Hif-1α regulates differentiation of limb bud mesenchyme and joint development

被引:156
作者
Provot, Sylvain
Zinyk, Dawn
Gunes, Yasemin
Kathri, Richa
Le, Quynh
Kronenberg, Henry M.
Johnson, Randall S.
Longaker, Michael T.
Giaccia, Amato J. [1 ]
Schipani, Ernestina
机构
[1] Stanford Univ, Sch Med, Div Canc & Radiat Biol, Dept Radiat Oncol, Stanford, CA 94305 USA
[2] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Dept Med,Endocrine Unit, Boston, MA 02114 USA
[3] Univ Calif San Diego, Mol Biol Sect, La Jolla, CA 92093 USA
关键词
D O I
10.1083/jcb.200612023
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Recent evidence suggests that low oxygen tension (hypoxia) may control fetal development and differentiation. A crucial mediator of the adaptive response of cells to hypoxia is the transcription factor Hif-1 alpha In this study, we provide evidence that mesenchymal condensations that give origin to endochondral bones are hypoxic during fetal development, and we demonstrate that Hif-1 alpha is expressed and transcriptionally active in limb bud mesenchyme and in mesenchymal condensations. To investigate the role of Hif-1 alpha in mesenchymal condensations and in early chondrogenesis, we conditionally inactivated Hif-1 alpha in limb bud mesenchyme using a Prx1 promoter-driven Cre transgenic mouse. Conditional knockout of Hif-1 alpha in limb bud mesenchyme does not impair mesenchyme condensation, but alters the formation of the cartilaginous primordia. Late hypertrophic differentiation is also affected as a result of the delay in early chondrogenesis. In addition, mutant mice show a striking impairment of joint development. Our study demonstrates a crucial, and previously unrecognized, role of Hif-1 alpha in early chondrogenesis and joint formation.
引用
收藏
页码:451 / 464
页数:14
相关论文
共 64 条
[11]   The biology of VEGF and its receptors [J].
Ferrara, N ;
Gerber, HP ;
LeCouter, J .
NATURE MEDICINE, 2003, 9 (06) :669-676
[12]   VEGF couples hypertrophic cartilage remodeling, ossification and angiogenesis during endochondral bone formation [J].
Gerber, HP ;
Vu, TH ;
Ryan, AM ;
Kowalski, J ;
Werb, Z ;
Ferrara, N .
NATURE MEDICINE, 1999, 5 (06) :623-628
[13]   HIF-1 as a target for drug development [J].
Giaccia, A ;
Siim, BG ;
Johnson, RS .
NATURE REVIEWS DRUG DISCOVERY, 2003, 2 (10) :803-811
[14]   The biology of hypoxia: the role of oxygen sensing in development, normal function, and disease [J].
Giaccia, AJ ;
Simon, MC ;
Johnson, R .
GENES & DEVELOPMENT, 2004, 18 (18) :2183-2194
[15]   Up-regulation of gene expression by hypoxia is mediated predominantly by hypoxia-inducible factor 1 (HIF-1) [J].
Greijer, AE ;
van der Groep, P ;
Kemming, D ;
Shvarts, A ;
Semenza, GL ;
Meijer, GA ;
van de Wiel, MA ;
Belien, JAM ;
van Diest, PJ ;
van der Wall, E .
JOURNAL OF PATHOLOGY, 2005, 206 (03) :291-304
[16]   Wnt/β-catenin signaling is sufficient and necessary for synovial joint formation [J].
Guo, XZ ;
Day, TF ;
Jiang, XY ;
Garrett-Beal, L ;
Topol, L ;
Yang, YZ .
GENES & DEVELOPMENT, 2004, 18 (19) :2404-2417
[17]   Inhibition of terminal chondrocyte differentiation by bone morphogenetic protein 7 (OP-1) in vitro depends on the periarticular region but is independent of parathyroid hormone-related peptide [J].
Haaijman, A ;
Karperien, M ;
Lanske, B ;
Hendriks, J ;
Löwik, CWGM ;
Bronckers, ALJJ ;
Burger, EH .
BONE, 1999, 25 (04) :397-404
[18]   Wnt-14 plays a pivotal role in inducing synovial joint formation in the developing appendicular skeleton [J].
Hartmann, C ;
Tabin, CJ .
CELL, 2001, 104 (03) :341-351
[19]   Oxygen tension regulates chondrocyte differentiation and function during endochondral ossification [J].
Hirao, Makoto ;
Tamai, Noriyuki ;
Tsumaki, Noriyuki ;
Yoshikawa, Hideki ;
Myoui, Akira .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (41) :31079-31092
[20]   HIFα targeted for VHL-mediated destruction by proline hydroxylation:: Implications for O2 sensing [J].
Ivan, M ;
Kondo, K ;
Yang, HF ;
Kim, W ;
Valiando, J ;
Ohh, M ;
Salic, A ;
Asara, JM ;
Lane, WS ;
Kaelin, WG .
SCIENCE, 2001, 292 (5516) :464-468