spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search    

The fully linked HTML version of this article has now been published.
JCS ePress online publication date 20 May 2003
doi: 10.1242/jcs.00482


This Article
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
jcs.00482v1
116/13/2791    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
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 Colosetti, P.
Right arrow Articles by Cassio, D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Colosetti, P.
Right arrow Articles by Cassio, D.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

Research Article

The type 3 inositol 1,4,5-trisphosphate receptor is concentrated at the tight junction level in polarized MDCK cells


Pascal Colosetti, Richard E.A. Tunwell, Caroline Cruttwell, Jean-Pierre Arsanto, Jean-Pierre Mauger*, and Doris Cassio
* Author for correspondence (e-mail: jean-pierre.mauger{at}ibaic.u-psud.fr)

The subcellular localization of inositol 1,4,5-trisphosphate (InsP3)-induced Ca2+ signals is important for the activation of many physiological functions. In epithelial cells the spatial distribution of InsP3 receptor is restricted to specific areas, but little is known about the relationship between the receptor's distribution and cell polarity. To investigate this relationship, the best known polarized cell model, MDCK, was examined. This cell line is characterized by a strong expression of the type 3 InsP3 receptor and the subcellular localization of this receptor was followed during cell polarization using immunofluorescence and confocal analysis. In non-polarized cells, including ras transformed f3 MDCK cells, the type 3 InsP3 receptor was found to co-localize with markers of the endoplasmic reticulum in the cytoplasm. In contrast, in polarized cells, this receptor was mostly distributed at the apex of the lateral plasma membrane with the markers of tight junctions, ZO-1 and occludin. The localization of the type 3 InsP3 receptor in the vicinity of tight junctions was confirmed by immunogold electron microscopy. The culture of MDCK cells in calcium-deprived medium, led to disruption of cell polarity and receptor redistribution in the cytoplasm. Addition of calcium to these deprived cells induced the restoration of polarity and the relocalization of the receptor to the plasma membrane. MDCK cells were stably transfected with a plasmid coding the full-length mouse type 1 InsP3 receptor tagged with EGFP at the C-terminus. The EGFP-tagged type 1 receptor and the endogenous type 3 co-localized in the cytoplasm of non-polarized cells and at the tight junction level of polarized cells. Thus, the localization of InsP3 receptor in MDCK depends on polarity.


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?


This article has been cited by other articles:


Home page
J. Physiol.Home page
D. Günzel, S. Amasheh, S. Pfaffenbach, J. F. Richter, P. J. Kausalya, W. Hunziker, and M. Fromm
Claudin-16 affects transcellular Cl\#8722; secretion in MDCK cells
J. Physiol., August 1, 2009; 587(15): 3777 - 3793.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
B. E. Isakson
Localized expression of an Ins(1,4,5)P3 receptor at the myoendothelial junction selectively regulates heterocellular Ca2+ communication
J. Cell Sci., November 1, 2008; 121(21): 3664 - 3673.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
E. N. Rittmeyer, S. Daniel, S.-C. Hsu, and M. A. Osman
A dual role for IQGAP1 in regulating exocytosis
J. Cell Sci., February 1, 2008; 121(3): 391 - 403.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
L. Yang, J. Reece, S. E. Gabriel, and S. B. Shears
Apical localization of ITPK1 enhances its ability to be a modifier gene product in a murine tracheal cell model of cystic fibrosis
J. Cell Sci., April 1, 2006; 119(7): 1320 - 1328.
[Abstract] [Full Text] [PDF]


Home page
Physiol. Rev.Home page
R. Rizzuto and T. Pozzan
Microdomains of Intracellular Ca2+: Molecular Determinants and Functional Consequences
Physiol Rev, January 1, 2006; 86(1): 369 - 408.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
M. Greenough, L. Pase, I. Voskoboinik, M. J. Petris, A. W. O'Brien, and J. Camakaris
Signals regulating trafficking of Menkes (MNK; ATP7A) copper-translocating P-type ATPase in polarized MDCK cells
Am J Physiol Cell Physiol, November 1, 2004; 287(5): C1463 - C1471.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Renal Physiol.Home page
D. B. N. Lee, N. Jamgotchian, S. G. Allen, F. W. K. Kan, and I. L. Hale
Annexin A2 heterotetramer: role in tight junction assembly
Am J Physiol Renal Physiol, September 1, 2004; 287(3): F481 - F491.
[Abstract] [Full Text] [PDF]




© The Company of Biologists Ltd 2003