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
[1]   The transcrintion factor Sox9 has essential roles in successive steps of the chondrocyte differentiation pathway and is required for expression of Sox5 and Sox6 [J].
Akiyama, H ;
Chaboissier, MC ;
Martin, JF ;
Schedl, A ;
de Crombrugghe, B .
GENES & DEVELOPMENT, 2002, 16 (21) :2813-2828
[2]   Haploinsufficiency of Sox9 results in defective cartilage primordia and premature skeletal mineralization [J].
Bi, WM ;
Huang, WD ;
Whitworth, DJ ;
Deng, JM ;
Zhang, ZP ;
Behringer, RR ;
de Crombrugghe, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (12) :6698-6703
[3]   Sox9 is required for cartilage formation [J].
Bi, WM ;
Deng, JM ;
Zhang, ZP ;
Behringer, RR ;
de Crombrugghe, B .
NATURE GENETICS, 1999, 22 (01) :85-89
[4]   Genetic analysis of pathways regulated by the von Hippel-Lindau tumor suppressor in Caenorhabditis elegans [J].
Bishop, T ;
Lau, KW ;
Epstein, ACR ;
Kim, SK ;
Min, J ;
O'Rourke, D ;
Pugh, CW ;
Gleadle, JM ;
Taylor, MS ;
Hodgkin, J ;
Ratcliffe, PJ .
PLOS BIOLOGY, 2004, 2 (10) :1549-1560
[5]   Noggin, cartilage morphogenesis, and joint formation in the mammalian skeleton [J].
Brunet, LJ ;
McMahon, JA ;
McMahon, AP ;
Harland, RM .
SCIENCE, 1998, 280 (5368) :1455-1457
[6]   Oxygen sensing and molecular adaptation to hypoxia [J].
Bunn, HF ;
Poyton, RO .
PHYSIOLOGICAL REVIEWS, 1996, 76 (03) :839-885
[7]   Role of prolyl hydroxylation in oncogenically stabilized hypoxia-inducible factor-1α [J].
Chan, DA ;
Sutphin, PD ;
Denko, NC ;
Giaccia, AJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (42) :40112-40117
[8]  
Chen EY, 1999, TERATOLOGY, V60, P215
[9]   Regulatory mechanisms in the pathways of cartilage and bone formation [J].
de Crombrugghe, B ;
Lefebvre, W .
CURRENT OPINION IN CELL BIOLOGY, 2001, 13 (06) :721-727
[10]   TOWARD A MOLECULAR UNDERSTANDING OF SKELETAL DEVELOPMENT [J].
ERLEBACHER, A ;
FILVAROFF, EH ;
GITELMAN, SE ;
DERYNCK, R .
CELL, 1995, 80 (03) :371-378