Tight Junction Dynamics in the Frog Urinary Bladder

References

• Anderson J. M., Bakta M. S., Fanning A. S. The structure and regulation of tight junctions. Cum Opin. Cell Biol. 1993; 5: 772–778
   PubMed Web of Science ®Google Scholar
• Balda M. S., González-Mariscal L., Contreras R. G., Macias-Silva M., ToiTes-Marquez M. E., Garcia Sainz J. A., Cereijido M. Assembly and sealing of tight junctions: Possible participation of G-proteins, phospholipase C. protein kinase C and calmodulin. J. Membr. Biol. 1991; 122: 193–202
   PubMed Web of Science ®Google Scholar
• Balda M. S., Fallon M. B., Van Itallie C. M., Anderson J. M. Structure, regulation, and pathophysiology of tight junctions in the gastrointestinal tract. Yale J. Biol Med. 1992; 65: 725–735
   PubMed Web of Science ®Google Scholar
• Balda M. S., Gonzalez-Mariscal L., Matter K., Cereijido M., Anderson J. M. Assembly of the tight junction: The role of diacylglycerol. J. Cell Biol. 1993; 123: 293–302
   PubMed Web of Science ®Google Scholar
• Bentzel C. J., Palant C. E., Fromm M. Physiological and Pathological factors affecting the tight junctions. Tight junctions, M. Cereijido. CRC Press, Boca Raton 1991; 151–173
   Google Scholar
• Berridge M. L., Irvine R. F. Inositol phosphates and cell signalling. Nature 1989; 341: 197–205
   PubMed Web of Science ®Google Scholar
• Boiler K., Vestweber D., Kemler R. Cell-adhesion molecule uvomorulin is localized in the intermediate junction of adult intestinal epithelial cells. J. Cell. Biol. 1985; 100: 327–332
   PubMed Web of Science ®Google Scholar
• Castro J. A., Sesso A., Lacaz-Vieira F. Deposition of BaSO4 in the tight junctions of amphibian epithelia causes their opening; apical Ca2+ reverses this effect. J. Membr. Biol. 1993; 134: 15–29
   PubMed Web of Science ®Google Scholar
• Catterall W. A., Striessnig J. Receptor sites for Ca2+ channel antagonists. Trends. Pharmacol. Sci. 1992; 13: 256–262
   PubMed Web of Science ®Google Scholar
• Cereijido M. Evolution of ideas on the tight junctions. Tight junctions, M. Cereijido. CRC Press, Boca Raton 1991; 1–14
   Google Scholar
• Cereijido M., Gonzalez-Mariscal L., Avila G., Contreras R. G. Tight junctions. CRC Cm. Rev. Anat. Sci. 1988; 1: 171–192
   Google Scholar
• Cereijido M., Ponce A., Gonzalez-Mariscal L. Tight junctions and apical/basolateral polarity. J. Membr. Biol. 1989; 110: 1–9
   Web of Science ®Google Scholar
• Cereijido M., Robbins E. S., Dolan W. J., Rotunno C. A., Sabatini D. D. Polarized monolayers formed by epithelial cells on a permeable and translucent support. J. Cell Biol. 1978; 77: 853–880
   PubMed Web of Science ®Google Scholar
• Citi S. Protein kinase inhibitors prevent junction dissociation induced by low extracellular calcium in MDCK epithelial cells. J. Cell Biol. 1992; 117: 169–178
   PubMed Web of Science ®Google Scholar
• Citi S. The molecular organization of tight junctions. J. Cell Biol. 1993; 121: 485–489
   PubMed Web of Science ®Google Scholar
• Claude P. Morphological factors influencing transepithelial permeability: a model for the resistance of the zonula occludens. J. Membr. Biol. 1978; 39: 219–232
   PubMed Web of Science ®Google Scholar
• Claude P., Goodenough D. A. Fracture faces of zonulae occludentes from “tight” and “leaky” epithelia. J. Cell Biol. 1973; 58: 390–400
   PubMed Web of Science ®Google Scholar
• Contreras R. G., Miller J. H., Zamora M., Gonzalez-Mariscal L., Cereijido M. Interaction of calcium with the plasma membrane of epithelial (MDCK) cells during junction formation. Am. J. Physiol. 1992; 263: C313–C318
