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叉头因子HFH-4基因敲除小鼠的纤毛发生与左右轴缺陷

Ciliogenesis and left-right axis defects in forkhead factor HFH-4-null mice.

作者信息

Brody S L, Yan X H, Wuerffel M K, Song S K, Shapiro S D

机构信息

Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.

出版信息

Am J Respir Cell Mol Biol. 2000 Jul;23(1):45-51. doi: 10.1165/ajrcmb.23.1.4070.

DOI:10.1165/ajrcmb.23.1.4070
PMID:10873152
Abstract

Cilia have been classified as sensory or motile types on the basis of functional and structural characteristics; however, factors important for regulation of assembly of different cilia types are not well understood. Hepatocyte nuclear factor-3/forkhead homologue 4 (HFH-4) is a winged helix/forkhead transcription factor expressed in ciliated cells of the respiratory tract, oviduct, and ependyma in late development through adulthood. Targeted deletion of the Hfh4 gene resulted in defective ciliogenesis in airway epithelial cells and randomized left-right asymmetry so that half the mice had situs inversus. In HFH-4-null mice, classic motile type cilia with a 9 + 2 microtubule ultrastructure were absent in epithelial cells, including those in the airways. In other organs, sensory cilia with a 9 + 0 microtubule pattern, such as those on olfactory neuroepithelial cells, were present. Ultrastructural analysis of mutant cells with absent 9 + 2 cilia demonstrated that defective ciliogenesis was due to abnormal centriole migration and/or apical membrane docking, suggesting that HFH-4 functions to direct basal body positioning or anchoring. Evaluation of wild-type embryos at gestational days 7.0 to 7.5 revealed Hfh4 expression in embryonic node cells that have monocilium, consistent with a function for this factor at the node in early determination of left- right axis. Analysis of the node of HFH-4 mutant embryos revealed that, in contrast to absent airway cilia, node cilia were present. These observations indicate that there are independent regulatory pathways for node ciliogenesis compared with 9 + 2 type ciliogenesis in airways, and support a central role for HFH-4 in ciliogenesis and left-right axis formation.

摘要

根据功能和结构特征,纤毛可分为感觉型或运动型;然而,对于不同类型纤毛组装调控的重要因素,我们还了解得不够透彻。肝细胞核因子-3/叉头同源物4(HFH-4)是一种翼状螺旋/叉头转录因子,在发育后期直至成年期,呼吸道、输卵管和室管膜的纤毛细胞中均有表达。靶向缺失Hfh4基因会导致气道上皮细胞纤毛发生缺陷,左右不对称随机化,使得一半的小鼠出现内脏反位。在HFH-4基因敲除小鼠中,上皮细胞(包括气道上皮细胞)中不存在具有9 + 2微管超微结构的典型运动型纤毛。在其他器官中,存在具有9 + 0微管模式的感觉纤毛,如嗅觉神经上皮细胞上的纤毛。对缺乏9 + 2纤毛的突变细胞进行超微结构分析表明,纤毛发生缺陷是由于中心粒迁移异常和/或顶端膜对接异常,这表明HFH-4的功能是指导基体定位或锚定。对妊娠第7.0至7.5天的野生型胚胎进行评估,发现在具有单纤毛的胚胎节点细胞中有Hfh4表达,这与该因子在早期确定左右轴的节点处发挥的功能一致。对HFH-4突变胚胎的节点进行分析发现,与气道中不存在纤毛不同,节点纤毛是存在的。这些观察结果表明,与气道中9 + 2型纤毛发生相比,节点纤毛发生存在独立的调控途径,并支持HFH-4在纤毛发生和左右轴形成中发挥核心作用。

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