期刊文献+

Gap junction-mediated cell-to-cell communication in oral development and oral diseases: a concise review of research progress 被引量:8

下载PDF
导出
摘要 Homoeostasis depends on the close connection and intimate molecular exchange between extracellular, intracellular and intercellular networks. Intercellular communication is largely mediated by gap junctions(GJs), a type of specialized membrane contact composed of variable number of channels that enable direct communication between cells by allowing small molecules to pass directly into the cytoplasm of neighbouring cells. Although considerable evidence indicates that gap junctions contribute to the functions of many organs, such as the bone, intestine, kidney, heart, brain and nerve, less is known about their role in oral development and disease. In this review, the current progress in understanding the background of connexins and the functions of gap junctions in oral development and diseases is discussed. The homoeostasis of tooth and periodontal tissues, normal tooth and maxillofacial development, saliva secretion and the integrity of the oral mucosa depend on the proper function of gap junctions.Knowledge of this pattern of cell–cell communication is required for a better understanding of oral diseases. With the everincreasing understanding of connexins in oral diseases, therapeutic strategies could be developed to target these membrane channels in various oral diseases and maxillofacial dysplasia.
出处 《International Journal of Oral Science》 SCIE CAS CSCD 2020年第2期123-131,共9页 国际口腔科学杂志(英文版)
基金 supported by the National Natural Science Foundation of China(81600840,81771047 to J.X.)。
  • 相关文献

参考文献2

二级参考文献50

  • 1Aframian DJ, Amit D, David R, Shai E, Deutsch D, Honigman A, et al. (2007). Reengineering salivary gland cells to enhance protein secretion for use in developing artificial salivary gland device. Tissue Eng, 13(5): 995-1001.
  • 2Alberts B, Johnson A, Lewis J, Raft M, Roberts K, Walter P (2002). Molecular Biology of the Cell. 4th ed. New York: Garland Science.
  • 3Baum B J, Tran SD (2006). Synergy between genetic and tissue engineering: creating an artificial salivary gland. Periodonto12000, 41(1): 218-223.
  • 4Daley WP, Gulfo KM, Sequeira S J, Larsen M (2009). Identification of a mechanochemical checkpoint and negative feedback loop regulating branching morphogenesis. Dev Biol, 336(2): 169-182.
  • 5Daphna-Iken D, Shankar DB, Lawshe A, Omitz DM, Shackleford GM, MacArthur CA (1998). MMTV-Fgf8 transgenic mice develop mammary and salivary gland neoplasia and ovarian stromal hyperplasia. Oncogene, 17(21): 2711-2717.
  • 6Davies JA (2002). Do different branching epithelia use a conserved developmental mechanism? Bioessays, 24(10): 937-948.
  • 7Davis MA, Reynolds AB (2006). Blocked acinar development, E-cadherin reduction, and intraepithelial neoplasia upon ablation of p120-catenin in the mouse salivary gland. Dev Cell 10(1): 21-31.
  • 8Moerlooze L, Spencer-Dene B, Revest JM, Hajihosseini M, Rosewell I, Dickson C (2000). An important role for the IIIb isoform of fibroblast growth factor receptor 2 (FGFR2) in mesenchymal-epithelial signalling during mouse organogenesis. Development, 127(3): 483-492.
  • 9Fukuda Y, Masuda Y, Kishi J, Hashimoto Y, Hayakawa T, Nogawa H, et al. (1988). The role of interstitial collagens in cleft formation of mouse embryonic submandibular gland during initial branching. Development, 103(2): 259-267.
  • 10Gumbiner BM (2005). Regulation of cadherin-mediated adhesion in morphogenesis. Nat Rev Mol Cell Biol, 6(8): 622-634.

共引文献9

同被引文献41

引证文献8

二级引证文献5

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部