Endothelial Cell-to-Cell Junctions: Molecular Organization and Role in Vascular Homeostasis
Top Cited Papers
- 1 July 2004
- journal article
- review article
- Published by American Physiological Society in Physiological Reviews
- Vol. 84 (3) , 869-901
- https://doi.org/10.1152/physrev.00035.2003
Abstract
Intercellular junctions mediate adhesion and communication between adjoining endothelial and epithelial cells. In the endothelium, junctional complexes comprise tight junctions, adherens junctions, and gap junctions. The expression and organization of these complexes depend on the type of vessels and the permeability requirements of perfused organs. Gap junctions are communication structures, which allow the passage of small molecular weight solutes between neighboring cells. Tight junctions serve the major functional purpose of providing a “barrier” and a “fence” within the membrane, by regulating paracellular permeability and maintaining cell polarity. Adherens junctions play an important role in contact inhibition of endothelial cell growth, paracellular permeability to circulating leukocytes and solutes. In addition, they are required for a correct organization of new vessels in angiogenesis. Extensive research in the past decade has identified several molecular components of the tight and adherens junctions, including integral membrane and intracellular proteins. These proteins interact both among themselves and with other molecules. Here, we review the individual molecules of junctions and their complex network of interactions. We also emphasize how the molecular architectures and interactions may represent a mechanistic basis for the function and regulation of junctions, focusing on junction assembly and permeability regulation. Finally, we analyze in vivo studies and highlight information that specifically relates to the role of junctions in vascular endothelial cells.Keywords
This publication has 357 references indexed in Scilit:
- Molecular and functional aspects of PECAM-1/CD31Published by Elsevier ,2003
- Mice deficient in the Rac activator Tiam1 are resistant to Ras-induced skin tumoursNature, 2002
- Use of Surface Plasmon Resonance for Real-Time Analysis of the Interaction of ZO-1 and OccludinBiochemical and Biophysical Research Communications, 2001
- Mutations in the Gene Encoding Tight Junction Claudin-14 Cause Autosomal Recessive Deafness DFNB29Cell, 2001
- Junctional Adhesion Molecule (JAM) Is Phosphorylated by Protein Kinase C upon Platelet ActivationBiochemical and Biophysical Research Communications, 2000
- The SH3 domain of the tight junction protein ZO‐1 binds to a serine protein kinase that phosphorylates a region C‐terminal to this domainFEBS Letters, 1996
- Individually Distinct Ig Homology Domains in PECAM-1 Regulate Homophilic Binding and Modulate Receptor AffinityJournal of Biological Chemistry, 1996
- Identification of AF-6 and Canoe as Putative Targets for RasJournal of Biological Chemistry, 1996
- Tumor promoter-induced changes in the permeability of epithelial cell tight junctionsCell, 1981
- Morphological factors influencing transepithelial permeability: A model for the resistance of theZonula OccludensThe Journal of Membrane Biology, 1978