Establishment of the circumferential actin filament network is a prerequisite for localization of the cadherin-catenin complex in epithelial cells

Cell Growth and Differentiation

Volumn 10, Issue 12, 1999, Pages 839-854

  Quinlan, Margaret P ^a,b   Hyatt, Janice L ^a  

^a UNIVERSITY OF TENNESSEE HEALTH SCIENCE CENTER   (United States)

^b KYOWA HAKKO KOGYO CO LTD   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ACTIN; CADHERIN; CATENIN;

ACTIN FILAMENT; ARTICLE; CELL INTERACTION; CELLULAR DISTRIBUTION; COMPLEX FORMATION; NONHUMAN; PRIORITY JOURNAL; PROTEIN TRANSPORT; REGULATORY MECHANISM;

ACTINS; ADENOVIRUS E1A PROTEINS; ANIMALS; BETA CATENIN; CADHERINS; CELL TRANSFORMATION, VIRAL; CELLS, CULTURED; CYTOCHALASINS; CYTOSKELETAL PROTEINS; EPITHELIAL CELLS; KINETICS; MICROFILAMENTS; PROTEIN BIOSYNTHESIS; RAC GTP-BINDING PROTEINS; RATS; RATS, INBRED F344; TRANS-ACTIVATORS;

ADENOVIRIDAE;

EID: 0033403506     PISSN: 10449523     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (86)

