Role of Trpc channels, Stim1 and Orai1 in PGF(2α)-induced calcium signaling in NRK fibroblasts

• Published in: Cell calcium (Edinburgh) Vol. 51; no. 1; pp. 12 - 21
• Main Authors: Almirza, W H M, Peters, P H J, van Zoelen, E J J, Theuvenet, A P R
• Format: Journal Article
• Language: English
• Published: Netherlands 01.01.2012
• Subjects: Animals; Calcium Channels - genetics; Calcium Channels - metabolism; Calcium Signaling - drug effects; Dinoprost - pharmacology; Fibroblasts - drug effects; Fibroblasts - metabolism; Gene Expression Regulation - drug effects; Gene Knockdown Techniques; Kidney - cytology; Membrane Glycoproteins - genetics; Membrane Glycoproteins - metabolism; ORAI1 Protein; Rats; Receptors, Cell Surface - metabolism; Stromal Interaction Molecule 1; TRPC Cation Channels - metabolism
• ISSN: 1532-1991
• DOI: 10.1016/j.ceca.2011.10.001

Normal rat kidney (NRK) fibroblasts exhibit growth-dependent changes in electrophysiological properties and intracellular calcium dynamics. The transition from a quiescent state to a density-arrested state results in altered calcium entry characteristics. This coincides with modulation of the expression of the genes encoding the calcium channels Trpc1, Trpc6 and Orai1, and of the intracellular calcium sensor Stim1. In the present study we have used gene selective short hairpin (sh) RNAs against these various genes to investigate their role in (a) capacitative store-operated calcium entry (SOCE); (b) non-capacitative OAG-induced receptor-operated calcium entry (ROCE); and (c) prostaglandin F(2α) (PGF(2α))-induced Ca(2+)-oscillations in NRK fibroblasts. Intracellular calcium measurements revealed that knockdown of the genes encoding Trpc1, Orai1 and Stim1 each caused a significant reduction of SOCE in NRK cells, whereas knockdown of the gene encoding Trpc6 reduced only the OAG-induced ROCE. Furthermore, our data show that knockdown of the genes encoding Trpc1, Orai1 and Stim1, but not Trpc6, substantially reduced the frequency (up to 60%) of PGF(2α)-induced Ca(2+) oscillations in NRK cells. These results indicate that in NRK cells distinct calcium channels control the processes of SOCE, ROCE and PGF(2α)-induced Ca(2+) oscillations.