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小鼠作为唇腭裂研究的发育模型。

The mouse as a developmental model for cleft lip and palate research.

作者信息

Gritli-Linde Amel

机构信息

Department of Oral Biochemistry, University of Gothenburg, Göteborg, Sweden.

出版信息

Front Oral Biol. 2012;16:32-51. doi: 10.1159/000337523. Epub 2012 Jun 25.

DOI:10.1159/000337523
PMID:22759668
Abstract

Vertebrate and invertebrate model organisms are essential for deciphering biological processes. One of these, the mouse, proved to be a valuable model for understanding the etiopathogenesis of a vast array of human diseases, including congenital malformations such as orofacial clefting conditions. This small mammal's usefulness in cleft lip and palate research stems not only from the striking anatomical and molecular similarities of lip and palate development between human and mouse embryos, but also from its amenability to experimental and genetic manipulation. Using some recent studies as illustrative examples, this review describes different ways of generating and exploiting mouse models to study normal and abnormal development of the lip and palate. Despite a few surmountable disadvantages of using the mouse, numerous mutants have revealed a growing number of molecular key players and have pointed at a tight and complex molecular control during each step of lip and palate development.

摘要

脊椎动物和无脊椎动物模式生物对于解读生物过程至关重要。其中之一,小鼠,已被证明是理解大量人类疾病病因发病机制的宝贵模型,包括诸如口腔颌面部裂等先天性畸形。这种小型哺乳动物在唇腭裂研究中的实用性不仅源于人类和小鼠胚胎唇腭发育在解剖学和分子层面的显著相似性,还源于其易于进行实验和基因操作。以一些近期研究为例,本综述描述了生成和利用小鼠模型来研究唇腭正常和异常发育的不同方法。尽管使用小鼠存在一些可克服的缺点,但众多突变体已揭示出越来越多的分子关键参与者,并表明在唇腭发育的每个阶段都存在紧密而复杂的分子控制。

相似文献

1
The mouse as a developmental model for cleft lip and palate research.小鼠作为唇腭裂研究的发育模型。
Front Oral Biol. 2012;16:32-51. doi: 10.1159/000337523. Epub 2012 Jun 25.
2
The etiopathogenesis of cleft lip and cleft palate: usefulness and caveats of mouse models.唇腭裂的发病机制:小鼠模型的作用与注意事项
Curr Top Dev Biol. 2008;84:37-138. doi: 10.1016/S0070-2153(08)00602-9.
3
The current understanding of cleft lip malformations.唇裂畸形的当前认识。
Facial Plast Surg. 2002 Aug;18(3):147-53. doi: 10.1055/s-2002-33061.
4
Embryology and epidemiology of cleft lip and palate.唇腭裂的胚胎学与流行病学
B-ENT. 2006;2 Suppl 4:11-9.
5
Development of the lip and palate: FGF signalling.唇腭裂的发育:成纤维细胞生长因子信号传导
Front Oral Biol. 2012;16:71-80. doi: 10.1159/000337618. Epub 2012 Jun 25.
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Observations about the normal and abnormal embryogenesis of the canine lip and palate.关于犬唇部和腭部正常及异常胚胎发生的观察。
J Craniofac Genet Dev Biol Suppl. 1986;2:241-8.
7
[Environment and genetics in the etiology of cleft lip and cleft palate with reference to the role of folic acid].[唇腭裂病因中的环境与遗传学及叶酸的作用]
Epidemiol Prev. 2000 Jan-Feb;24(1):21-7.
8
Normal and abnormal development of the lip and palate.唇腭裂的正常与异常发育
Clin Plast Surg. 1985 Oct;12(4):521-32.
9
Wnt signaling in lip and palate development.唇腭裂发育中的Wnt信号通路
Front Oral Biol. 2012;16:81-90. doi: 10.1159/000337619. Epub 2012 Jun 25.
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Future directions: molecular approaches provide insights into palatal clefting and repair.未来方向:分子方法为腭裂形成与修复提供了见解。
Front Oral Biol. 2012;16:147-54. doi: 10.1159/000337667. Epub 2012 Jun 25.

引用本文的文献

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Oral Sci Int. 2021 Jan;18(1):3-13. doi: 10.1002/osi2.1072. Epub 2020 Jun 15.
2
Transcriptomics unravels molecular players shaping dorsal lip hypertrophy in the vacuum cleaner cichlid, Gnathochromis permaxillaris.转录组学揭示了塑造真空清洁工慈鲷 Gnathochromis permaxillaris 背唇肥厚的分子机制。
BMC Genomics. 2021 Jul 5;22(1):506. doi: 10.1186/s12864-021-07775-z.
3
Spatio-Temporal Expression Pattern of Ki-67, pRB, MMP-9 and Bax in Human Secondary Palate Development.
Ki-67、pRB、MMP-9和Bax在人继发腭发育中的时空表达模式
Life (Basel). 2021 Feb 20;11(2):164. doi: 10.3390/life11020164.
4
Cleft lip and cleft palate in knockout mice is associated with alterations in epithelial-mesenchymal crosstalk.基因敲除小鼠的唇腭裂与上皮-间充质相互作用的改变有关。
Development. 2020 Apr 30;147(21):dev187369. doi: 10.1242/dev.187369.
5
Mutations in GDF11 and the extracellular antagonist, Follistatin, as a likely cause of Mendelian forms of orofacial clefting in humans.GDF11 和其细胞外拮抗剂 Follistatin 的突变可能是人类孟德尔形式的口腔面裂的原因。
Hum Mutat. 2019 Oct;40(10):1813-1825. doi: 10.1002/humu.23793. Epub 2019 Jun 18.
6
Gene expression profiling in the developing secondary palate in the absence of Tbx1 function.Tbx1 功能缺失条件下的发育中 secondary palate 中的基因表达谱。
BMC Genomics. 2018 Jun 4;19(1):429. doi: 10.1186/s12864-018-4782-y.
7
Pbx loss in cranial neural crest, unlike in epithelium, results in cleft palate only and a broader midface.颅神经嵴中 PBX 的缺失,与上皮细胞不同,只会导致腭裂,并且中面部更宽。
J Anat. 2018 Aug;233(2):222-242. doi: 10.1111/joa.12821. Epub 2018 May 23.
8
Genes and microRNAs associated with mouse cleft palate: A systematic review and bioinformatics analysis.与小鼠腭裂相关的基因和微小RNA:系统评价与生物信息学分析
Mech Dev. 2018 Apr;150:21-27. doi: 10.1016/j.mod.2018.02.003. Epub 2018 Feb 21.
9
Bone regeneration using composite non-demineralized xenogenic dentin with beta-tricalcium phosphate in experimental alveolar cleft repair in a rabbit model.使用复合非脱矿异种牙本质与β-磷酸三钙在兔牙槽裂修复实验中进行骨再生。
J Transl Med. 2017 Dec 23;15(1):263. doi: 10.1186/s12967-017-1369-3.
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Sonic hedgehog regulation of promotes cranial neural crest mesenchyme proliferation and is disrupted in cleft lip morphogenesis.音猬因子对促进颅神经嵴间充质增殖的调节作用在唇裂形态发生过程中受到破坏。
Development. 2017 Jun 1;144(11):2082-2091. doi: 10.1242/dev.149930. Epub 2017 May 15.