   PubMed Web of Science ®Google Scholar
• Desmedt L., Simaels J., Van Driessche W. Ca2+-block-able, poorly selective cation channels in the apical membrane of amphibian epithelia. UO22+ reveals two chennel types. J. Gen. Physiol. 1993; 101: 85–102
   PubMed Web of Science ®Google Scholar
• Dibona D. R. Passive intercellular pathway in amphibian epithelia. Nature New Biology 1972; 238: 179–181
   PubMedGoogle Scholar
• Duffy M. E., Hainau B., Ho S., Bentzel C. J. Regulation of epithelial tight junction permeability bv cyclic AMP. Nature 1981; 294: 451–453
   PubMed Web of Science ®Google Scholar
• Easter D. W., Wade J. B., Boyer J. L. Structural integrity of hepatocyte tight junctions. J. Cell Biol. 1983; 96: 745–749
   PubMed Web of Science ®Google Scholar
• Ellis B., Schneeberger E. E., Rabito C. A. Cellular variability in the development of tight junctions after activation of protein kinase c. Am. J. Physiol. 1992; 263: F293–F300
   Google Scholar
• Erlij D., Martinez-Palomo A. Opening of tight junctions in frog skin by hypertonic urea solutions. J. Membr. Biol. 1972; 9: 229–240
   PubMed Web of Science ®Google Scholar
• Farquhar M. G., Palade G. E. Cell junctions in amphibian skin. J. Cell Biol. 1965; 26: 263–291
   PubMed Web of Science ®Google Scholar
• Galli P., Camilli B. P., Meldolesi J. Extracellular calcium and the organization of tight junctions in pancreatic acinar cells. Exp. Cell. Res. 1976; 99: 178–183
   PubMed Web of Science ®Google Scholar
• Geiger B., Ayalon O. Cadherms. Anna. Rev. Cell Biol. 1992; 8: 307–332
   Web of Science ®Google Scholar
• Gonzales E., Kirchhausen T., Linares H., Whittembury G. Observations on the action of urea and other substances in opening the paracellular pathway in amphibian skins. How organisms regulate their internal and external environment, L. Bolts, S. Maddrell, K. Schmidt-Nielsen. Cambridge University Press, Cambridge 1978; 43–52
   Google Scholar
• Gonzalez-Mariscal L., Chavez de Ramirez B., Cereijido M. Tight junction formation in cultured epithelial cells (MDCK). J. Membr. Biol. 1985a; 86: 113–125
   Web of Science ®Google Scholar
• Gonzalez-Mariscal L., Contreras R. G., Bolivar J. J., Ponce A., Chávez de Ramirez B., Cereijido M. Role of calcium in tight junction formation between epithelial cells. Am. J. Physiol. 1990; 259: C978–C986
   Google Scholar
• Grunwald G. B. The structural and functional analysis of cadherin calcium-dependent cell adhesion molecules. Curr Opin. Cell Biol. 1993; 5: 797–805
   PubMed Web of Science ®Google Scholar
• Gumbiner B. Cell adhesion molecules in epithelia. Tight junctions, M. Cereijido. CRC Press, Boca Raton 1991; 91–104
   Google Scholar
• Gumbiner B., Simons K. A functional assay for proteins involved in establishing an epithelial occluding barrier: Identification of a uvomorulin-like polypeptide. J. Cell Biol. 1986; 102: 457–468
   PubMed Web of Science ®Google Scholar
• Gumbiner B., Stevenson B. R., Gnmaldi A. The role of the cell adhesion molecule uvomorulin in the formation and maintenance of epithelial junctional complex. J. Cell Biol. 1988; 107: 1575–1587
   PubMed Web of Science ®Google Scholar
• Hille B. Ionic channels of excitable membranes. Sinauer Associates. Inc., Sunderland, Mass 1992
   Google Scholar
• Jovov B., Lewis S. A., Crowe W. E., Berg J. R., Wills N. K. Role of intracellular Ca2+ in modulation of tight junction resistance in A6 cells. Am. J. Physiol. 1994; 266: F775–F784
   PubMed Web of Science ®Google Scholar
