|
|
|
|
Vol. 16, Issue 3, 1071-1081, March 2005
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
-Subunits Located in Neighboring Cells


* Center for Research and Advanced Studies, Department of Physiology, Biophysics, and Neurosciences, México City 07300, México;
University College of London, Institute of Ophthalmology, Department of Cell Biology, London WC1E 6BT, United Kingdom
Submitted March 29, 2004;
Revised November 5, 2004;
Accepted December 6, 2004
Monitoring Editor: Keith Mostov
The polarized distribution of Na+,K+-ATPase plays a paramount physiological role, because either directly or through coupling with co- and countertransporters, it is responsible for the net movement of, for example, glucose, amino acids, Ca2+, K+, Cl-, and CO3H- across the whole epithelium. We report here that the
-subunit is a key factor in the polarized distribution of this enzyme. 1) Madin-Darby canine kidney (MDCK) cells (epithelial from dog kidney) express the Na+,K+-ATPase over the lateral side, but not on the basal and apical domains, as if the contact with a neighboring cell were crucial for the specific membrane location of this enzyme. 2) MDCK cells cocultured with other epithelial types (derived from human, cat, dog, pig, monkey, rabbit, mouse, hamster, and rat) express the enzyme in all (100%) homotypic MDCK/MDCK borders but rarely in heterotypic ones. 3) Although MDCK cells never express Na+,K+-ATPase at contacts with Chinese hamster ovary (CHO) cells, they do when CHO cells are transfected with
1-subunit from the dog kidney (CHO-
). 4) This may be attributed to the adhesive property of the
1-subunit, because an aggregation assay using CHO (mock-transfected) and CHO-
cells shows that the expression of dog
1-subunit in the plasma membrane does increase adhesiveness. 5) This adhesiveness does not involve adherens or tight junctions. 6) Transfection of
1-subunit forces CHO-
cells to coexpress endogenous
-subunit. Together, our results indicate that MDCK cells express Na+,K+-ATPase at a given border provided the contacting cell expresses the dog
1-subunit. The cellcell interaction thus established would suffice to account for the polarized expression and positioning of Na+,K+-ATPase in epithelial cells.
Address correspondence to: Liora Shoshani (shoshani{at}fisio.cinvestav.mx).
This article has been cited by other articles:
![]() |
G. M. Mutlu, D. Machado-Aranda, J. E. Norton, A. Bellmeyer, D. Urich, R. Zhou, and D. A. Dean Electroporation-mediated Gene Transfer of the Na+,K+-ATPase Rescues Endotoxin-induced Lung Injury Am. J. Respir. Crit. Care Med., September 15, 2007; 176(6): 582 - 590. [Abstract] [Full Text] [PDF] |
||||
![]() |
W. Schoner and G. Scheiner-Bobis Endogenous and exogenous cardiac glycosides: their roles in hypertension, salt metabolism, and cell growth Am J Physiol Cell Physiol, August 1, 2007; 293(2): C509 - C536. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. D. Laughery, R. J. Clifford, Y. Chi, and J. H. Kaplan Selective basolateral localization of overexpressed Na-K-ATPase beta1- and beta2- subunits is disrupted by butryate treatment of MDCK cells Am J Physiol Renal Physiol, June 1, 2007; 292(6): F1718 - F1725. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. M. Paul, M. J. Palladino, and G. J. Beitel A pump-independent function of the Na,K-ATPase is required for epithelial junction function and tracheal tube-size control Development, January 1, 2007; 134(1): 147 - 155. [Abstract] [Full Text] [PDF] |
||||
![]() |
O. Vagin, E. Tokhtaeva, and G. Sachs The Role of the beta1 Subunit of the Na,K-ATPase and Its Glycosylation in Cell-Cell Adhesion J. Biol. Chem., December 22, 2006; 281(51): 39573 - 39587. [Abstract] [Full Text] [PDF] |
||||
![]() |
I. Larre, A. Ponce, R. Fiorentino, L. Shoshani, R. G. Contreras, and M. Cereijido Contacts and cooperation between cells depend on the hormone ouabain PNAS, July 18, 2006; 103(29): 10911 - 10916. [Abstract] [Full Text] [PDF] |
||||
![]() |
W.-N. Lian, T.-W. Wu, R.-L. Dao, Y.-J. Chen, and C.-H. Lin Deglycosylation of Na+/K+-ATPase causes the basolateral protein to undergo apical targeting in polarized hepatic cells J. Cell Sci., January 1, 2006; 119(1): 11 - 22. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. A. Deora, N. Philp, J. Hu, D. Bok, and E. Rodriguez-Boulan Mechanisms regulating tissue-specific polarity of monocarboxylate transporters and their chaperone CD147 in kidney and retinal epithelia PNAS, November 8, 2005; 102(45): 16245 - 16250. [Abstract] [Full Text] [PDF] |
||||