A. Albert and W. Large, Activation of store-operated channels by noradrenaline via protein kinase C in rabbit portal vein myocytes, The Journal of Physiology, vol.277, issue.1, pp.113-125, 2002.
DOI : 10.1113/jphysiol.2002.022574

A. Albert and W. Large, Synergism between inositol phosphates and diacylglycerol on native TRPC6-like channels in rabbit portal vein myocytes, The Journal of Physiology, vol.435, issue.3, pp.789-795, 2003.
DOI : 10.1113/jphysiol.2003.052977

N. Allbritton, T. Meyer, and L. Stryer, Range of messenger action of calcium ion and inositol 1,4,5-trisphosphate, Science, vol.258, issue.5089, pp.1812-1815, 1992.
DOI : 10.1126/science.1465619

G. Barritt, Receptor-activated Ca2+ inflow in animal cells: a variety of pathways tailored to meet different intracellular Ca2+ signalling requirements, Biochemical Journal, vol.337, issue.2, pp.153-169, 1999.
DOI : 10.1042/bj3370153

N. Basora, G. Boulay, L. Bilodeau, E. Rousseau, and M. Payet, 20-Hydroxyeicosatetraenoic Acid (20-HETE) Activates Mouse TRPC6 Channels Expressed in HEK293 Cells, Journal of Biological Chemistry, vol.278, issue.34, pp.31709-31716, 2003.
DOI : 10.1074/jbc.M304437200

M. Berridge, M. Bootman, and P. Lipp, Calcium?A life and death signal, Nature, pp.645-648, 1998.

F. Braun, L. Broad, D. Armstrong, J. Putney, and J. , Stable Activation of Single Ca2+ Release-activated Ca2+ Channels in Divalent Cation-free Solutions, Journal of Biological Chemistry, vol.276, issue.2, pp.1063-1070, 2001.
DOI : 10.1074/jbc.M008348200

C. Chapple, R. Burt, P. Andersson, P. Greengrass, M. Wyllie et al., -adrenoceptor subtypes in the human prostate, British Journal of Urology, vol.149, issue.5, pp.585-589, 1994.
DOI : 10.1111/j.1464-410X.1994.tb09188.x

URL : https://hal.archives-ouvertes.fr/hal-00576628

D. Clapham, TRP channels as cellular sensors, Nature, vol.426, issue.6966, pp.517-524, 2003.
DOI : 10.1038/nature02196

P. Delmas, N. Wanaverbecq, F. Abogadie, M. Mistry, and D. Brown, Signaling Microdomains Define the Specificity of Receptor-Mediated InsP3 Pathways in Neurons, Neuron, vol.34, issue.2, pp.209-220, 2002.
DOI : 10.1016/S0896-6273(02)00641-4

C. Forray and S. Noble, Subtype selective ??1-adrenoceptor antagonists for the treatment of benign prostatic hyperplasia, Expert Opinion on Investigational Drugs, vol.148, issue.150, pp.2073-2094, 1999.
DOI : 10.1111/j.1464-410X.1987.tb05042.x

J. Garcia, Molecular mechanisms of thrombin-induced human and bovine endothelial cell activation, J Lab Clin Med, vol.120, issue.4, pp.513-519, 1992.

M. Gerdes, T. Dang, B. Lu, M. Larsen, L. Mcbride et al., Androgenregulated proliferation and gene transcription in a prostate smooth muscle cell line (PS-1), Endocrinology, vol.137, issue.3, pp.864-872, 1996.

M. Goel, W. Sinkins, and W. Schilling, Selective Association of TRPC Channel Subunits in Rat Brain Synaptosomes, Journal of Biological Chemistry, vol.277, issue.50, pp.48303-48310, 2002.
DOI : 10.1074/jbc.M207882200

H. Gogelein, D. Dahlem, H. Englert, and H. Lang, Flufenamic acid, mefenamic acid and niflumic acid inhibit single nonselective cation channels in the rat exocrine pancreas, FEBS Letters, vol.25, issue.1, pp.79-82, 1990.
DOI : 10.1016/0014-5793(90)80977-Q

V. Golovina, Cell proliferation is associated with enhanced capacitative Ca(2þ) entry in human arterial myocytes, Am J Physiol, vol.277, issue.2, pp.343-349, 1999.

