Provot Sylvain, Zinyk Dawn, Gunes Yasemin, Kathri Richa, Le Quynh, Kronenberg Henry M, Johnson Randall S, Longaker Michael T, Giaccia Amato J, Schipani Ernestina
Endocrine Unit, Department of Medicine, Massachusetts General Hospital-Harvard Medical School, Boston, MA 02114, USA.
J Cell Biol. 2007 May 7;177(3):451-64. doi: 10.1083/jcb.200612023. Epub 2007 Apr 30.
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-1alpha. 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-1alpha is expressed and transcriptionally active in limb bud mesenchyme and in mesenchymal condensations. To investigate the role of Hif-1alpha in mesenchymal condensations and in early chondrogenesis, we conditionally inactivated Hif-1alpha in limb bud mesenchyme using a Prx1 promoter-driven Cre transgenic mouse. Conditional knockout of Hif-1alpha 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-1alpha in early chondrogenesis and joint formation.
近期证据表明,低氧张力(缺氧)可能控制胎儿的发育和分化。细胞对缺氧适应性反应的一个关键介质是转录因子Hif-1α。在本研究中,我们提供证据表明,在胎儿发育过程中,产生软骨内骨的间充质凝聚处于缺氧状态,并且我们证明Hif-1α在肢芽间充质和间充质凝聚中表达且具有转录活性。为了研究Hif-1α在间充质凝聚和早期软骨形成中的作用,我们使用Prx1启动子驱动的Cre转基因小鼠,有条件地使肢芽间充质中的Hif-1α失活。肢芽间充质中Hif-1α的条件性敲除不会损害间充质凝聚,但会改变软骨原基的形成。由于早期软骨形成延迟,晚期肥大分化也受到影响。此外,突变小鼠表现出关节发育的显著受损。我们的研究证明了Hif-1α在早期软骨形成和关节形成中起着关键且此前未被认识到的作用。