A role for intracellular calcium in tight junction reassembly after ATP depletion-repletion

American Journal of Physiology - Renal Physiology

Volumn 277, Issue 4 46-4, 1999, Pages

  Ye, Jiuming ^a   Tsukamoto, Tatsuo ^a   Sun, Adam ^b   Nigam, Sanjay K ^a,c  

^a BRIGHAM AND WOMEN S HOSPITAL   (United States)

^b BROWN UNIVERSITY   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Cytoskeleton; Injury; Ischemia; Recovery; Signaling

Indexed keywords

ANIMAL CELL; ARTICLE; CALCIUM CELL LEVEL; CELL MEMBRANE PERMEABILITY; COMPLEX FORMATION; CYTOSKELETON; ISCHEMIA; NONHUMAN; PRIORITY JOURNAL; REPERFUSION INJURY; TIGHT JUNCTION;

EID: 33748400099     PISSN: 1931857X     EISSN: 15221466     Source Type: Journal    
DOI: 10.1152/ajprenal.1999.277.4.f524     Document Type: Article

References (51)

1. Balda, M. S., L. Gonzalez-Mariscal, K. Matter, M. Cereijido, and J. M. Anderson. Assembly of the tight junction: the role of diacylglycerol. J. Cell Biol. 123: 293-302, 1993.
2. Balda, M. S., J. A. Whitney, C. Flores, G. Sirenia, M. Cereijido, and K. Matter. Functional dissociation of paracellular permeability and transepithelial electrical resistance and disruption of the apical-basolateral intramembrane diffusion barrier by expression of mutant tight junction membrane protein. J. Cell Biol. 134: 1031-1049, 1996.
3. Beck, K. A., and W. J. Nelson. The spectrin-based membrane skeleton as a membrane protein-sorting machine. Am. J. Physiol. 270 (Cell Physiol. 39): C1263-C1270, 1996.
4. Bennett, V. Spectrin-based membrane skeleton: a multipotential adaptor between plasma membrane and cytoplasm. Physiol. Rev. 4: 1029-1065, 1990.
5. Citi, S., H. Sabanay, R. Jakes, B. Geiger, and J. Kendrick-Jones. Cingulin, a new peripheral component of tight junctions. Nature 333: 272-276, 1988.
6. Denker, B. M., and S. K. Nigam. Molecular structure and assembly of the tight junction. Am. J. Physiol. 274 (Renal Physiol. 43): F1-F9, 1998.
7. Denker, B. M., C. Saha, S. Khawaja, and S. K. Nigam. Involvement of a heterotrimeric G protein a subunit in tight junction biogenesis. J. Biol. Chem. 271: 25750-25753, 1996.
8. Drubin, D. G., and W. J. Nelson. Origins of cell polarity. Cell 84: 335-344, 1996.
9. Fey, E. G., K. M. Wan, and S. Penman. Epithelial cytoskeletal framework and nuclear matrix-intermediate filament scaffold: three-dimensional organization and protein composition. J. Cell Biol. 98: 1973-1984, 1984.
10. Fish, E. M., and B. A. Molitoris. Alterations in epithelial polarity and the pathogenesis of disease states. N. Engl. J. Med. 330: 1580-1588, 1994.
11. Furuse, M., K. Fujita, T. Hiiragi, K. Fujimoto, and S. Tsukita. Claudin-1 and -2: novel integral membrane proteins localizing at tight junctions with no sequence similarity to occludin. J. Cell Biol. 141: 1539-1550, 1998.
12. Furuse, M., T. Hirose, M. Itoh, A. Nagafuchi, S. Yonemura, S. Tsukita, and S. Tsukita. Occludin: a novel integral membrane protein localizing at tight junctions. J. Cell Biol. 123: 1777-1788, 1993.
13. Furuse, M., M. Itoh, T. Hirase, A. Nagafuchi, S. Yonemura, S. Tsukita, and S. Tsukita. Direct association of occludin with ZO-1 and its possible involvement in the localization of occludin at tight junctions. J. Cell Biol. 127: 1617-1626, 1994.
14. Gopalakrishnan, S., N. Raman, S. J. Atkinson, and J. A. Marrs. Rho GTPase signaling regulates tight junction assembly and protects tight junctions during ATP depletion. Am. J. Physiol. 275 (Cell Physiol. 44): C798-C8099, 1998.
15. Grynkiewicz, G., M. Poenie, and R. Y. Tsien. A new generation of calcium indicators with greatly improved fluorescence properties. J. Biol. Chem. 260: 3440-3450, 1985.