1. Eaton, S., and Simmons, K. Apical, basal, and lateral cues for epithelial polarization. Cell, 82: 5-8, 1995.
2. Gumbiner, B. M. Cell adhesion: the molecular basis of tissue architecture and morphogenesis. Cell, 84: 345-357, 1996.
3. Drubin, D. G., and Nelson, W. J. Origins of cell polarity. Cell, 84: 335-344, 1996.
4. Pawson, T., and Scott, J. D. Signaling through scaffold, anchoring and adaptor proteins. Science (Washington DC), 278: 2075-2080, 1997.
5. Aberle, H., Schwartz, H., and Kemler, R. Cadherin-catenin complex: protein interactions and their implications for cadherin function. J. Cell. Biochem., 61: 514-523, 1996.
6. Adams, C. L., and Nelson, W. J. Cytomechanics of cadherin-mediated cell-cell adhesion. Curr. Opin. Cell Biol., 10: 572-577, 1998.
7. Marrs, J. A., and Nelson, W. J. Cadherin cell adhesion molecules in differentiation and embryogenesis. Int. Rev. Cytol., 165: 159-205, 1996.
8. Yap, A. S., Briehr, W. M., and Gumbiner, B. M. Molecular and functional analysis of cadherin-based adherens junctions. Annu. Rev. Cell Dev. Biol., 13: 119-146, 1997.
9. Kintner, C. Regulation of embryonic cell adhesion by the cadherin cytoplasmic domain. Cell, 69: 225-236, 1992.
10. Nagafuchi, A., and Takeichi, M. Cell binding function of E-cadherin is regulated by the cytoplasmic domain. EMBO J., 7: 3679-3684, 1988.
11. Chen, Y. T., Stewart, D. B., and Nelson, W. J. Coupling assembly of the E-cadherin/β-catenin complex to efficient endoplasmic reticulum exit and basal-lateral membrane targeting of E-cadherin in polarized MDCK cells. J. Cell Biol., 144: 687-699, 1999.
12. Nagafuchi, A., Ishihara, S., and Tsukita, S. The roles of catenins in the cadherin-mediated cell adhesion: functional analysis of E-cadherin-α catenin fusion molecules. J. Cell Biol., 127: 235-245, 1994.
13. Rimm, D. L., Koslov, E. R., Kebriaei, P., Cianci, C. D., and Morrow, J. S. a1(E)-catenin is an actin-binding and -bundling protein mediating the attachment of F-actin to the membrane adhesion complex. Proc. Natl. Acad. Sci. USA, 92: 8813-8817, 1995.
14. Barth, A. I., Nathke, I. S., and Nelson, W. J. Cadherins, catenins and APC protein: interplay between cytoskeletal complexes and signaling pathways. Curr. Opin. Cell Biol., 9: 683-690, 1997.
15. Ben-Ze'ev, A., and Geiger, B. Differential molecular interactions of β-catenin and plakoglobin in adhesion, signaling and cancer. Curr. Opin. Cell Biol., 10: 629-639, 1998.
16. Van Aelst, L., and D'Souza-Schorey, C. Rho GTPases and signaling networks. Genes Dev., 11: 2295-2322, 1997.
17. Janmey, P. A. The cytoskeleton and cell signaling: component localization and mechanical coupling. Physiol. Rev., 78: 763-781, 1998.
18. Schmidt, A., and Hall, M. N. Signaling to the actin cytoskeleton. Annu. Rev. Cell Dev. Biol., 14: 305-338, 1998.
19. Hirano, S., Nose, A., Hatta, K., Kawakami, A., and Takeichi, M. Calcium-dependent cell-cell adhesion molecules (cadherins): subclass specificities and possible involvement of actin bundles. J. Cell. Biol., 105: 2501-2510, 1987.
20. Angres, B., Barth, A., and Nelson, W. J. Mechanism for transition from initial to stable cell-cell adhesion: kinetic analysis of E-cadherin-mediated adhesion using a quantitative adhesion assay. J. Cell Biol., 134: 549-557, 1996.
21. Jaffe, S. H., Friedlander, D. R., Matsuzaki, F., Crossin, K. L., Cunningham, B. A., and Edelman, G. M. Differential effects of the cytoplasmic domains of cell adhesion molecules on cell aggregation and sorting-out. Proc. Natl. Acad. Sci. USA, 87: 3589-3593, 1990.
22. Braga, V. M., Machesky, L. M., Hall, A., and Hotchin, N. A. The small GTPases Rho and Rac are required for the establishment of cadherin-dependent cell-cell contacts. J. Cell Biol., 137: 1421-1431, 1997.
23. Fischer, R. S., and Quinlan, M. P. Identification of a novel mechanism of regulating the adherens junction by E1A, Rad and CAFs, which contributes to tumor progression. Cell Growth Differ., 9: 905-918, 1998.
