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细胞极性在牙发育中的研究进展

Research progress of cell polarity in tooth development
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摘要 细胞极性是指由于极性蛋白复合物之间的相互协作或排斥,使细胞骨架、细胞器以及生物大分子等呈极性分布的特性。细胞各个部分实现不同生理功能需要细胞极性蛋白及分子的精密调控。细胞极性在牙发育中发挥着重要作用,特别对于成釉细胞和成牙本质细胞的分化和功能意义重大。文章就细胞极性及相关分子和通路在牙发育中的研究进展进行综述。 The cell polarity refers to the features of polar distribution of the cytoskeleton,organelles,and biological macromolecules caused by reciprocal cooperation or repulsion among polar protein complexes.Cell polarity is required for cells to carry out a variety of physiological functions.It allows various parts of a cell to fulfill different activities,thus is crucial for tooth development,especially for ameloblast and odontoblast differentiation and function.The research progress in cell polarity and its related molecules and pathways in tooth development is reviewed in this article.
作者 徐于婵 牛好曼 郭维华 XU Yu-chan;NIU Hao-man;GUO Wei-hua(State Key Laboratory of Oral Diseases&National Clinical Research Center for Oral Diseases&Department of Pediatric Dentistry,West China School of Stomatology,Sichuan University,Chengdu 610041,China)
出处 《中国实用口腔科杂志》 CAS 2022年第3期364-369,共6页 Chinese Journal of Practical Stomatology
基金 国家自然科学基金面上项目(31971281)。
关键词 细胞极性 牙发育 成釉细胞 成牙本质细胞 cell polarity tooth development ameloblast odontoblast
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  • 1Pispa J, Jung HS, Jernvall J, et al. Cusp patterning defect in Tabby mouse teeth and its partial rescue by FGF. Dev Biol 1999;216:521-34.
  • 2Gruneberg H. Genes and genotypes affecting the teeth of the mouse. J Embryol Ex Morphol 1965;14:137-59.
  • 3Sofaer JA. Aspects of the tabby-crinkled-downless syndrome I The development of tabby teeth. J Embryol Exp Morphol 1969;22:181-205.
  • 4Sofaer JA. Short communication: The teeth of the‘Sleek’mouse Arch Oral Biol 1977,22:299-301.
  • 5Kere J, Srivastava AK, Montonen O, et al. X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein. Nat Genet 1996;13:409-16.
  • 6Ferguson BM, Brockdorff N, Formstone E, et al. Cloning of tabby, the murine homologue of the human EDA gene: evidence for a membrane associated protein with a short collagenous domain. Hum Mol Genet 1997,6:1589-94.
  • 7Srivastava AK, Pispa J, Hartung AJ, et al. The tabby phenotype is caused by mutations in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains. Proc Natl Acad Sci U S A 1997;94:13069-74.
  • 8Monreal AW, Ferguson BM, Headon D J, et al. Mutations in the human homolog of the mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia. Nat Genet 1999;22:366-9.
  • 9Tucker AS, Headon D J, Schneider P, et al. Edar/Eda interactions regulate enamel knot formation in tooth morphogenesis. Development 2000;127:4691-700.
  • 10Headon DJ, Emmal SA, Ferguson BM, et al. Gene defect in ectodermal dysplasia implicates a death domain adapter in development. Nature 2001;414:913-6.

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