16. Gumbiner, B., T. Lowenkopf, and D. Apatira. Identification of a 160-kDa polypeptide that binds to the tight junction protein ZO-1. Proc. Natl. Acad. Sci. USA 88: 3460-3464, 1991.
17. Haskins, J., L. Gu, E. S. Wittchen, J. Hibbard, and B. R. Stevenson. ZO-3, a novel member of the MAGUK protein family found at the tight junction, interactions with ZO-1 and occludin. J. Cell Biol. 141: 199-208, 1998.
18. Hirokawa, N., and L. G. Tilney. Interactions between actin filaments and between actin filaments and membranes in quick-frozen and deeply etched hair cells of the chick ear. J. Cell Biol. 95: 249-261, 1982.
19. Itoh, M., A. Nagafuchi, S. Moroi, and S. Tsukita. Involvement of ZO-1 in cadherin-based cell adhesion through its direct binding to a catenin and actin filaments. J. Cell Biol. 138: 181-192, 1997.
20. Itoh, M., A. Nagafuchi, S. Yonemura, T. Kitani-Yasuda, S. Tsukita, and S. Tsukita. The 220-kDa protein colocalizing with cadherins in non-epithelial cells is identical to ZO-1, a tight junction-associated protein in epithelial cells: cDNA cloning and immunoelectron microscopy. J. Cell Biol. 121: 491-502, 1993.
21. Jesaitis, L. A., and D. A. Goodenough. Molecular characterization and tissue distribution of ZO-2, a tight junction protein homologous to ZO-1 and Drosophila discs-large tumor suppressor protein. J. Cell Biol. 124: 949-961, 1994.
22. Jou, T.-S., E. E. Schneeberger, and W. J. Nelson. Structural and functional regulation of tight junctions by Rho-A and Rac 1 small GTPases. J. Cell Biol. 142: 101-115, 1998.
23. Keon, B. H., S. Schfer, C. Kuhn, C. Grund, and W. W. Franke. Symplekin, a novel type of tight junction plaque protein. J. Cell Biol. 134: 1003-1018, 1996.
24. Kuznetsov, G., K. T. Bush, P. L. Zhang, and S. K. Nigam. Pertubations in maturation of secretory proteins and their association with endoplasmic reticulum chaperones in a cell culture model for epithelial ischemia. Proc. Natl. Acad. Sci. USA 93: 8584-8589, 1996.
25. Kwon, O., W. J. Nelson, R. Sibley, P. Huie, J. D. Scanding, D. Dafoe, E. Alfrey, and B. D. Myers. Backleak, tight junctions, and cell-cell adhesion in postischemic injury to the renal allograft. J. Clin. Invest. 101: 2054-2064, 1998.
26. Madara, J. L. Intestinal absorptive cell tight junctions are linked to cytoskeleton. Am. J. Physiol. 253 (Cell Physiol. 22): C171-C175, 1987.
27. Mandel, L. J., R. Bacallao, and G. Zampighi. Uncoupling of the molecular "fence" and paracellular "gate" functions in epithelial tight junctions. Nature 361: 552-555, 1993.
28. +-ATPase and E-cadherin. J. Cell Sci. 107: 3315-3324, 1994.
29. McCarthy, K. M., I. B. Skare, M. C. Stankewich, M. Furuse, S. Tsukita, R. A. Rogers, R. D. Lynch, and E. E. Schneeberger. Occludin is a functional component of the tight junction. J. Cell Sci. 109: 2287-2298, 1996.
30. Mitic, L. L., and J. M. Anderson. Molecular architecture of tight junctions. Annu. Rev. Physiol. 60: 121-142, 1998.
31. Molitoris, B. A., and W. J. Nelson. Alterations in the establishment and maintenance of epithelial cell polarity as a basis for disease processes. J. Clin. Invest. 85: 3-9, 1990.
32. +-ATPase, ankyrin, and fodrin in Madin-Darby canine kidney (MDCK) cells: implications for the biogenesis of epithelial cell polarity. J. Cell Biol. 108: 893-902, 1989.
33. Nigam, S. K., E. Rodrigues-Boulan, and R. B. Silver. Changes in intracellular calcium during the development of epithelial polarity and junctions. Proc. Natl. Acad. Sci. USA 89: 6162-6166, 1992.
