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腭发育的分子和细胞机制

Molecular and Cellular Mechanisms of Palate Development.

作者信息

Li C, Lan Y, Jiang R

机构信息

1 Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.

2 Division of Plastic Surgery, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.

出版信息

J Dent Res. 2017 Oct;96(11):1184-1191. doi: 10.1177/0022034517703580. Epub 2017 Jul 26.

DOI:10.1177/0022034517703580
PMID:28745929
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5613875/
Abstract

Development of the mammalian secondary palate involves highly dynamic morphogenetic processes, including outgrowth of palatal shelves from the oral side of the embryonic maxillary prominences, elevation of the initially vertically oriented palatal shelves to the horizontal position above the embryonic tongue, and subsequently adhesion and fusion of the paired palatal shelves at the midline to separate the oral cavity from the nasal cavity. Perturbation of any of these processes could cause cleft palate, a common birth defect that significantly affects patients' quality of life even after surgical treatment. In addition to identifying a large number of genes required for palate development, recent studies have begun to unravel the extensive cross-regulation of multiple signaling pathways, including Sonic hedgehog, bone morphogenetic protein, fibroblast growth factor, transforming growth factor β, and Wnt signaling, and multiple transcription factors during palatal shelf growth and patterning. Multiple studies also provide new insights into the gene regulatory networks and/or dynamic cellular processes underlying palatal shelf elevation, adhesion, and fusion. Here we summarize major recent advances and integrate the genes and molecular pathways with the cellular and morphogenetic processes of palatal shelf growth, patterning, elevation, adhesion, and fusion.

摘要

哺乳动物次生腭的发育涉及高度动态的形态发生过程,包括腭突从胚胎上颌突的口腔侧长出、最初垂直定向的腭突上升到胚胎舌上方的水平位置,以及随后成对的腭突在中线处黏附并融合,从而将口腔与鼻腔分隔开。这些过程中的任何一个受到干扰都可能导致腭裂,这是一种常见的出生缺陷,即使在手术治疗后也会严重影响患者的生活质量。除了鉴定出大量腭发育所需的基因外,最近的研究还开始揭示多种信号通路(包括 Sonic hedgehog、骨形态发生蛋白、成纤维细胞生长因子、转化生长因子β和Wnt信号通路)以及多种转录因子在腭突生长和模式形成过程中的广泛交叉调节。多项研究还为腭突上升、黏附及融合背后的基因调控网络和/或动态细胞过程提供了新见解。在此,我们总结近期的主要进展,并将基因和分子通路与腭突生长、模式形成、上升、黏附及融合的细胞和形态发生过程整合起来。

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本文引用的文献

1
Coordinately Co-opted Multiple Transposable Elements Constitute an Enhancer for wnt5a Expression in the Mammalian Secondary Palate.协同被招募的多个转座元件构成了哺乳动物次生腭中wnt5a表达的一个增强子。
PLoS Genet. 2016 Oct 14;12(10):e1006380. doi: 10.1371/journal.pgen.1006380. eCollection 2016 Oct.
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Mesenchymal Remodeling during Palatal Shelf Elevation Revealed by Extracellular Matrix and F-Actin Expression Patterns.通过细胞外基质和F-肌动蛋白表达模式揭示的腭突抬高过程中的间充质重塑
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Wnt Signaling in Cell Motility and Invasion: Drawing Parallels between Development and Cancer.Wnt 信号在细胞迁移和侵袭中的作用:发育与癌症之间的平行关系。
Cancers (Basel). 2016 Aug 29;8(9):80. doi: 10.3390/cancers8090080.
4
Golgb1 regulates protein glycosylation and is crucial for mammalian palate development.高尔基体蛋白1(Golgb1)调节蛋白质糖基化,对哺乳动物腭部发育至关重要。
Development. 2016 Jul 1;143(13):2344-55. doi: 10.1242/dev.134577. Epub 2016 May 25.
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Foxf2 is required for secondary palate development and Tgfβ signaling in palatal shelf mesenchyme.Foxf2是次生腭发育和腭突间充质中Tgfβ信号传导所必需的。
Dev Biol. 2016 Jul 1;415(1):14-23. doi: 10.1016/j.ydbio.2016.05.013. Epub 2016 May 13.
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A Shh-Foxf-Fgf18-Shh Molecular Circuit Regulating Palate Development.一个调控腭发育的Shh-Foxf-Fgf18-Shh分子回路
PLoS Genet. 2016 Jan 8;12(1):e1005769. doi: 10.1371/journal.pgen.1005769. eCollection 2016 Jan.
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Mapping cellular processes in the mesenchyme during palatal development in the absence of Tbx1 reveals complex proliferation changes and perturbed cell packing and polarity.在缺乏Tbx1的情况下,绘制腭发育过程中间充质中的细胞过程,揭示了复杂的增殖变化以及细胞堆积和极性的紊乱。
J Anat. 2016 Mar;228(3):464-73. doi: 10.1111/joa.12425. Epub 2015 Dec 22.
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Cellular and Molecular Mechanisms of Palatogenesis.腭发育的细胞和分子机制
Curr Top Dev Biol. 2015;115:59-84. doi: 10.1016/bs.ctdb.2015.07.002. Epub 2015 Oct 1.
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Toward an orofacial gene regulatory network.构建口腔面部基因调控网络。
Dev Dyn. 2016 Mar;245(3):220-32. doi: 10.1002/dvdy.24341. Epub 2015 Sep 17.
10
IRF6 is the mediator of TGFβ3 during regulation of the epithelial mesenchymal transition and palatal fusion.IRF6是上皮-间质转化和腭融合调节过程中TGFβ3的介质。
Sci Rep. 2015 Aug 4;5:12791. doi: 10.1038/srep12791.