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-1α. 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-1α is expressed and transcriptionally active in limb bud mesenchyme and in mesenchymal condensations. To investigate the role of Hif-1α in mesenchymal condensations and in early chondrogenesis, we conditionally inactivated Hif-1α in limb bud mesenchyme using a Prx1 promoter-driven Cre transgenic mouse. Conditional knockout of Hif-1α 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-1α in early chondrogenesis and joint formation.
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7 May 2007
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April 30 2007
Hif-1α regulates differentiation of limb bud mesenchyme and joint development
Sylvain Provot,
Sylvain Provot
1Endocrine Unit, Department of Medicine, Massachusetts General Hospital-Harvard Medical School, Boston, MA 02114
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Dawn Zinyk,
Dawn Zinyk
2Division of Cancer and Radiation Biology, Department of Radiation Oncology, Stanford University School of Medicine, Stanford, CA 94305
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Yasemin Gunes,
Yasemin Gunes
1Endocrine Unit, Department of Medicine, Massachusetts General Hospital-Harvard Medical School, Boston, MA 02114
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Richa Kathri,
Richa Kathri
1Endocrine Unit, Department of Medicine, Massachusetts General Hospital-Harvard Medical School, Boston, MA 02114
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Quynh Le,
Quynh Le
2Division of Cancer and Radiation Biology, Department of Radiation Oncology, Stanford University School of Medicine, Stanford, CA 94305
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Henry M. Kronenberg,
Henry M. Kronenberg
1Endocrine Unit, Department of Medicine, Massachusetts General Hospital-Harvard Medical School, Boston, MA 02114
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Randall S. Johnson,
Randall S. Johnson
3Molecular Biology Section, University of California, San Diego, La Jolla, CA 92093
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Michael T. Longaker,
Michael T. Longaker
2Division of Cancer and Radiation Biology, Department of Radiation Oncology, Stanford University School of Medicine, Stanford, CA 94305
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Amato J. Giaccia,
Amato J. Giaccia
2Division of Cancer and Radiation Biology, Department of Radiation Oncology, Stanford University School of Medicine, Stanford, CA 94305
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Ernestina Schipani
Ernestina Schipani
1Endocrine Unit, Department of Medicine, Massachusetts General Hospital-Harvard Medical School, Boston, MA 02114
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Sylvain Provot
1Endocrine Unit, Department of Medicine, Massachusetts General Hospital-Harvard Medical School, Boston, MA 02114
Dawn Zinyk
2Division of Cancer and Radiation Biology, Department of Radiation Oncology, Stanford University School of Medicine, Stanford, CA 94305
Yasemin Gunes
1Endocrine Unit, Department of Medicine, Massachusetts General Hospital-Harvard Medical School, Boston, MA 02114
Richa Kathri
1Endocrine Unit, Department of Medicine, Massachusetts General Hospital-Harvard Medical School, Boston, MA 02114
Quynh Le
2Division of Cancer and Radiation Biology, Department of Radiation Oncology, Stanford University School of Medicine, Stanford, CA 94305
Henry M. Kronenberg
1Endocrine Unit, Department of Medicine, Massachusetts General Hospital-Harvard Medical School, Boston, MA 02114
Randall S. Johnson
3Molecular Biology Section, University of California, San Diego, La Jolla, CA 92093
Michael T. Longaker
2Division of Cancer and Radiation Biology, Department of Radiation Oncology, Stanford University School of Medicine, Stanford, CA 94305
Amato J. Giaccia
2Division of Cancer and Radiation Biology, Department of Radiation Oncology, Stanford University School of Medicine, Stanford, CA 94305
Ernestina Schipani
1Endocrine Unit, Department of Medicine, Massachusetts General Hospital-Harvard Medical School, Boston, MA 02114
Correspondence to Amato J. Giaccia: [email protected]
S. Provot and D. Zinyk contributed equally to this paper.
Abbreviations used in this paper: CKO, conditional knockout; E, embryonic day; Hif-1α, hypoxia-inducible factor 1α; HRE, hypoxia response element; H&E, hematoxylin and eosin; Ihh, Indian hedgehog; P, postnatal day; p4haI, prolyl-4-hydroxylase α (I); PNA, Peanut agglutinin; VEGFR2, VEGF-receptor2.
Received:
December 04 2006
Accepted:
March 26 2007
Online ISSN: 1540-8140
Print ISSN: 0021-9525
The Rockefeller University Press
2007
J Cell Biol (2007) 177 (3): 451–464.
Article history
Received:
December 04 2006
Accepted:
March 26 2007
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Citation
Sylvain Provot, Dawn Zinyk, Yasemin Gunes, Richa Kathri, Quynh Le, Henry M. Kronenberg, Randall S. Johnson, Michael T. Longaker, Amato J. Giaccia, Ernestina Schipani; Hif-1α regulates differentiation of limb bud mesenchyme and joint development . J Cell Biol 7 May 2007; 177 (3): 451–464. doi: https://doi.org/10.1083/jcb.200612023
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