24. Hordijk, P. L., ten Klooster, J. P., van der Kammen, R. A., Michiels, F., Oomen, L. C., and Collard, J. G. Inhibition of invasion of epithelial cells by Tiam1-Rac signaling. Science (Washington DC), 278: 1464-1466, 1997.
25. Jou, T. S., and Nelson, W. J. Effects of regulated expression of mutant RhoA and Rac1 small GTPases on the development of epithelial (MDCK) cell polarity. J. Cell Biol., 142: 85-100, 1998.
26. Kuroda, S., Fukata, M., Fujii, K., Nakamura, T., Izawa, I., and Kaibuchi, K. Regulation of cell-cell adhesion of MDCK cells by Cdc42 and Rac1 small GTPases. Biochem. Biophys. Res. Commun., 240: 430-435, 1997.
27. Kuroda, S., Fukata, M., Nagawa, M., Fujii, K., Nakamura, T., Ookubo, T., Izawa, I., Nagase, T., Nomura, N., Tani, H., Shoji, I., Matsuura, Y., Yonehara, S., and Kaibuchi, K. Role of IQGAP1, a target of the small GTPases Cdc42 and Rac1, in regulation of E-cadherin-mediated cell-cell adhesion. Science (Washington DC), 281: 832-835, 1998.
28. Potempa, S., and Ridley, A. J. Activation of both MAP kinase and phosphatidylinositide 3-kinase by Ras is required for hepatocyte growth/ scatter factor-induced adherens junction disassembly. Mol. Biol. Cell, 9: 2185-2200, 1998.
29. Sander, E. E., van Delft, S., ten Klooster, J. P., Reid, T., van der Kammen, R. A., Michiels, F., and Collard, J. G. Matrix-dependent Tiam/ Rac signaling in epithelial cells promotes either cell-cell adhesion or cell migration and is regulated by phosphatidyl 3-kinase. J. Cell Biol., 143: 1385-1398, 1998.
30. Takaishi, K., Sasaki, T., Kotani, H., Nishioka, H., and Takai, Y. Regulation of cell-cell adhesion by rac and rho small G proteins in MDCK cells. J. Cell Biol., 139: 1047-1059, 1997.
31. Wojciak-Stothard, B., Entwistle, A., Garg, R., and Ridley, A. J. Regulation of TNF-α-induced reorganization of the actin cytoskeleton and cell-cell junctions by Rho, Rac and Cdc42 in human endothelial cells. J. Cell Physiol., 176: 150-165, 1998.
32. Adams, C. L., Chen, Y.-T., Smith, S. J., and Nelson, W. J. Mechanisms of epithelial cell-cell adhesion and cell compaction revealed by high-resolution tracking of E-cadherin-green fluorescent protein. J. Cell Biol., 142: 1105-1119, 1998.
33. +-ATPase in polarized epithelial cells. Science (Washington DC), 254: 847-850, 1991.
34. Fischer, R. S., and Quinlan, M. P. The C-terminus of E1A regulates tumor progression and epithelial cell differentiation. Virology, 249: 427-439, 1998.
35. Gopalakrishnan, S., and Quinlan, M. P. Modulation of E-cadherin localization in cells expressing wild-type E1A 12S or hypertransforming mutants. Cell Growth Differ., 6: 985-998, 1995.
36. Quinlan, M. P. Rac regulates the stability of the adherens junction and its components, thus affecting epithelial cell differentiation and transformation. Oncogene, 18: 6434-6442, 1999.
37. Hirschberg, K., Miller, C. M., Ellenberg, J., Presley, J. F., Siggia, E. D., Phair, R. D., and Lippincott-Schwartz, J. Kinetic analysis of secretory protein traffic and characterization of Golgi to plasma membrane transport intermediates in living cells. J. Cell Biol., 143: 1485-1503, 1998.
38. Frisch, S. M. E1A induces the expression of epithelial characteristics. J. Cell Biol., 127: 1085-1096, 1994.
39. Houweling, A., van der Elsen, P. J., and Van der Eb, A. J. Partial transformation of primary rat cells by the leftmost 4.5% fragment of adenovirus 5 DNA. Virology, 105: 537-550, 1980.
40. Montano, X., and Lane, D. P. The adenovirus E1A gene induces differentiation of F9 teratocarcinoma cells. Mol. Cell. Biol., 7: 1782-1790, 1987.
41. Quinlan, M. P., and Grodzicker, T. Adenovirus E1A 12S protein induces DNA synthesis and proliferation in primary epithelial cells in both the presence and absence of serum. J. Virol., 61: 673-682, 1987.
42. Quinlan, M. P., and Douglas, J. L. Immortalization of primary epithelial cells requires first and second exon functions of Ad5 12S. J. Virol., 66: 2020-2030, 1992.
43. Bacallao, R., Garfinkel, A., Monke, S., Zampighi, G., and Mandel, L. J. ATP depletion: a novel method to study junctional properties in epithelial tissues. I. Rearrangement of the actin cytoskeleton. J. Cell Sci., 107: 3301-3313, 1994.
