The long term objective of these studies is to understand the molecular structure of the tight junction so that its functional properties can be manipulated for therapeutic purposes. Tight junctions (TJ) form a continuous intercellular seal between both epithelial and endothelial cells, creating a barrier to the paracellular movement of water, solutes such as therapeutic drugs, and immune cells. The TJs barrier properties are quite variable among cell types and physiologically regulated, although the molecular basis of this remains unknown. Pathologic processes like inflammation and specific bacterial toxins alter barrier properties with significant consequences for epithelial function. Although several TJs proteins have been identified, their functions remain unknown and several more proteins remain to be identified. This lack of knowledge has greatly impeded formulation of ideas about how cellular signaling processes regulate the paracellular barrier. The barrier appears to depend on the organization of perijunctional actin.
The specific aims of this application are to define the structural organization and function of the tight junction protein ZO-1. Recent cDNA sequencing of human ZO-1 reveals it to be a member of the Membrane-Associated Guanylate Kinase protein family (MAGUK). These are multidomain proteins found at specialized sites of cell-cell contact and speculated to serve both structural and signaling roles. One MAGUK, the product of the Drosophila discs-large gene is a known tumor suppressor. We will define the sequences within ZO-1 which bind to the known TJ proteins, ZO-2 and occludin. Methods will include the yeast two-hybrid system and co-immunoprecipitation of truncated fragments of ZO-1 expressed in cultured cells through transfection techniques. Binding interactions will be correlated with sequences within ZO-1 responsible for TJ targeting in cultured cells and for inducing changes in perijunctional actin. We hypothesize that ZO-1 influences the organization of actin and this is a mechanism that regulates paracellular permeability. Cell lines used include the MDCK canine kidney and HepG2 hepatocyte and Caco-2 enterocyte human cell lines. New TJ proteins which bind to ZO-1 will be sought using yeast two-hybrid screening of a human liver cDNA library.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK045134-09
Application #
6177360
Study Section
General Medicine A Subcommittee 2 (GMA)
Program Officer
Serrano, Jose
Project Start
1992-02-01
Project End
2002-06-30
Budget Start
2000-07-01
Budget End
2002-06-30
Support Year
9
Fiscal Year
2000
Total Cost
$353,511
Indirect Cost
Name
Yale University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
082359691
City
New Haven
State
CT
Country
United States
Zip Code
06520
Van Itallie, Christina M; Mitic, Laura L; Anderson, James M (2011) Claudin-2 forms homodimers and is a component of a high molecular weight protein complex. J Biol Chem 286:3442-50
Van Itallie, Christina M; Fanning, Alan S; Holmes, Jennifer et al. (2010) Occludin is required for cytokine-induced regulation of tight junction barriers. J Cell Sci 123:2844-52
Anderson, James M; Van Itallie, Christina M (2009) Physiology and function of the tight junction. Cold Spring Harb Perspect Biol 1:a002584
Van Itallie, Christina M; Holmes, Jennifer; Bridges, Arlene et al. (2009) Claudin-2-dependent changes in noncharged solute flux are mediated by the extracellular domains and require attachment to the PDZ-scaffold. Ann N Y Acad Sci 1165:82-7
Van Itallie, Christina M; Fanning, Alan S; Bridges, Arlene et al. (2009) ZO-1 stabilizes the tight junction solute barrier through coupling to the perijunctional cytoskeleton. Mol Biol Cell 20:3930-40
Van Itallie, Christina M; Holmes, Jennifer; Bridges, Arlene et al. (2008) The density of small tight junction pores varies among cell types and is increased by expression of claudin-2. J Cell Sci 121:298-305
Van Itallie, Christina M; Betts, Laurie; Smedley 3rd, James G et al. (2008) Structure of the claudin-binding domain of Clostridium perfringens enterotoxin. J Biol Chem 283:268-74
Jovov, Biljana; Van Itallie, Christina M; Shaheen, Nicholas J et al. (2007) Claudin-18: a dominant tight junction protein in Barrett's esophagus and likely contributor to its acid resistance. Am J Physiol Gastrointest Liver Physiol 293:G1106-13
Robertson, Susan L; Smedley 3rd, James G; Singh, Usha et al. (2007) Compositional and stoichiometric analysis of Clostridium perfringens enterotoxin complexes in Caco-2 cells and claudin 4 fibroblast transfectants. Cell Microbiol 9:2734-55
Van Itallie, Christina M; Anderson, James M (2006) Claudins and epithelial paracellular transport. Annu Rev Physiol 68:403-29

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