|
|
|
||||
| Home Help Feedback Subscriptions Archive Search Table of Contents | |||||
Journal of Cell Science, Vol 97, Issue 4 689-704, Copyright © 1990 by Company of Biologists
JOURNAL ARTICLES |
DL Mattey, G Burdge and DR Garrod
Cancer Research Campaign Medical Oncology Unit, University of Southampton, Southampton General Hospital, UK.
The development or maturation of intercellular adhesions following their initiation has received very little attention even though this is an area of significance for a variety of in vivo processes. Using Ca2(+)-induced desmosome formation in MDCK cells as a study system it is shown that, following its initiation, desmosome formation continues for many hours. Following Ca2+ switching the major desmosomal glycoproteins, dg2/3a,b (desmocollins), accumulate progressively at the cell surface. Accumulation is first detectable within 45 min, but continues linearly for approximately 16 h, reaching a plateau at 24-32 h at 15 times the amount present in low-Ca2+ medium (LCM). Desmosomes do not increase in size during this time, but appear to become more numerous. These results suggest that cells progressively increase their desmosome-mediated adhesion over this period of time. Cycloheximide treatment shows that approximately 93% of the total dg2/3a,b accumulation is dependent upon protein synthesis after Ca2+ switching and only approximately 7% on assembly of pre-synthesised material. Thus, although triggering of desmosome formation is rapid, protein synthesis makes a major contribution to the gradual development of desmosomal adhesion in these cells. The initial assembly phase itself can be inhibited by treating cells in LCM with chloroquine, which reduces the cell surface concentration of dg2/3a,b by 40-50%. However, slow dg2/3a,b accumulation does take place in chloroquine and, if protein synthesis is permitted, desmosome formation occurs. It is suggested that when cell contacts are formed in vivo, maximisation of intercellular adhesiveness may take many hours and is dependent on the synthesis and accumulation of adhesive components.
This article has been cited by other articles:
![]() |
D. Cohen, Y. Tian, and A. Musch Par1b Promotes Hepatic-type Lumen Polarity in Madin Darby Canine Kidney Cells via Myosin II- and E-Cadherin-dependent Signaling Mol. Biol. Cell, June 1, 2007; 18(6): 2203 - 2215. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. D. Kottke, E. Delva, and A. P. Kowalczyk The desmosome: cell science lessons from human diseases. J. Cell Sci., March 1, 2006; 119(Pt 5): 797 - 806. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Yue, J. Holton, J. Clarke, J. Hyam, T Hashimoto, M. Chidgey, and D. Garrod Characterisation of a desmocollin isoform (bovine DSC3) exclusively expressed in lower layers of stratified epithelia J. Cell Sci., January 6, 1995; 108(6): 2163 - 2173. [Abstract] [PDF] |
||||
![]() |
M. Vilela, T Hashimoto, T Nishikawa, A. North, and D Garrod A simple epithelial cell line (MDCK) shows heterogeneity of desmoglein isoforms, one resembling pemphigus vulgaris antigen J. Cell Sci., January 4, 1995; 108(4): 1743 - 1750. [Abstract] [PDF] |
||||
![]() |
I. Burdett Internalisation of desmosomes and their entry into the endocytic pathway via late endosomes in MDCK cells. Possible mechanisms for the modulation of cell adhesion by desmosomes during development J. Cell Sci., January 12, 1993; 106(4): 1115 - 1130. [Abstract] [PDF] |
||||
![]() |
P. Bogner, P. Skehan, S. Kenney, E. Sainz, M. A. Akeson, and S. J. Friedman Stabilization of intercellular contacts in MDCK cells during Ca2+ deprivation. Selective effects of monocarboxylic acids on desmosomes J. Cell Sci., October 1, 1992; 103(2): 463 - 473. [Abstract] [PDF] |
||||