Wimmers, Soenke and Strauss, Olaf (2007) Basal calcium entry in retinal pigment epithelial cells is mediated by TRPC channels. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 48 (12). pp. 5767-5772. ISSN 0146-0404, 1552-5783
Full text not available from this repository. (Request a copy)Abstract
PURPOSE. Ca2+ is a major regulator of cell function. In the retinal pigment epithelium (RPE), intracellular free Ca2+ concentration ([Ca2+](i)) is essential for the maintenance of normal retinal function. Therefore, accurate control of [Ca2+](i) is vital in these cells. Because Ca2+ is permanently extruded from the cytosol, RPE cells need a basal Ca2+ entry pathway that counteracts this Ca2+ efflux. The purpose of this study was to identify the molecular basis of basal Ca2+ entry into the RPE. METHODS. [Ca2+](i) was measured using Fura-2-loaded ARPE-19 cells. The expression pattern of TRPC channels was investigated by RT-PCR with RNA extracted from ARPE-19 cells and freshly isolated RPE cells from human donor eyes. RESULTS. In most cells, basal [Ca2+](i) is highly controlled by cell membranes that are only slightly permeable to Ca2+ and by the activity of Ca2+ pumps and transporters. The authors show here that RPE cells have a basal Ca2+ conductance that is dose dependently blocked by La3+. Basal [Ca2+](i) was also strongly reduced by the TRP channel blockers Gd3+, Ni2+, 2-APB, and SKF96365 and was insensitive to blockers of other Ca2+ channels. In confirmation of this pharmacologic profile, RPE cells expressed TRPC1 and TRPC4 channels, as shown by RT-PCR experiments. CONCLUSIONS. Ca2+ is needed for several permanently occurring regulatory processes in RPE cells. The Ca2+ influx pathway identified in this study is essential to define a resting basal [Ca2+](i). This resting [Ca2+](i) may contribute, for example, to basal cytokine secretion essential for the maintenance of normal retinal function.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | RECEPTOR POTENTIAL CHANNELS; OPERATED CA2+ CHANNELS; PLASMA-MEMBRANE; FUNCTIONAL EXPRESSION; SPLICE VARIANTS; MESANGIAL CELLS; CATION CHANNEL; SMOOTH-MUSCLE; RAT; GLUTAMATE; |
| Subjects: | 600 Technology > 610 Medical sciences Medicine |
| Divisions: | Medicine > Lehrstuhl für Augenheilkunde |
| Depositing User: | Dr. Gernot Deinzer |
| Date Deposited: | 25 Nov 2020 09:29 |
| Last Modified: | 25 Nov 2020 09:29 |
| URI: | https://pred.uni-regensburg.de/id/eprint/31855 |
Actions (login required)
![]() |
View Item |