R. Gregory, G. Rychkov, and G. Barritt, Evidence that 2-aminoethyl diphenylborate is a novel inhibitor of store-operated Ca2+ channels in liver cells, and acts through a mechanism which does not involve inositol trisphosphate receptors, Biochemical Journal, vol.354, issue.2, pp.285-290, 2001.
DOI : 10.1042/bj3540285

B. Grosse, M. Kachkache, L. Mellay, V. Lieberherr, and M. , Membrane signalling and progesterone in female and male osteoblasts. I. Involvement of intracellular Ca2+, inositol trisphosphate, and diacylglycerol, but not cAMP, Journal of Cellular Biochemistry, vol.252, issue.2, pp.334-345, 2000.
DOI : 10.1002/1097-4644(20001101)79:2<334::AID-JCB160>3.0.CO;2-M

G. Grynkiewicz, M. Poenie, and R. Tsien, A new generation of Ca 2þ indicators with greatly improved fluorescence properties, J Biol Chem, vol.260, issue.6, pp.3440-3450, 1985.

C. Harteneck, T. Plant, and G. Schultz, From worm to man: three subfamilies of TRP channels, Trends in Neurosciences, vol.23, issue.4, pp.159-166, 2000.
DOI : 10.1016/S0166-2236(99)01532-5

R. Helliwell and W. Large, Alpha 1-adrenoceptor activation of a non-selective cation current in rabbit portal vein by 1,2-diacyl-sn-glycerol., The Journal of Physiology, vol.499, issue.2, pp.417-428, 1997.
DOI : 10.1113/jphysiol.1997.sp021938

T. Hofmann, A. Obukhov, M. Schaefer, C. Harteneck, T. Gudermann et al., Direct activation of human TRPC6 and TRPC3 channels by diacylglycerol, Nature, vol.397, issue.6716, pp.259-263, 1999.

T. Hofmann, M. Schaefer, G. Schultz, and T. Gudermann, Transient receptor potential channels as molecular substrates of receptor-mediated cation entry, Journal of Molecular Medicine, vol.78, issue.1, pp.14-25, 2000.
DOI : 10.1007/s001099900070

H. Hu, Q. Gu, C. Wang, C. Colton, J. Tang et al., 2-Aminoethoxydiphenyl Borate Is a Common Activator of TRPV1, TRPV2, and TRPV3, Journal of Biological Chemistry, vol.279, issue.34, pp.35741-35748, 2004.
DOI : 10.1074/jbc.M404164200

R. Inoue, T. Okada, H. Onoue, Y. Hara, S. Shimizu et al., The Transient Receptor Potential Protein Homologue TRP6 Is the Essential Component of Vascular ??1-Adrenoceptor-Activated Ca2+-Permeable Cation Channel, Circulation Research, vol.88, issue.3, pp.325-332, 2001.
DOI : 10.1161/01.RES.88.3.325

S. Jayadev, J. Petranka, S. Cheran, J. Biermann, J. Barrett et al., Reduced Capacitative Calcium Entry Correlates with Vesicle Accumulation and Apoptosis, Journal of Biological Chemistry, vol.274, issue.12, pp.8261-8268, 1999.
DOI : 10.1074/jbc.274.12.8261

S. Jung, R. Strotmann, G. Schultz, and T. Plant, TRPC6 is a candidate channel involved in receptor-stimulated cation currents in A7r5 smooth muscle cells, AJP: Cell Physiology, vol.282, issue.2, pp.347-359, 2002.
DOI : 10.1152/ajpcell.00283.2001

S. Kaplan, Benign Prostatic Hyperplasia Management???Statistical Significance May Not Translate Into Clinical Relevance, The Journal of Urology, vol.171, issue.3, pp.1207-1208, 2004.
DOI : 10.1097/01.ju.0000113724.04816.c0

A. Lepple-wienhues, C. Belka, T. Laun, A. Jekle, B. Walter et al., Stimulation of CD95 (Fas) blocks T lymphocyte calcium channels through sphingomyelinase and sphingolipids, Proceedings of the National Academy of Sciences, vol.180, issue.4, pp.13795-13800, 1999.
DOI : 10.1084/jem.180.4.1547

J. Merritt, W. Armstrong, C. Benham, T. Hallam, R. Jacob et al., SK&F 96365, a novel inhibitor of receptor-mediated calcium entry, Biochemical Journal, vol.271, issue.2, pp.515-522, 1990.
DOI : 10.1042/bj2710515

L. Missiaen, D. Smedt, H. Parys, J. Casteels, and R. , Co-activation of inositol trisphosphate induced Ca 2þ release by cytosolic Ca 2þ is loading-dependent, 1994.

