|
|
|
||||
| Home Help Feedback Subscriptions Archive Search Table of Contents | |||||
Journal of Cell Science, Vol 107, Issue 6 1697-1704, Copyright © 1994 by Company of Biologists
JOURNAL ARTICLES |
H Tanihara, M Kido, S Obata, RL Heimark, M Davidson, T St John and S Suzuki
Doheny Eye Institute, University of Southern California School of Medicine, Los Angeles 90033.
Several properties of cadherin-4 and cadherin-5 were characterized by using the cDNA transfection approach. The proteins of both cadherins had a relative molecular mass of about 130 kDa and were present at the cell periphery, especially at cell-cell contact sites. These cadherins were easily digested with trypsin, and Ca2+ protected cadherin-4, but not cadherin-5, from the digestion. In immunoprecipitation, cadherin-4 co-precipitated with two major proteins of 105 kDa and 95 kDa, respectively. The 105 kDa and the 95 kDa proteins are likely to correspond to alpha- and beta-catenins. Cadherin-5 co-precipitated with only one major protein of 95 kDa, but seems to associate with the 105 kDa protein. On the other hand, plakoglobin or gamma-catenin did not co-precipitate well with either cadherin-4 or cadherin-5 in immunoprecipitation, but plakoglobin also appears to associated weakly with these cadherins. Cadherin-4 transfectants aggregated within 30 minutes in a cell aggregation assay, but cadherin-5 transfectants did not aggregate under the same conditions. Furthermore, the transfectants of chimeric cadherin-4 with cadherin-5 cytoplasmic domain showed cell aggregation activity comparable to that of wild-type cadherin-4 transfectants, whereas the transfectants of chimeric cadherin-5 with cadherin-4 cytoplasmic domain did not show appreciable cell aggregation, suggesting that the extracellular domains of cadherins, in conjunction with their cytoplasmic domains, play an important role in cell aggregation activity. These results show that cadherin-4 is very similar to the classical cadherins, whereas cadherin-5 is functionally as well as structurally distinct from classical cadherins.
This article has been cited by other articles:
![]() |
R. Kawano, N. Matsuo, H. Tanaka, M. Nasu, H. Yoshioka, and K. Shirabe Identification and Characterization of a Soluble Cadherin-7 Isoform Produced by Alternative Splicing J. Biol. Chem., November 27, 2002; 277(49): 47679 - 47685. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. G. Kevil, N. Okayama, and J. S. Alexander H2O2-mediated permeability II: importance of tyrosine phosphatase and kinase activity Am J Physiol Cell Physiol, December 1, 2001; 281(6): C1940 - C1947. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Kodama, S. Ikeda, T. Asahara, M. Kishida, and A. Kikuchi Axin Directly Interacts with Plakoglobin and Regulates Its Stability J. Biol. Chem., September 24, 1999; 274(39): 27682 - 27688. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Noria, D. B. Cowan, A. I. Gotlieb, and B. L. Langille Transient and Steady-State Effects of Shear Stress on Endothelial Cell Adherens Junctions Circ. Res., September 17, 1999; 85(6): 504 - 514. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Shimoyama, H. Takeda, S. Yoshihara, M. Kitajima, and S. Hirohashi Biochemical Characterization and Functional Analysis of Two Type II Classic Cadherins, Cadherin-6 and -14, and Comparison with E-cadherin J. Biol. Chem., April 23, 1999; 274(17): 11987 - 11994. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Pötter, C. Bergwitz, and G. Brabant The Cadherin-Catenin System: Implications for Growth and Differentiation of Endocrine Tissues Endocr. Rev., April 1, 1999; 20(2): 207 - 239. [Abstract] [Full Text] |
||||
![]() |
M. J. Pishvaian, C. M. Feltes, P. Thompson, M. J. Bussemakers, J. A. Schalken, and S. W. Byers Cadherin-11 Is Expressed in Invasive Breast Cancer Cell Lines Cancer Res., February 1, 1999; 59(4): 947 - 952. [Abstract] [Full Text] [PDF] |
||||
![]() |
A.I. Rojas and A.R. Ahmed Adhesion Receptors in Health and Disease Critical Reviews in Oral Biology & Medicine, January 1, 1999; 10(3): 337 - 358. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Gulino, E. Delachanal, E. Concord, Y. Genoux, B. Morand, M.-O. Valiron, E. Sulpice, R. Scaife, M. Alemany, and T. Vernet Alteration of Endothelial Cell Monolayer Integrity Triggers Resynthesis of Vascular Endothelium Cadherin J. Biol. Chem., November 6, 1998; 273(45): 29786 - 29793. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Shimoyama, T. Shibata, M. Kitajima, and S. Hirohashi Molecular Cloning and Characterization of a Novel Human Classic Cadherin Homologous with Mouse Muscle Cadherin J. Biol. Chem., April 17, 1998; 273(16): 10011 - 10018. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Redfield, M. T. Nieman, and K. A. Knudsen Cadherins Promote Skeletal Muscle Differentiation in Three-dimensional Cultures J. Cell Biol., September 22, 1997; 138(6): 1323 - 1331. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Shibata, Y. Shimoyama, M. Gotoh, and S. Hirohashi Identification of Human Cadherin-14, a Novel Neurally Specific Type II Cadherin, by Protein Interaction Cloning J. Biol. Chem., February 21, 1997; 272(8): 5236 - 5240. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Suzuki Protocadherins and diversity of the cadherin superfamily J. Cell Sci., January 11, 1996; 109(11): 2609 - 2611. [Abstract] [PDF] |
||||
![]() |
F. Breviario, L. Caveda, M. Corada, I. Martin-Padura, P. Navarro, J. Golay, M. Introna, D. Gulino, M. G. Lampugnani, and E. Dejana Functional Properties of Human Vascular Endothelial Cadherin (7B4/Cadherin-5), an Endothelium-Specific Cadherin Arterioscler Thromb Vasc Biol, August 1, 1995; 15(8): 1229 - 1239. [Abstract] [Full Text] |
||||
![]() |
S Obata, H Sago, N Mori, J. Rochelle, M. Seldin, M Davidson, T St John, S Taketani, and S. Suzuki Protocadherin Pcdh2 shows properties similar to, but distinct from, those of classical cadherins J. Cell Sci., January 12, 1995; 108(12): 3765 - 3773. [Abstract] [PDF] |
||||