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PMID:15494378
Citation |
Thomas, FC, Sheth, B, Eckert, JJ, Bazzoni, G, Dejana, E and Fleming, TP (2004) Contribution of JAM-1 to epithelial differentiation and tight-junction biogenesis in the mouse preimplantation embryo. J. Cell. Sci. 117:5599-608 |
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Abstract |
We have investigated the contribution of the tight junction (TJ) transmembrane protein junction-adhesion-molecule 1 (JAM-1) to trophectoderm epithelial differentiation in the mouse embryo. JAM-1-encoding mRNA is expressed early from the embryonic genome and is detectable as protein from the eight-cell stage. Immunofluorescence confocal analysis of staged embryos and synchronized cell clusters revealed JAM-1 recruitment to cell contact sites occurred predominantly during the first hour after division to the eight-cell stage, earlier than any other TJ protein analysed to date in this model and before E-cadherin adhesion and cell polarization. During embryo compaction later in the fourth cell cycle, JAM-1 localized transiently yet precisely to the apical microvillous pole, where protein kinase Czeta (PKCzeta) and PKCdelta are also found, indicating a role in cell surface reorganization and polarization. Subsequently, in morulae and blastocysts, JAM-1 is distributed ubiquitously at cell contact sites within the embryo but is concentrated within the trophectoderm apicolateral junctional complex, a pattern resembling that of E-cadherin and nectin-2. However, treatment of embryos with anti-JAM-1-neutralizing antibodies indicated that JAM-1 did not contribute to global embryo compaction and adhesion but rather regulated the timing of blastocoel cavity formation dependent upon establishment of the trophectoderm TJ paracellular seal. |
Links |
PubMed Online version:10.1242/jcs.01424 |
Keywords |
Adherens Junctions/metabolism; Animals; Blastocyst/physiology; Cadherins/metabolism; Cell Adhesion/physiology; Cell Adhesion Molecules/genetics; Cell Adhesion Molecules/metabolism; Cell Differentiation/physiology; Cell Polarity/physiology; Down-Regulation/physiology; Embryonic Development/physiology; Epithelial Cells/cytology; Epithelial Cells/metabolism; Female; Gene Expression Regulation, Developmental/physiology; Male; Mice; Microvilli/metabolism; Microvilli/ultrastructure; RNA, Messenger/metabolism; Receptors, Cell Surface/genetics; Receptors, Cell Surface/metabolism; Tight Junctions/physiology |
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