A. Parekh and R. Penner, Store depletion and calcium influx, Physiol Rev, vol.77, issue.4, pp.901-930, 1997.

J. Parys, H. De-smedt, L. Missiaen, M. Bootman, I. Sienaert et al., Rat basophiliv leukemia cells as model system for inositol 1,4,5-trisphosphate receptor IV, a receptor of the type II family: functional comparison and immunological detection, Cell Calcium, vol.17, issue.4, pp.239-249, 1995.
DOI : 10.1016/0143-4160(95)90070-5

K. Pattni, T. Millard, and G. Banting, Calpain cleavage of the B isoform of Ins(1,4,5)P3 3-kinase separates the catalytic domain from the membrane anchoring domain, Biochemical Journal, vol.375, issue.3, pp.643-651, 2003.
DOI : 10.1042/bj20030505

D. Price, D. Schwinn, J. Lomasney, L. Allen, M. Caron et al., Identification, quantification, and localization of mRNA for three distinct alpha 1 adrenergic receptor subtypes in human prostate, J Urol, vol.150, issue.2, pp.546-551, 1993.

J. Putney, J. Mckay, and R. , Capacitative calcium entry channels, BioEssays, vol.273, issue.1, pp.38-46, 1999.
DOI : 10.1002/(SICI)1521-1878(199901)21:1<38::AID-BIES5>3.0.CO;2-S

M. Roudbaraki, A. Lorsignol, L. Langouche, G. Callewaert, H. Vankelecom et al., Target cells of gamma3-melanocyte-stimulating hormone detected through intracellular Ca 2þ responses in immature rat pituitary constitute a fraction of all main pituitary cell types, but mostly express multiple hormone phenotypes at the messenger ribonucleic acid level. Refractoriness to melano- cortin-3 receptor blockade in the lacto-somatotroph lineage, Endocrinology, vol.140, issue.10, pp.4874-4885, 1999.

M. Schaefer, T. Plant, A. Obukhov, T. Hofmann, T. Gudermann et al., Receptor-mediated Regulation of the Nonselective Cation Channels TRPC4 and TRPC5, Journal of Biological Chemistry, vol.275, issue.23, pp.17517-17526, 2000.
DOI : 10.1074/jbc.275.23.17517

C. Sims and N. Allbritton, Metabolism of Inositol 1,4,5-Trisphosphate and Inositol 1,3,4,5-Tetrakisphosphate by the Oocytes of Xenopus laevis, Journal of Biological Chemistry, vol.273, issue.7, pp.4052-4058, 1998.
DOI : 10.1074/jbc.273.7.4052

R. Skryma, P. Mariot, X. Bourhis, F. Coppenolle, Y. Shuba et al., current in human prostate cancer LNCaP cells: involvement in apoptosis, The Journal of Physiology, vol.90, issue.1, pp.71-83, 2000.
DOI : 10.1111/j.1469-7793.2000.00071.x

V. Sydorenko, Y. Shuba, S. Thebault, M. Roudbaraki, G. Lepage et al., Receptor-coupled, DAG-gated Ca2+-permeable cationic channels in LNCaP human prostate cancer epithelial cells, The Journal of Physiology, vol.548, issue.3, pp.823-836, 2003.
DOI : 10.1113/jphysiol.2002.036772

URL : https://hal.archives-ouvertes.fr/inserm-00139770

T. Tamaoki, H. Nomoto, I. Takahashi, Y. Kato, M. Morimoto et al., Staurosporine, a potent inhibitor of phospholipidCa++dependent protein kinase, Biochemical and Biophysical Research Communications, vol.135, issue.2, pp.397-402, 1986.
DOI : 10.1016/0006-291X(86)90008-2

