This grant proposes to use patch-clamp recording, Ca2+ fluorometric methods, and tissue culture to study the physiology and pharmacology of epithelial cells from the ciliary body. We are proposing to make whole- cell and perforated patch recordings from pigmented and nonpigmented cells under voltage clamp and to study changes in conductance produced by substances known to have some pharmacological effect on these cells (bombesin, carbachol, vasopressin, isoproterenol, phenylephrine, ATP, VIP) or to have effects on the intraocular pressure (catecholamines, dopamine, carbonic anhydrase inhibitors, phorbol esters, forskolin). When changes in membrane conductance can be recorded, the effects of the drugs will be characterized as to their ion selectivity, voltage dependence, and mechanism of action (role of G proteins, second messengers). We are also proposing to use the fluorometric dye fura-2 to study a possible role of Ca2+ in the response of the nonpigmented ciliary body epithelial cells to pharmacological agents, both in intact ciliary processes and for cells in primary culture. Simultaneous measurements will be made of changes in Ca2+ concentration and changes in membrane conductance, to test critically the notion that Ca2+ acts as a second messenger in this tissue. We are proposing to develop a method for culturing monolayers of nonpigmented cells on permeable supports. Our goal is to produce monolayers with sufficiently high transepithelial resistances that they can be used to make measurements of ion and water flux in this tissue. If we are able to produce such monolayers, we shall use them to study transepithelial electrical parameters (open circuit voltage and closed circuit current), and the flux of ions (Na+,K+,Cl-) which are likely to be important in the secretion of the aqueous humor. We hope also to make quantitative measurements of water flux across monolayers of nonpigmented cells, to investigate the mechanisms and pharmacology of water transport in the ciliary body.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
2R01EY007568-06A1
Application #
2161582
Study Section
Visual Sciences C Study Section (VISC)
Project Start
1988-07-01
Project End
1997-06-30
Budget Start
1994-07-01
Budget End
1995-06-30
Support Year
6
Fiscal Year
1994
Total Cost
Indirect Cost
Name
University of California Los Angeles
Department
Physiology
Type
Schools of Medicine
DUNS #
119132785
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Cilluffo, M C; Esqueda, E; Farahbakhsh, N A (2000) Multiple receptor activation elicits synergistic IP formation in nonpigmented ciliary body epithelial cells. Am J Physiol Cell Physiol 279:C734-43
Cilluffo, M C; Xia, S L; Farahbakhsh, N A et al. (1998) Synergistic receptor-activated calcium increases in single nonpigmented epithelial cells. Invest Ophthalmol Vis Sci 39:1429-35
Cilluffo, M C; Farahbakhsh, N A; Fain, G L (1997) Functional and morphological differentiation of nonpigmented ciliary body epithelial cells grown on collagen rafts. In Vitro Cell Dev Biol Anim 33:546-52
Fain, G L; Farahbakhsh, N A (1989) Voltage-activated currents recorded from rabbit pigmented ciliary body epithelial cells in culture. J Physiol 418:83-103