44. Nathke, I. S., Hinck, L., Swedlow, J. R., Papkoff, J., and Nelson, W. J. Defining interactions and distributions of cadherin and catenin comlexes in polarized epithelial cells. J. Cell Biol., 125: 1341-1352, 1994.
45. Fischer, R. S., Zheng, Y., and Quinlan, M. P. Rac1 and extracellularly regulated kinase activation are sufficient for E1A-dependent cooperative transformation of primary epithelial cells, but progression can only be modulated by E1A or Rac1. Cell Growth Differ., 9: 209-221, 1998.
46. Douglas, J. L., Gopalakrishnan, S., and Quinlan, M. P. Modulation of transformation of primary epithelial cells by the second exon of the Ad5 E1A 12S gene. Oncogene, 6: 2093-2103, 1991.
47. Subramanian, T., La Regina, M., and Chinnadurai, G. Enhanced ras oncogene mediated cell transformation and tumorigenesis by adenovirus 2 mutants lacking the C-terminal region of E1a protein. Oncogene, 4: 415-420, 1989.
48. Boyd, J. M., Subramanian, T., Schaeper, U., La Regina, M., Bayley, S., and Chinnadurai, G. A region in the C-terminus of adenovirus 2/5 E1a protein is required for association with a cellular phosphoprotein and important for the negative modulation of T24-ras mediated transformation, tumorigenesis and metastasis. EMBO J., 12: 469-478, 1993.
49. Linder, S., Popowicz, P., Svensson, C., Marshall, H., Bondesson, M., and Akusjarvi, G. Enhanced invasive properties of rat embryo fibroblasts transformed by adenovirus E1A mutants with deletions in the carboxy-terminal exon. Oncogene, 7: 439-443, 1992.
50. Tapon, N., and Hall, A. Rho, Rac, and Cdc42 GTPases regulate the organization of the actin cytoskeleton. Curr. Opin. Cell Biol., 9: 86-92, 1997.
51. Symons, M. Rho family GTPases: the cytoskeleton and beyond. Trends Biochem. Sci., 21: 178-181, 1996.
52. Hall, A. Rho GTPases and the actin cytoskeleton. Science (Washington DC), 279: 509-513, 1998.
53. Tanaka, K., and Takai, Y. Control of reorganization of the actin cytoskeleton by Rho family small GTP-binding proteins in yeast. Curr. Opin. Cell Biol., 10: 112-116, 1998.
54. Cooper, J. A. Effects of cytochalasin and phalloidin on actin. J. Cell Biol., 105: 1473-1478, 1987.
55. +-ATPase and E-cadherin. J. Cell Sci., 107: 3315-3324, 1994.
56. Adams, C. L., Nelson, W. J., and Smith, S. J. Quantitative analysis of cadherin-catenin-actin reorganization during development of cell-cell adhesion. J. Cell Biol., 135: 1899-1911, 1996.
57. + ion medium. J. Cell Biol., 113: 881-892, 1991.
58. Harder, T., and Gerke, V. The subcellular distribution of early endosomes is affected by the annexin II2p11(2) complex. J. Cell Biol., 123: 1119-1132, 1993.
59. Ozawa, M., and Kemler, R. Correct proteolytic cleavage is required for the cell adhesive function of uvomorulin. J. Cell Biol., 111: 1645-1650, 1990.
60. Shore, E. M., and Nelson, W. J. Biosynthesis of the cell adhesion molecule uvomorulin (E-cadherin) in Madin-Darby canine kidney (MDCK) epithelial cells. J. Biol. Chem., 266: 19672-19680, 1991.
61. Ozawa, M., Ringwald, M., and Kemler, R. Uvomorulin-catenin complex formation is regulated by a specific domain in the cytoplasmic region of the cell adhesion molecule. Proc. Natl. Acad. Sci. USA, 87: 4246-4250, 1990.
62. Nusrat, A., Giry, M., Turner, J. R., Colgan, S. P., Parkos, C. A., Carnes, D., Lemichez, E., Boquet, P., and Madara, J. L. Rho protein regulates tight junctions and perijunctional actin organization in polarized epithelia. Proc. Natl. Acad. Sci. USA, 92: 10629-10633, 1995.
63. Behrens, J., von Kries, J. P., Kuhl, M., Bruhn, L., Wedlich, D., Grosschedl, R., and Birchmeier, W. Functional interaction of β-catenin with the transcription factor LEF-1. Nature (Lond.), 382: 638-642, 1996.
64. Morin, P. J., Sparks, A. B., Korinek, V., Barker, N., Clevers, H., Vogelstein, B., and Kinzler, K. W. Activation of β-catenin-Tcf signaling in colon cancer by mutations in β-catenin or APC. Science (Washington DC), 275: 1787-1790, 1997.