Y. Tesfai, H. Brereton, and G. Barritt, A diacylglycerol-activated Ca2+ channel in PC12 cells (an adrenal chromaffin cell line) correlates with expression of the TRP-6 (transient receptor potential) protein, Biochemical Journal, vol.358, issue.3, pp.717-726, 2001.
DOI : 10.1042/bj3580717

F. Vanden-abeele, M. Roudbaraki, Y. Shuba, R. Skryma, and N. Prevarskaya, Store-operated Ca2+ Current in Prostate Cancer Epithelial Cells: ROLE OF ENDOGENOUS Ca2+ TRANSPORTER TYPE 1, Journal of Biological Chemistry, vol.278, issue.17, pp.15381-15389, 2003.
DOI : 10.1074/jbc.M212106200

F. Vanden-abeele, L. Lemonnier, S. Thebault, G. Lepage, J. Parys et al., Two Types of Store-operated Ca2+ Channels with Different Activation Modes and Molecular Origin in LNCaP Human Prostate Cancer Epithelial Cells, Journal of Biological Chemistry, vol.279, issue.29, pp.30326-30337, 2004.
DOI : 10.1074/jbc.M400106200

URL : https://hal.archives-ouvertes.fr/inserm-00139796

S. Vanlingen, J. Parys, L. Missiaen, D. Smedt, H. Wuytack et al., Distribution of inositol 1,4,5-trisphosphate receptor isoforms, SERCA isoforms and Ca2+ binding proteins in RBLm2H3 rat basophilic leukemia cells, Cell Calcium, vol.22, issue.6, pp.475-486, 1997.
DOI : 10.1016/S0143-4160(97)90075-0

S. Vanlingen, H. Sipma, D. Smet, P. Callewaert, G. Missiaen et al., Ca2+ and calmodulin differentially modulate myo-inositol 1,4,5-trisphosphate (IP3)-binding to the recombinant ligand-binding domains of the various IP3 receptor isoforms, Biochemical Journal, vol.346, issue.2, pp.275-280, 2000.
DOI : 10.1042/bj3460275

K. Vanoverberghe, P. Mariot, V. Abeele, F. Delcourt, P. Parys et al., Mechanisms of ATP-induced calcium signaling and growth arrest in human prostate cancer cells, Cell Calcium, vol.34, issue.1, pp.75-85, 2003.
DOI : 10.1016/S0143-4160(03)00024-1

G. Vazquez, J. Lievremont, J. St, J. Putney, and J. , Human Trp3 forms both inositol trisphosphate receptor-dependent and receptor-independent store-operated cation channels in DT40 avian B lymphocytes, Proceedings of the National Academy of Sciences, vol.275, issue.34, pp.9811777-11782, 2001.
DOI : 10.1074/jbc.M004666200

B. Wilson, J. Pfeiffer, A. Smith, J. Oliver, J. Oberdorf et al., Calcium-dependent Clustering of Inositol 1,4,5-Trisphosphate Receptors, Molecular Biology of the Cell, vol.9, issue.6, pp.1465-1478, 1998.
DOI : 10.1091/mbc.9.6.1465

X. Wu, G. Babnigg, and M. Villereal, Functional significance of human trp1 and trp3 in store-operated Ca(2þ) entry in HEK-293 cells, Am J Physiol Cell Physiol, vol.278, issue.3, pp.526-536, 2000.

C. Zitt, A. Obukhov, C. Strubing, A. Zobel, F. Kalkbrenner et al., Expression of TRPC3 in Chinese Hamster Ovary Cells Results in Calcium-activated Cation Currents Not Related to Store Depletion, The Journal of Cell Biology, vol.267, issue.6, pp.1333-1341, 1997.
DOI : 10.1073/pnas.90.13.6295

C. Zitt, C. Halaszovich, and A. Luckhoff, The TRP family of cation channels: probing and advancing the concepts on receptor-activated calcium entry, Progress in Neurobiology, vol.66, issue.4, pp.243-264, 2002.
DOI : 10.1016/S0301-0082(02)00002-3