Department of Pediatric Surgery, Erasmus MC-Sophia Children's Hospital, Rotterdam, The Netherlands.
PLoS One. 2013;8(2):e57695. doi: 10.1371/journal.pone.0057695. Epub 2013 Feb 25.
Lung development occurs under relative hypoxia and the most important oxygen-sensitive response pathway is driven by Hypoxia Inducible Factors (HIF). HIFs are heterodimeric transcription factors of an oxygen-sensitive subunit, HIFα, and a constitutively expressed subunit, HIF1β. HIF1α and HIF2α, encoded by two separate genes, contribute to the activation of hypoxia inducible genes. A third HIFα gene, HIF3α, is subject to alternative promoter usage and splicing, leading to three major isoforms, HIF3α, NEPAS and IPAS. HIF3α gene products add to the complexity of the hypoxia response as they function as dominant negative inhibitors (IPAS) or weak transcriptional activators (HIF3α/NEPAS). Previously, we and others have shown the importance of the Hif1α and Hif2α factors in lung development, and here we investigated the role of Hif3α during pulmonary development. Therefore, HIF3α was conditionally expressed in airway epithelial cells during gestation and although HIF3α transgenic mice were born alive and appeared normal, their lungs showed clear abnormalities, including a post-pseudoglandular branching defect and a decreased number of alveoli. The HIF3α expressing lungs displayed reduced numbers of Clara cells, alveolar epithelial type I and type II cells. As a result of HIF3α expression, the level of Hif2α was reduced, but that of Hif1α was not affected. Two regulatory genes, Rarβ, involved in alveologenesis, and Foxp2, a transcriptional repressor of the Clara cell specific Ccsp gene, were significantly upregulated in the HIF3α expressing lungs. In addition, aberrant basal cells were observed distally as determined by the expression of Sox2 and p63. We show that Hif3α binds a conserved HRE site in the Sox2 promoter and weakly transactivated a reporter construct containing the Sox2 promoter region. Moreover, Hif3α affected the expression of genes not typically involved in the hypoxia response, providing evidence for a novel function of Hif3α beyond the hypoxia response.
肺的发育是在相对缺氧的条件下进行的,最重要的氧敏感反应途径是由缺氧诱导因子(HIF)驱动的。HIF 是由一个氧敏感亚基 HIFα和一个组成型表达的亚基 HIF1β组成的异二聚体转录因子。HIF1α 和 HIF2α 由两个独立的基因编码,有助于激活缺氧诱导基因。第三个 HIFα 基因 HIF3α 受替代启动子使用和剪接的影响,导致三种主要的同工型 HIF3α、NEPAS 和 IPAS。HIF3α 基因产物增加了缺氧反应的复杂性,因为它们作为显性负抑制剂(IPAS)或弱转录激活剂(HIF3α/NEPAS)发挥作用。以前,我们和其他人已经表明 Hif1α 和 Hif2α 因子在肺发育中的重要性,在这里我们研究了 Hif3α 在肺发育过程中的作用。因此,HIF3α 在妊娠期气道上皮细胞中条件性表达,尽管 HIF3α 转基因小鼠出生时存活并表现正常,但它们的肺显示出明显的异常,包括假腺期后分支缺陷和肺泡数量减少。表达 HIF3α 的肺显示出 Clara 细胞、肺泡上皮 I 型和 II 型细胞数量减少。由于 HIF3α 的表达,Hif2α 的水平降低,但 Hif1α 的水平不受影响。两个调节基因,Rarβ,参与肺泡发生,以及 Foxp2,Clara 细胞特异性 Ccsp 基因的转录抑制因子,在表达 HIF3α 的肺中显著上调。此外,通过 Sox2 和 p63 的表达,在远端观察到异常的基底细胞。我们表明,Hif3α 结合 Sox2 启动子中的保守 HRE 位点,并弱转录激活包含 Sox2 启动子区域的报告基因构建体。此外,Hif3α 影响通常不参与缺氧反应的基因的表达,为 Hif3α 超越缺氧反应的新功能提供了证据。