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


     


(Investigative Ophthalmology and Visual Science. 2005;46:1393-1402.)
© 2005 by The Association for Research in Vision and Ophthalmology, Inc.
DOI:  10.1167/iovs.04-1217

This Article
Right arrow Full Text
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 ISI Web of Science
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 ISI Web of Science (16)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Varadaraj, K.
Right arrow Articles by Mathias, R. T.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Varadaraj, K.
Right arrow Articles by Mathias, R. T.

Regulation of Aquaporin Water Permeability in the Lens

Kulandaiappan Varadaraj,1 Sindhu Kumari,1 Alan Shiels,2,3 and Richard T. Mathias1

1From the Department of Physiology and Biophysics, State University of New York at Stony Brook, Stony Brook, New York; and the 2Departments of Ophthalmology and Visual Sciences and 3Genetics, Washington University, St. Louis, Missouri.

PURPOSE. To examine Ca2+- and pH-mediated regulation of water permeability of endogenously expressed aquaporin (AQP)0 in lens fiber cells and AQP1 in lens epithelial cells.

METHODS. Large, right-side-out membrane vesicles were formed from freshly isolated groups of lens fiber cells. Osmotic shrinking or swelling of these vesicles was used to determine the water permeability of endogenously expressed AQP0. The results were compared with those in similar studies of freshly isolated lens epithelial cells, which endogenously expressed AQP1, and of oocytes, which exogenously expressed AQP0.

RESULTS. In the lens or in oocytes, decreasing external pH from 7.5 to 6.5 caused a two- to fourfold increase in the water permeability of mammalian AQP0. Several lines of evidence suggest that this effect is mediated by the binding of H+ to a histidine in the first extracellular loop (His40). Lens AQP1 lacks His40 and also lacks pH sensitivity. Increasing Ca2+ caused a two- to fourfold increase in the water permeability of endogenous AQP0. The Ca2+ effect on mouse AQP0 was a 2.5-fold increase in the lens, whereas in oocytes, it was a 4-fold decrease. In either environment, the effect was mediated through calmodulin, most likely through its binding to the proximal domain of the C terminus. Lens AQP1 does not have a similar domain and does not have calcium sensitivity.

CONCLUSIONS. In either the lens or oocytes, Ca2+ and H+ appear to affect the same mechanism, probably either the open probability of the water channel, or open-channel permeability. The difference between calcium’s effects in lens versus oocytes was remarkable and is not understood. However, in the lens, Ca2+ and H+ are both increased in inner fiber cells, and so in the physiologically relevant environment, both may act to increase the water permeability of AQP0.





This article has been cited by other articles:


Home page
J. Biol. Chem.Home page
K. Kalman, K. L. Nemeth-Cahalan, A. Froger, and J. E. Hall
Phosphorylation Determines the Calmodulin-mediated Ca2+ Response and Water Permeability of AQP0
J. Biol. Chem., July 25, 2008; 283(30): 21278 - 21283.
[Abstract] [Full Text] [PDF]


Home page
IOVSHome page
N. Nishikiori, M. Osanai, H. Chiba, T. Kojima, H. Ohguro, and N. Sawada
Inhibitory Effects of Retinoic Acid Receptor Alpha Stimulants on Murine Cataractogenesis through Suppression of Deregulated Calpains
Invest. Ophthalmol. Vis. Sci., May 1, 2007; 48(5): 2224 - 2229.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
A. K. Stewart, C. E. Kurschat, D. Burns, N. Banger, R. D. Vaughan-Jones, and S. L. Alper
Transmembrane domain histidines contribute to regulation of AE2-mediated anion exchange by pH
Am J Physiol Cell Physiol, February 1, 2007; 292(2): C909 - C918.
[Abstract] [Full Text] [PDF]


Home page
IOVSHome page
J. Ruiz-Ederra and A. S. Verkman
Accelerated cataract formation and reduced lens epithelial water permeability in aquaporin-1-deficient mice.
Invest. Ophthalmol. Vis. Sci., September 1, 2006; 47(9): 3960 - 3967.
[Abstract] [Full Text] [PDF]


Home page
IOVSHome page
K. M. L. Rose, R. G. Gourdie, A. R. Prescott, R. A. Quinlan, R. K. Crouch, and K. L. Schey
The C Terminus of Lens Aquaporin 0 Interacts with the Cytoskeletal Proteins Filensin and CP49.
Invest. Ophthalmol. Vis. Sci., April 1, 2006; 47(4): 1562 - 1570.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2005 by the Association for Research in Vision and Ophthalmology