentiation. Zfp521 binds Runx2 and represses its transcriptional activity, and Runx2 dose-dependently rescues Zfp521's inhibition of osteoblast differentiation. In contrast, osteocalcin promoter-targeted overexpression of Zfp521 in osteoblasts in vivo results in increased bone formation and bone mass, We propose that Zfp521 regulates the rate of osteoblast differentiation and bone formation during development and in the mature skeleton, in part by antagonizing Runx2. (C) 2008 Elsevier Inc. All rights reserved.
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页码:528 / 536
页数:9
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