• Kemler R., Gossler A., Mansouri A., Vestweber D. The cell adhesion molecule uvomorulin. Morphoregulatory molecules, G. M. Edelman, B. A. Cunningham, J. P. Thiery. John Wiley & Sons, New York 1990; 41–56
   Google Scholar
• Knight D. E., Sugden D., Baker P. F. Evidence implicating protein kinase C in exocytosis from electropermeabilized bovime chromaffin cells. J. Membr. Biol. 1988; 104: 21–34
   PubMed Web of Science ®Google Scholar
• Lacaz-Vieira F. Sodium flux in the apical membrane of the toad skin: aspects of its regulation and the importance of the ionic strength of the outer solution upon the reversibility of amiloride inhibition. J. Membr. Biol. 1986; 92: 27–36
   PubMed Web of Science ®Google Scholar
• Ladino C., Schneeberger E. E., Rabito C. A., Lynch R. D. Inhibition of adenine nucleotide synthesis: effect on tight junction structure and function of clone 4 MDCK cells. Eur. J. Cell Biol 1991; 55: 217–224
   PubMed Web of Science ®Google Scholar
• Madara J. L., Dharmsathaphorn K. Occluding junction structure-function relationships in a cultured epithelial monolayer. J. Cell Biol. 1985; 101: 2124–2133
   PubMed Web of Science ®Google Scholar
• Mandel L. J., Curran P. F. Response of the frog skin to steady-state voltage clamping. I. The shunt pathway. J. Gen. Phrsiol. 1972; 59: 503–518
   PubMed Web of Science ®Google Scholar
• Marcial M. A., Carlson S. L., Madara J. L. Partitioning of paracellular conductance along the ileal crypt-villus axis: A hypothesis based on structural analysis with detailed consideration of tight junction structure-function relationships. J. Membr. Biol. 1984; 80: 59–70
   PubMed Web of Science ®Google Scholar
• Martinez-Palomo A., Erlij D. Structure of tight junctions in epithelia with different permeability. Proc. Nut. Acad. Sci. USA 1975; 72: 4487–4491
   PubMed Web of Science ®Google Scholar
• Martinez-Palomo A., Meza I., Bean G., Cereijido M. Experimental modulation of occluding junctions in a cultured transporting monolayer. J. Cell Biol. 1980; 87: 736–745
   PubMed Web of Science ®Google Scholar
• Mauger J.-P., Claret M. Calcium channels in hepatocytes. J. Hepatol. 1988; 7: 278–282
   PubMed Web of Science ®Google Scholar
• McCrea P. D., Gumbiner B. M. Purification of a 92-kDa cytoplasmic protein tightly associated with the cell-cell adhesion molecule E-cadherin (uvomorulin). Characterization and extract-ability of the protein complex from the cell cytostructure. J. Biol. Chem. 1991; 266: 4514–4520
   PubMed Web of Science ®Google Scholar
• Meldolesi J., Castiglioni G., Parma R., Nassivera N., Camilli P. Ca++ -dependent disassembly and reassembly of occluding junctions in guinea pig pancreatic acinar cells. J. Cell Biol. 1978; 79: 156–172
   PubMed Web of Science ®Google Scholar
• Mullin J. M., McGinn M. T. Effects of diacylghcerols on LLC-PK1 renal epithelia: Similarity to phorbol ester tumor promoters. J. Cell Biol. 1988; 134: 357–366
   Google Scholar
• Mullin J. M., O'Brien T. G. Effects of tumor promoters on LLC-PK1 renal epithelial tight junctions and transepithelial fluxes. Am. J. Physiol. 1986; 251: C587–C602
   Google Scholar
• Nathanson M. H., Gautam A., Ng O. C., Brack R., Boyer J. L. Hormonal regulation of paracellular permeability in isolated rat hepatocyte couplets. Am. J. Physiol. 1992; 262: G1079–G1086
   PubMed Web of Science ®Google Scholar
• Nathke I. S., Hinck L. E., Nelson W. J. Epithelial cell adhesion and development of cell surface polarity: possible mechanisms for modulation of cadherin function, organization and distribution. J. Cell Sci. Suppl 1993; 17: 139–145
   PubMedGoogle Scholar
• Neter J., Wasserman W. Applied linear statistical models, D. Irwin. Richard. Inc., Home wood, Illinois 1974