65. Rubinfeld, B., Robbins, P., El, G. M., Albert, I., Porfiri, E., and Polakis, P. Stabilization of β-catenin by genetic defects in melanoma cell lines. Science (Washington DC), 275: 1790-1792, 1997.
66. Yonemura, S., Itoh, M., Nagafuchi, A., and Tsukita, S. Cell-to-cell adherens junction formation and actin filament organization: similarities and differences between non-polarized fibroblasts and polarized epithelial cells. J. Cell Sci., 108: 127-142, 1995.
67. Hinck, L., Nathke, I. S., Papkoff, J., and Nelson, W. J. Dynamics of cadherin/catenin complex formation: novel protein interactions and pathways of complex assembly. J. Cell Biol., 125: 1327-1340, 1994.
68. Keller, P., and Simons, K. Post-Golgi biosynthetic trafficking. J. Cell Sci., 170: 3001-3009, 1997.
69. Faith, K. R., and Burgess, D. R. Golgi-derived vesicles from developing epithelial cells bind actin filaments and possess myosin-I as a cytoplasmically oriented peripheral membrane protein. J. Cell Biol., 120: 117-127, 1993.
70. Musch, A., Cohen, D., and Rodriguez-Boulan, E. Myosin II is involved in the production of constitutive transport vesicles from the TGN. J. Cell Biol., 138: 291-306, 1997.
71. Stow, J. L., and Heimann, K. Vesicle budding on Golgi membranes: regulation by G proteins and myosin motors. Biochim. Biophys. Acta, 1404: 161-171, 1998.
72. Valderrama, F., Babia, T., Ayala, I., Kok, J. W., Renau-Piqueras, J., and Egea, G. Actin microfilaments are essential for the cytological positioning and morphology of the Golgi complex. Eur. J. Cell Biol., 76: 9-17, 1998.
73. Sasaki, T., and Takai, Y. The Rho small G protein family-Rho-GDI system as a temporal and spatial determinant for cytoskeletal control. Biochem. Biophys. Res. Commun., 245: 641-645, 1998.
74. Wasserman, S. FH proteins as cytoskeletal organizers. Trends Cell Biol., 8: 111-115, 1998.
75. Welch, M. D., Mallavarapu, A., Rosenblatt, J., and Mitchison, T. J. Actin dynamics in vivo. Curr. Opin. Cell Biol., 9: 54-61, 1997.
76. Sun, H. Q., Kwiatkowska, K., and Yin, H. L. Actin monomer binding proteins. Curr. Opin. Cell Biol., 7: 102-110, 1995.
77. Suetsugu, S., Miki, H., and Takenawa, T. The essential role of profilin in the assembly of actin for microspike formation. EMBO J., 17: 6516-6526, 1998.
78. Ridley, A. J., Paterson, H. F., Johnston, C. L., Diekmann, D., and Hall, A. The small GTP-binding protein rac regulates growth factor-induced membrane ruffling. Cell, 70: 401-410, 1992.
79. Aspenstrom, P. Effectors for the Rho GTPases. Curr. Opin. Cell Biol., 11: 95-102, 1999.
80. Weed, S. A., Du, Y., and Parsons, J. T. Translocation of cortactin to the cell periphery is meidated by the small GTPase Rac1. J. Cell Sci., 111: 2433-2443, 1998.
81. Van Aelst, L., Joneson, T., and Bar-Sagi, D. Identification of a novel Rac1-interacting protein involved in membrane ruffling. EMBO J., 15: 3778-3786, 1996.
82. Arber, S., Barbayannis, F. A., Hanser, H., Schneider, C., Stanyon, C. A., Bernard, O., and Caroni, P. Regulation of actin dynamics through phosphorylation of cofilin by LIM-kinase. Nature (Lond.), 393: 805-809, 1998.
83. Yang, N., Higuchi, O., Ohashi, K., Nagata, K., Wada, A., Kangawa, K., Nishida, E., and Mizuno, K. Cofilin phosphorylation by LIM-kinase 1 and its role in rac-mediated actin reorganization. Nature (Lond.), 393: 809-812, 1998.
84. Kobayashi, K., Kuroda, S., Fukata, M., Nakamura, T., Nagase, T., Nomura, N., Matsuura, Y., Yoshida-Kubomura, N., Iwamatsu, A., and Kaibuchi, K. p140Sra-1 (specifically Rac1-associated protein) is a novel specific target for Rac1 small GTPase. J. Biol. Chem., 273: 291-295, 1998.
85. Pillay, I., Nakano, H., and Sharma, S. V. Radicicol inhibits tyrosine phosphorylation of mitotic src substrate Sam68 and retards subsequent exit from mitosis of src-transformed cells. Cell Growth Differ., 7: 1487-1499, 1996.
86. Herzog, M., Dreager, A., Ehler, E., and Small, J. V. In: Cell Biology: A Laboratory Handbook, Vol. 2, pp. 355-374. San Diego, CA: Academic Press, 1994.