34. Rodriguez-Boulan, E., and W. J. Nelson. Morphogenesis of the polarized epithelial cell phenotype. Science 245: 718-725, 1989.
35. Saitou, M., K. Fujimoto, Y. Doi, M. Itoh, T. Fujimoto, M. Furuse, H. Takano, T. Noda, and S. Tsukita. Occludin-deficient embryonic stem cells can differentiate into polarized epithelial cells bearing tight junctions. J. Cell Biol. 141: 397-408, 1998.
36. Sakakibara, A., M. Furuse, M. Saitou, Y. Ando-Akatsuka, and S. Tsukita. Possible involvement of phosphorylation of occludin in tight junction formation. J. Cell Biol. 137: 1393-1401, 1997.
37. Sheridan, A. M., J. H. Schwartz, V. M. Kroshan, A. M. Tercyak, J. Laraia, S. Masino, and W. Lieberthal. Renal mouse proximal tubular cells are more susceptible than MDCK cells to chemical anoxia. Am. J. Physiol. 265 (Renal Fluid Electrolyte Physiol. 34): F342-F350, 1993.
38. Stevenson, B. R., and D. A. Begg. Concentration-dependent effects of cytochalasin D on tight junctions and actin filaments in MDCK epithelial cells. J. Cell Sci. 107: 367-375, 1994.
39. Stevenson, B. R., J. D. Siliciano, M. S. Mooseker, and D. A. Goodenough. Identification of ZO-1: a high molecular weight polypeptide associated with the tight junction (zonula occludens) in a variety of epithelia. J. Cell Biol. 103: 755-766, 1986.
40. Stuart, R. O., and S. K. Nigam. Development of tubular nephron. Semin. Nephrol. 15: 315-326, 1995.
41. Stuart, R. O., and S. K. Nigam. Regulated assembly of tight junctions by protein kinase C. Proc. Natl. Acad. Sci. USA 92: 6072-6076, 1995.
42. Stuart, R. O., A. Sun, K. T. Bush, and S. K. Nigam. Dependence of epithelial intercellular junction biogenesis on tharpsigargin-sensitive intracellular calcium stores. J. Biol. Chem. 271: 13636-13641, 1996.
43. Stuart, R. O., A. Sun, M. Panichas, S. C. Hebert, B. M. Brenner, and S. K. Nigam. Critical role for intracellular calcium in tight junction biogenesis. J. Cell. Physiol. 159: 423-433, 1994.
44. Toshihiko Toyofuku, M. Y., K. Otsu, T. Kuzuya, M. Hori, and M. Tada. Direct association of the gap junction protein connexin-43 with ZO-1 in cardiac myocytes. J. Biol. Chem. 273: 12725-12731, 1998.
45. Tsukamoto, T., and S. K. Nigam. Tight junction proteins form large complexes and associate with the cytoskeleton in an ATP depletion model for reversible junction assembly. J. Biol. Chem. 272: 16133-16139, 1997.
46. 45a. Tsukamoto, T., and S. K. Nigam. Role of tyrosine phosphorylation in the reassembly of occludin and other tight junction proteins. Am. J. Physiol. 276 (Renal Physiol. 45): F737-F750, 1999.
47. 2+ and glycine on lipid breakdown and death of ATP-depleted MDCK cells. Kidney Int. 48: 118-128, 1995.
48. Weinberg, J. M., J. A. Davis, N. F. Roeser, and M. A. Venkatachalam. Role of increased cytosolic free calcium in the pathogenesis of rabbit tubule cell injury and protection by glycine or acidosis. J. Clin. Invest. 87: 581-590, 1991.
49. Weinberg, J. M., J. A. Davis, and M. A. Venkatachalam. Cytosolic-free calcium increases to greater than 100 micromolar in ATP-depleted proximal tubules. J. Clin. Invest. 100: 713-722, 1997.
50. Yamamoto, T., N. Harada, K. Kano, S.-I. Taya, E. Canani, Y. Matsuura, A. Mizoguchi, C. Ide, and K. Kabuchi. The ras target AF-6 interacts with ZO-1 and serves as a peripheral component of tight junctions in epithelial cells. J. Cell Biol. 139: 785-795, 1997.
51. Zhong, Y., T. Saitoh, T. Minase, N. Sawada, K. Enomoto, and M. Mori. Monoclonal antibody 7H6 reacts with a novel tight junction-associated protein distinct from ZO-1, cingulin and ZO-2. J. Cell Biol. 120: 477-483, 1993.