In human senile cataracts and in most animal models of cataractogenesis, cataract formation is associated with increases in both sodium and calcium inside lens fiber cells. Because both sodium and calcium are charged molecules, it is expected that their movements across lens cell membranes will depend upon the transmembrane potential across those membranes. Potassium channels are known to be important in setting the magnitude of the transmembrane potential and thus to indirectly affect the movements of both sodium and calcium. In this proposal, molecular biology, electrophysiology, and high resolution optical imaging methods are applied to epithelial and fiber cells from lenses of several species of animals. It is the intent of the proposed experiments to identify at a molecular level, all of the potassium channels that are important contributors to the resting voltage of the lens. This includes determining their primary amino acid sequence, cloning their genes, and expressing the genes in mammalian expression systems so as to characterize each in the absence of the other potassium channels which the lens possesses. In addition, by constructing fusion proteins of the channels with green fluorescence protein, localization of the channels in two natural lens preparations will be determined as well as obtaining estimates of the time required by these cells for expression of the proteins. Localization of the messenger RNA to several regions of fiber cells will also be done. It is anticipated that the information collected from these experiments will identify candidate potassium channels which might be associated with the sodium and calcium changes which occur during cataractogenesis.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY003282-21
Application #
2888104
Study Section
Visual Sciences A Study Section (VISA)
Project Start
1987-06-01
Project End
2003-06-30
Budget Start
1999-07-01
Budget End
2000-06-30
Support Year
21
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Mayo Clinic, Rochester
Department
Type
DUNS #
City
Rochester
State
MN
Country
United States
Zip Code
55905
Rae, J L; Levis, R A (2004) Fabrication of patch pipets. Curr Protoc Neurosci Chapter 6:Unit 6.3
Mathias, Richard T; Rae, James L (2004) The lens: local transport and global transparency. Exp Eye Res 78:689-98
Ou, Yijun; Strege, Peter; Miller, Steven M et al. (2003) Syntrophin gamma 2 regulates SCN5A gating by a PDZ domain-mediated interaction. J Biol Chem 278:1915-23
Rae, James L; Levis, Richard A (2002) Single-cell electroporation. Pflugers Arch 443:664-70
Rae, J L; Shepard, A R (2000) Kir2.1 Potassium channels and corneal epithelia. Curr Eye Res 20:144-52
Rae, J L; Shepard, A R (2000) Kv3.3 potassium channels in lens epithelium and corneal endothelium. Exp Eye Res 70:339-48
Rich, A; Farrugia, G; Rae, J L (1999) Effects of melatonin on ionic currents in cultured ocular tissues. Am J Physiol 276:C923-9
Shepard, A R; Rae, J L (1999) Electrically silent potassium channel subunits from human lens epithelium. Am J Physiol 277:C412-24
Shepard, A R; Rae, J L (1999) ""Microprep"" method for rapidly isolating plasmid DNAs for restriction enzyme analysis. Biotechniques 26:868-70
Shepard, A R; Rae, J L (1998) Ion transporters and receptors in cDNA libraries from lens and cornea epithelia. Curr Eye Res 17:708-19

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