Basal calcium entry in retinal pigment epithelial cells is mediated by TRPC channels

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

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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

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