On the role of TRPC1 in control of Ca2+ influx, cell volume, and cell cycle

作者：Madsen C P; Klausen T K; Fabian A; Hansen B J; Pedersen S F; Hoffmann E K^*

来源：American Journal of Physiology - Cell Physiology, 2012, 303(6): C625-C634.

DOI：10.1152/ajpcell.00287.2011

• TRPC1
• thapsigargin
• cell cycle
• proliferation
• volume regulation
• SOCE

Madsen CP, Klausen TK, Fabian A, Hansen BJ, Pedersen SF, Hoffmann EK. On the role of TRPC1 in control of Ca2+ influx, cell volume, and cell cycle. Am J Physiol Cell Physiol 303: C625-C634, 2012. First published June 27, 2012; doi:10.1152/ajpcell.00287.2011.-Ca+ signaling plays a crucial role in control of cell cycle progression, but the understanding of the dynamics of Ca2+ influx and release of Ca2+ from intracellular stores during the cell cycle is far from complete. The aim of the present study was to investigate the role of the free extracellular Ca2+ concentration ([Ca2+](o)) in cell proliferation, the pattern of changes in the free intracellular Ca2+ concentration ([Ca2+](i)) during cell cycle progression, and the role of the transient receptor potential (TRP)C1 in these changes as well as in cell cycle progression and cell volume regulation. In Ehrlich Lettre Ascites (ELA) cells, [Ca2+](i) decreased significantly, and the thapsigargin-releasable Ca2+ pool in the intracellular stores increased in G(1) as compared with G(0). Store-depletion-operated Ca2+ entry (SOCE) and TRPC1 protein expression level were both higher in G(1) than in G(0) and S phase, in parallel with a more effective volume regulation after swelling [regulatory volume decrease (RVD)] in G(1) as compared with S phase. Furthermore, reduction of [Ca2+](o), as well as two unspecific SOCE inhibitors, 2-APB (2-aminoethyldiphenyl borinate) and SKF96365 (1-(beta-[3-(4-methoxy-phenyl)propoxyl-4-methoxyphenethyl)1H-imidazole-hydrochloride), inhibited ELA cell proliferation. Finally, Madin-Darby canine kidney cells in which TRPC1 was stably silenced [TRPC1 knockdown (TRPC1-KD) MDCK] exhibited reduced SOCE, slower RVD, and reduced cell proliferation compared with mock controls. In conclusion, in ELA cells, SOCE and TRPC1 both seem to be upregulated in G(1) as compared with S phase, concomitant with an increased rate of RVD. Furthermore, TRPC1-KD MDCK cells exhibit decreased SOCE, decreased RVD, and decreased proliferation, suggesting that, at least in certain cell types, TRPC1 is regulated during cell cycle progression and is involved in SOCE, RVD, and cell proliferation.

• 出版日期2012-9