Skip to main content
Log in

Analysis of the distribution and phosphorylation state of ZO-1 in MDCK and nonepithelial cells

  • Articles
  • Published:
The Journal of Membrane Biology Aims and scope Submit manuscript

Abstract

We have examined the distribution and extent of phosphorylation of the tight junction-associated protein ZO-1 in the epithelial MDCK cell line, and in three cell types that do not form tight junctions: S180 (sarcoma) cells, S180 cells transfected with E-cadherin (S180L), and primary cultures of astrocytes. In shortterm calcium chelation experiments on MDCK cells, removal of extracellular calcium caused cells to pull apart. However, ZO-1 remained concentrated at the plasma membrane and no change in ZO-1 phosphorylation was observed. Maintenance of MDCK cells in low calcium medium, conditions where no tight junctions are found, resulted in altered ZO-1 distribution and lower total phosphorylation of the protein. In S180 cells, ZO-1 was diffusely distributed along the entire cell surface, with concentration of the antigen in motile regions of the cell. Cell-cell contact was not a prerequisite for ZO-1 localization at the plasma membrane in this cell type, and the phosphate content of ZO-1 was found to be lower in S180 cells relative to MDCK cells. Expression of Ecadherin in S180L cells did not alter either the distribution or phosphorylation of ZO-1. In contrast to S180 cells, ZO-1 in primary cultures of astrocytes was concentrated at sites of cell-cell contact, and the phosphorylation state was the same as that in control MDCK cells. Comparison of one-dimensional proteolytic digests of 32P-labeled ZO-1 revealed the phosphorylation of two peptides in control MDCK cells that was absent in both MDCK cells grown in low calcium and in S180 cells.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Anderson, J.M., Stevenson, B.R., Jesaitis, L.A., Goodenough, D.A., Mooseker, M.S. (1988). Characterization of ZO-1, a protein component of the tight junction from mouse liver and Madin-Darby canine kidney cells. J. Cell Biol. 106:1141–1149

    Google Scholar 

  2. Balda, M.S., Gonzalez-Mariscal, L., Contreras, R.G., Macias-Silva, M., Torres-Marquez, M.E., Garcia Sainz, J.A., Cereijido, M. (1991). Assembly and sealing of tight junctions: Possible participation of G-proteins, phospholipase C, protein kinase C and calmodulin. J. Membrane Biol. 122:193–202

    Google Scholar 

  3. Bernent, W.M., Forscher, P., Mooseker, M.S. (1993). A novel cytoskeletal structure involved in purse string wound closure and cell polarity maintenance. J. Cell Biol. 121:565–578

    Google Scholar 

  4. Bentzel, C.H., Hainau, B., Ho, S., Hui, S.W., Edelman, A., Anagnostopoulos, T., Benedetti, E.L. (1980). Cytoplasmic regulation of tight junction permeability: effect of plant cytokinins. Am. J. Physiol. 239:C75-C89

    Google Scholar 

  5. Brightman, M.W., Reese, T.S. (1969). Junctions between intimately apposed cell membranes in the vertebrate brain. J. Cell Biol. 40:648–677

    Google Scholar 

  6. Cereijido, M., Robbins, E.S., Dolan, W.J., Rotunno, C.A., Sabatini, D.D. (1978). Polarized monolayers formed by epithelial cells on permeable and translucent support. J. Cell Biol. 77:853–880

    Google Scholar 

  7. Citi, S. (1993). The molecular organization of tight junctions. J. Cell Biol. 121:485–489

    Google Scholar 

  8. Citi, S. (1992). Protein kinase inhibitors prevent junction dissociation induced by low extracellular calcium in MDCK cells. J. Cell Biol. 117:169–178

    Google Scholar 

  9. Cleveland, D.W., Fischer, S.G., Kirschner, M.W., Laemmli, U.K. (1977). Peptide mapping by limited proteolysis in sodium dodecylsulfate and analysis by gel electrofocusing. J. Biol. Chem. 252:1102–1106

    Google Scholar 

  10. Duffey, M.E., Hainau, B., Ho, S., Bentzel, C.J. (1981). Regulation of epithelial tight junction permeability by cyclic AMP. Nature 294:451–453