   Google Scholar
• Nigam S. K., Denisenko N., Rodriguez-Boulan E., Citi S. The role of phosphorilation in development of tight junctions in cultured renal epithelial (MDCK) cells. Biochem. Biophys. Res. Comm. 1991; 181: 548–553
   PubMed Web of Science ®Google Scholar
• Nishizuka Y. The molecular heterogeneity of protein kinase C and its implications for cellular regulation. Nature 1988; 334: 661–665
   PubMed Web of Science ®Google Scholar
• Ojakian G. K. Tumor promoter-induced changes in the permeability of epithelial tight junctions. Cell 1981; 23: 95–103
   PubMed Web of Science ®Google Scholar
• Pitelka D. R., Taggart B. V., Hamamoto S. T. Effects of extracellular calcium depletion on membrane topography and occluding junctions of mammarv epithelial cells in culture. The Journal of Cell Biology 1983; 96: 613–624
   PubMed Web of Science ®Google Scholar
• Rubin L. L. Endothelial cells: adhesion and tight junctions. Cun: Opin. Cell. Biol. 1992; 4: 830–833
   PubMedGoogle Scholar
• Schneeberger E. E., Lynch R. D. Structure, function, and regulation of cellular tight junctions. Am. J. Physiol. 1992; 262: L647–L661
   PubMed Web of Science ®Google Scholar
• Sedar A. W., Forte J. G. Effects of calcium depletion on the junctional complex between oxvntic cells of gastric glands. J. Cell Biol. 1964; 22: 173–188
   PubMed Web of Science ®Google Scholar
• Shell H., Kitajima Y., Yaoita H. Involvement of protein kinase C in translocation of desmoplakins from cytosol to plasma membrane during desmosome formation in human squamous cell carcinoma cells grown in low normal calcium concentration. Exp. Cell Res. 1989; 185: 176–190
   PubMed Web of Science ®Google Scholar
• Stuart R. O., Sun A., Panichas M., Hebert S. C., Brenner B. M., Nigam S. K. Critical role for intracellular calcium in tight junction biogenesis. J. Cell Physiol. 1994; 159: 423–433
   PubMed Web of Science ®Google Scholar
• Takeichi M. Cadherins: A molecular family important in selective cell-cell adhesion. Anna. Rev. Biochem. 1990; 59: 237–252
   PubMed Web of Science ®Google Scholar
• Ussing H. H., Windhager E. E. Nature of shunt path and active sodium transport path through frog skin epithelium. Acta Physiol. Scand. 1964; 61: 484–504
   PubMedGoogle Scholar
• Van Deurs B., Koehler J. K. Tight junctions in the choroid plexus epithelium. A freeze-fracture study including complementary replicas. J. Cell Biol. 1979; 80: 662–673
   PubMed Web of Science ®Google Scholar
• Van Driessche W., Zeiske W. Ca2+-sensitive, spontaneous fluctuating, cation channels in the apical membrane of the adult frog skin epithelium. Pfluegers Archiv 1985; 405: 250–259
   PubMed Web of Science ®Google Scholar
• Vestweber D., Kemler R. Identification of a putative cell adhesion domain of uvomorulin. EMBO J. 1985; 139: 3393–3398
   Google Scholar
• Wade J. B., Karnovsky M. J. Fracture faces of osmotically disrupted zonulae occludentes. J. Cell Biol. 1974; 62: 344–350
   PubMed Web of Science ®Google Scholar
• Wade J. B., Revel J., DiScala V. A. Effect of osmotic gradients on intercellular junctions of the toad bladder. Am. J. Physiol. 1973; 224: 407–415
   PubMed Web of Science ®Google Scholar
• Winkel G. K., Ferguson J. E., Takeichi M., Nuccitelli S. Activation of protein kinase C triggers premature compaction in the four-cell stage mouse embryon. Dev. Biol. 1990; 138: 1–15
   PubMed Web of Science ®Google Scholar
• Yu J., Bose R. Calcium channels in smooth muscle. Gastroenterology 1991; 100: 1448–1460
   PubMed Web of Science ®Google Scholar