IOVS
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Crow, J. M.
Right arrow Articles by Johnson, R. G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Crow, J. M.
Right arrow Articles by Johnson, R. G.

Investigative Ophthalmology & Visual Science, Vol 35, 3332-3341, Copyright © 1994 by Association for Research in Vision and Ophthalmology


ARTICLES AND REPORTS

Micromolar levels of intracellular calcium reduce gap junctional permeability in lens cultures

JM Crow, MM Atkinson and RG Johnson
Department of Genetics and Cell Biology, University of Minnesota, St. Paul.

PURPOSE. To investigate in bovine and embryonic chicken lens cultures the effects of elevated intracellular calcium on the permeability of gap junctions. To determine the changes in intracellular calcium using fura-2. To detect any changes in the phosphorylation of connexin43 after ionophore treatment. METHODS. Lucifer yellow was micro-injected into individual cells, and dye spread to neighboring cells was evaluated. Intracellular calcium levels were measured using the calcium indicator, fura-2. Cultures were also labeled with 32P-orthophosphate followed by immunoprecipitation with antibodies specific for the gap junction protein, connexin43. RESULTS. Bovine lens cultures incubated in the presence of either A23187 or ionomycin showed a reduction in intercellular dye transfer. The intracellular calcium concentrations in bovine cells were increased from a mean value of 0.11 +/- .009 microM in the controls to a mean of 0.40 +/- .073 microM with ionomycin treatment. Subsequent addition of EGTA to the medium decreased the intracellular calcium concentrations to a mean of 0.26 +/- .113 microM and reversed the inhibition of dye spread found with ionomycin. With ionomycin in the medium, the phosphorylated form of connexin43 was not as prominent as in the controls. In contrast, these same treatments had no detectable effect on junctional permeability in the embryonic chicken lens cultures. Dye spread was equally extensive and rapid under control and ionophore conditions, even though fura studies showed an elevation in intracellular calcium levels. CONCLUSIONS. In the bovine cultures, physiologically relevant changes in the levels of cytoplasmic calcium markedly reduced dye transfer. The increase in cytoplasmic calcium was correlated with a change in the phosphorylation level of connexin43. The regulation of junctional communication in the chick lens cultures appears to differ significantly from that in the bovine system.


This article has been cited by other articles:


Home page
Am. J. Physiol. Cell Physiol.Home page
M. M. Lurtz and C. F. Louis
Intracellular calcium regulation of connexin43
Am J Physiol Cell Physiol, December 1, 2007; 293(6): C1806 - C1813.
[Abstract] [Full Text] [PDF]


Home page
IOVSHome page
M. M. Lurtz and C. F. Louis
Purinergic Receptor Mediated Regulation of Lens Connexin43
Invest. Ophthalmol. Vis. Sci., September 1, 2007; 48(9): 4177 - 4186.
[Abstract] [Full Text] [PDF]


Home page
Exp Biol MedHome page
R. Huang, F. Shi, T. Lei, Y. Song, C. L. Hughes, and G. Liu
Effect of the Isoflavone Genistein Against Galactose-Induced Cataracts in Rats
Exp Biol Med, January 1, 2007; 232(1): 118 - 125.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
M. M. Lurtz and C. F. Louis
Calmodulin and protein kinase C regulate gap junctional coupling in lens epithelial cells
Am J Physiol Cell Physiol, December 1, 2003; 285(6): C1475 - C1482.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
G. C. Churchill, M. M. Lurtz, and C. F. Louis
Ca2+ regulation of gap junctional coupling in lens epithelial cells
Am J Physiol Cell Physiol, September 1, 2001; 281(3): C972 - C981.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
C. H. George, J. M. Kendall, A. K. Campbell, and W. H. Evans
Connexin-Aequorin Chimerae Report Cytoplasmic Calcium Environments along Trafficking Pathways Leading to Gap Junction Biogenesis in Living COS-7 Cells
J. Biol. Chem., November 6, 1998; 273(45): 29822 - 29829.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
G. Churchill, M. Atkinson, and C. Louis
Mechanical stimulation initiates cell-to-cell calcium signaling in ovine lens epithelial cells
J. Cell Sci., January 2, 1996; 109(2): 355 - 365.
[Abstract] [PDF]


Home page
J. Biol. Chem.Home page
C. Peracchia, A. Sotkis, X. G. Wang, L. L. Peracchia, and A. Persechini
Calmodulin Directly Gates Gap Junction Channels
J. Biol. Chem., August 18, 2000; 275(34): 26220 - 26224.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
A. Baruch, D. Greenbaum, E. T. Levy, P. A. Nielsen, N. B. Gilula, N. M. Kumar, and M. Bogyo
Defining a Link between Gap Junction Communication, Proteolysis, and Cataract Formation
J. Biol. Chem., July 27, 2001; 276(31): 28999 - 29006.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1994 by the Association for Research in Vision and Ophthalmology