    Google Scholar 

  11. Ellis B., Schneeberger, E.E., Rabito, C.A. (1992). Cellular variability in the development of tight junctions after activation of protein kinase C. Am. J. Physiol. 263:F293-F300

    Google Scholar 

  12. Gumbiner, B. (1990). Generation and maintenance of epithelial cell polarity. Curr. Op. Cell Biol. 2: 881–887

    Google Scholar 

  13. Gumbiner, B., Lowenkopf, T., Apatira, D. (1991). Identification of a 160-kD polypeptide that binds to the tight junction protein ZO-1. Proc. Natl. Acad. Sci. USA 88:3460–3464

    Google Scholar 

  14. Harlow, E., Lane, D. (1988). Antibodies: A Laboratory Manual. Cold Spring Harbor Laboratory Publications, Cold Spring Harbor, NY

    Google Scholar 

  15. Howarth, A.G., Hughes, M.R., Stevenson, B.R. (1992). Detection of the tight junction-associated protein ZO-1 in astrocytes and other nonepithelial cell types. Am. J. Physiol. 262:C461-C469

    Google Scholar 

  16. Itoh, M., Nagafuchi, A., Yonemura, S., Kitani-Yasuda, T., Tsukita, S., Tsukita, S. (1993). The 220-kD protein colocalizing with cadherins in non-epithelial cell is identical to ZO-1, a tight junctionassociated protein in epithelial cells: cDNA cloning and immunoelectron microscopy. J. Cell Biol. 121:491–502

    Google Scholar 

  17. Itoh, M.S., Yonemura, A., Nagafuchi, S., Tsukita, S., Tsukita, S. (1991). A 220-kD undercoat-constitutive protein: its specific localization at cadherin-based cell-cell adhesion sites. J. Cell Biol. 15:1449–1462

    Google Scholar 

  18. Jacobson, H.R. (1979). Altered permeability in the proximal tubule response to cyclic cAMP. Am. J. Physiol. 236:F71-F79

    Google Scholar 

  19. Kishimoto, A., Nishiyama, K., Nakanishi, H., Uratsuji, Y., Nomura, H., Takeyama, Y., Nishizuka, Y. (1985). Studies on the phosphorylation of myelin basic protein by protein kinase C and adenosine 3′∶5′-monophosphate-dependent protein kinase. J. Biol. Chem. 260:12492–12499

    Google Scholar 

  20. Laemmli, U.K. (1970). Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227:680–685

    PubMed  Google Scholar 

  21. Landis, D.M.D., Weinstein, L.A., Skordeles, C.J. (1990). Serum influences the differentiation of membrane structure in cultured astrocytes. Glia 3:212–221

    Google Scholar 

  22. Lillien, L.E., Sendtner, M., Rohrer, H., Hughes, S.M., Raff, M.C. (1988). Type-2 astrocyte development in rat brain cultures is initiated by a CNTF-like protein produced by type-1 astrocytes. Neuron 1:485–494

    Google Scholar 

  23. Madara, J.L. (1987). Intestinal absorptive cell tight junctions are linked to cytoskeleton. Am. J. Physiol. 253:C171-C175

    Google Scholar 

  24. Madara, J.L., Moore, R., Carlson, S. (1987). Alteration of intestinal tight junction structure and permeability by cytoskeletal contraction. Am. J. Physiol. 253:C854-C861

    Google Scholar 

  25. Martinez-Palomo, A., Meza, I., Beaty, G., Cereijido, M. (1980). Experimental modulation of occluding junctions in a cultured transporting epithelium. J. Cell Biol. 87:736–745

    Google Scholar 

  26. Mege, R.M., Matsuzaki, F., Gallin, W.J., Goldberg, J.L, Cunningham, B.A., Edelman, G.M. (1988). Construction of epithelioid sheets by transfection of mouse sarcoma cells with cDNAs for chicken cell adhesion molecules. Proc. Natl. Acad. Sci. USA 85:7274–7278

    Google Scholar 

  27. Meza, L, Ibarra, G., Sabenero, M., Martinez-Palomo, A., Cereijido, M. (1980). Occluding junctions and cytoskeletal components in a cultured transporting epithelium. J. Cell Biol. 87:746–754

    Google Scholar 

  28. Mullin, J.M., Snock, K.V., Shurina, R.D., Noe, J., George, K., Misner, L., Imaizumi, S., O'Brien, T.G. (1992). Effects of acute vs. chronic phorbol ester exposure on transepithelial permeability and epithelial morphology. J. Cell. Physiol. 152:35–47

    Google Scholar 

  29. Nelson, W.J., Veshnock, P.J. (1987). Modulation of fodrin (membrane skeleton) stability by cell-cell contact in Madin-Darby canine kidney cells. J. Cell Biol. 104:1527–1537

    Google Scholar 

  30. Nigam, S.K., Denisenko, N., Rodriguez-Boulan, E., Citi, S. (1991). The role of phosphorylation in development of tight junctions in cultured renal epithelial (MDCK) cells. Biochem. Biophys. Res. Commun. 181:548–553

    Google Scholar 

  31. Ojakian, G.K. (1981). Tumor promoters-induced changes in permeability of epithelial tight junctions. Cell 23:95–103

    Google Scholar 

  32. Pasdar, M., Nelson, W.J. (1989). Regulation of desmosome assembly in epithelial cells: kinetics of synthesis, transport, and stabilization of desmoglein I, a major protein of the membrane core domain. J. Cell Biol. 109:163–178

    Google Scholar 

  33. Pinna, L.A. (1990). Casein kinase 2: an ‘eminence grise’ in cellular regulation? Biochim. Biophys. Acta 1054:267–284

    Google Scholar 

  34. Sedar, A.W., Forte, J.G. (1964). Effects of calcium depletion on the junctional complex between oxyntic cells of gastric mucosa. J. Cell Biol. 22:173–188

    Google Scholar 

  35. Siliciano, J.D., Goodenough, D.A. (1988). Localization of the tight junction protein, ZO-1, is modulated by extracellular calcium and cell-cell contact in Madin-Darby canine kidney epithelial cells. J. Cell Biol. 107:2389–2399

    Google Scholar 

  36. Stevenson, B.R., Anderson, J.M., Bullivant, S. (1988). The epithelial tight junction: Structure, function, and preliminary biochemical characterization. Mol. Cell. Biochem. 83:129–145

    Google Scholar 

  37. Stevenson, B.R., Anderson, J.M., Braun, I.D., Mooseker, M.S. (1989). Phosphorylation of the tight junction protein ZO-1 in two strains of Madin-Darby canine kidney cells which differ in transepithelial resistance. Biochem. J. 263:597–599

    Google Scholar 

  38. Willott, E., Balda, M.S., Fanning, A.S., Jameson, B., Van Itallie, C., Anderson, J.M. (1993). The tight junction protein ZO-1 is homologous to the Drosophila discs-large tumor suppressor protein of septate junctions. Proc. Natl. Acad. Sci. USA 90:7834–7838

    Google Scholar 

  39. Zettl, K.S., Sjaastad, M.D., Riskin, P.M., Parry, G., Machen, T.E., Firestone, G.L. (1992). Glucocorticoid-induced formation of tight junctions in mouse mammary epithelial cells in vitro. Proc. Natl. Acad. Sci. USA 89:9069–9073

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

We would like to thank Cheryl Richards for her help with the cell culture and immunohistochemistry; David Begg, Gary Firestone, Vik Maraj, Manijeh Pasdar and Colin Rasmussen for helpful discussions; Jaclyn Peebles and Greg Morrison for help with graphics and photography; and Grace Martin and Bob Campenot for rat tail collagen. We are grateful to all the members of our laboratories for their friendship, advice and support. This work was supported by an Establishment Award to B.R.S. from the Alberta Heritage Foundation for Medical Research and grants to B.R.S. from the Kidney Foundation of Canada and the Medical Research Council of Canada. A.H. is funded by a Studentship from the AHFMR. K.L.S. was supported by a grant from the National Institutes of Health (DK-42799) to Gary L. Firestone. B.R.S. is a Medical Research Council of Canada and AHFMR Scholar.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Howarth, A.G., Singer, K.L. & Stevenson, B.R. Analysis of the distribution and phosphorylation state of ZO-1 in MDCK and nonepithelial cells. J. Membarin Biol. 137, 261–270 (1994). https://doi.org/10.1007/BF00232594

Download citation

  • Received:

  • Revised:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00232594

Key words

Navigation