A TRPC-like non-selective cation current activated by alpha 1-adrenoceptors in rat mesenteric artery smooth muscle cells.

[1]  M. Piascik,et al.  α1-Adrenergic Receptors: New Insights and Directions , 2001 .

[2]  D. Clapham,et al.  Formation of Novel TRPC Channels by Complex Subunit Interactions in Embryonic Brain* , 2003, Journal of Biological Chemistry.

[3]  D. Erlinge,et al.  Plasticity of TRPC expression in arterial smooth muscle: correlation with store-operated Ca2+ entry. , 2005, American journal of physiology. Cell physiology.

[4]  M. Kawai,et al.  Cs+ inhibits spontaneous Ca2+ release from sarcoplasmic reticulum of skinned cardiac myocytes. , 1998, American journal of physiology. Heart and circulatory physiology.

[5]  A. Gurney,et al.  Store-Operated Channels Mediate Ca2+ Influx and Contraction in Rat Pulmonary Artery , 2001, Circulation research.

[6]  G. Schultz,et al.  TRPC6 is a candidate channel involved in receptor-stimulated cation currents in A7r5 smooth muscle cells. , 2002, American journal of physiology. Cell physiology.

[7]  P. Mohler,et al.  Expression and relative abundance of short transient receptor potential channels in the rat renal microcirculation. , 2004, American journal of physiology. Renal physiology.

[8]  K. Yamada,et al.  Fenamates potentiate the alpha 1-adrenoceptor-activated nonselective cation channels in rabbit portal vein smooth muscle. , 1996, Japanese journal of pharmacology.

[9]  Ying Yu,et al.  Inhibition of endogenous TRP1 decreases capacitative Ca2+ entry and attenuates pulmonary artery smooth muscle cell proliferation. , 2002, American journal of physiology. Lung cellular and molecular physiology.

[10]  G. Droogmans,et al.  Exchange characteristics of the noradrenaline‐sensitive calcium store in vascular smooth muscle cells or rabbit ear artery. , 1981, The Journal of physiology.

[11]  J. Faber,et al.  Systemic α1A-adrenoceptor antagonist inhibits neointimal growth after balloon injury of rat carotid artery , 2003 .

[12]  J. Hancox,et al.  The effect of internal sodium and caesium on phasic contraction of patch‐clamped rabbit ventricular myocytes. , 1996, The Journal of physiology.

[13]  W. Large,et al.  Comparison of spontaneous and noradrenaline‐evoked non‐selective cation channels in rabbit portal vein myocytes , 2001, The Journal of physiology.

[14]  C. Garland,et al.  K+ is an endothelium-derived hyperpolarizing factor in rat arteries , 1998, Nature.

[15]  W. Large.  Receptor‐Operated Ca2+‐Permeable Nonselective Cation Channels in Vascular Smooth Muscle: A Physiologic Perspective , 2002, Journal of cardiovascular electrophysiology.

[16]  C. Romanin,et al.  Coassembly of Trp1 and Trp3 proteins generates diacylglycerol- and Ca2+-sensitive cation channels. , 2000 .

[17]  K. Muraki,et al.  Non‐selective cationic channels of smooth muscle and the mammalian homologues of Drosophila TRP , 2004, The Journal of physiology.

[18]  D. Poburko,et al.  Sequential opening of IP3-sensitive Ca2+channels and SOC during α-adrenergic activation of rabbit vena cava , 2002 .

[19]  N. Standen,et al.  Angiotensin II inhibits and alters kinetics of voltage-gated K(+) channels of rat arterial smooth muscle. , 2001, American journal of physiology. Heart and circulatory physiology.

[20]  B. Nilius,et al.  Transient receptor potential channels in endothelium: solving the calcium entry puzzle? , 2003, Endothelium : journal of endothelial cell research.

[21]  Ying Yu,et al.  PDGF stimulates pulmonary vascular smooth muscle cell proliferation by upregulating TRPC6 expression. , 2003, American journal of physiology. Cell physiology.

[22]  R. Andriantsitohaina,et al.  Mechanism of Ca2+ release and entry during contraction elicited by norepinephrine in rat resistance arteries. , 1999, American journal of physiology. Heart and circulatory physiology.

[23]  R. Inoue,et al.  Dual regulation of cation‐selective channels by muscarinic and alpha 1‐adrenergic receptors in the rabbit portal vein. , 1993, The Journal of physiology.

[24]  A. Newton,et al.  Protein kinase C: a paradigm for regulation of protein function by two membrane-targeting modules. , 1998, Biochimica et biophysica acta.

[25]  P. Langton,et al.  Potassium does not mimic EDHF in rat mesenteric arteries , 2000, British journal of pharmacology.

[26]  W. Large,et al.  Inhibitory regulation of constitutive transient receptor potential‐like cation channels in rabbit ear artery myocytes , 2004, The Journal of physiology.

[27]  G. Barritt,et al.  Receptor-activated Ca2+ inflow in animal cells: a variety of pathways tailored to meet different intracellular Ca2+ signalling requirements. , 1999, The Biochemical journal.

[28]  M. Blaustein,et al.  Na(+) entry via store-operated channels modulates Ca(2+) signaling in arterial myocytes. , 2000, American journal of physiology. Cell physiology.

[29]  T. Gudermann,et al.  Subunit composition of mammalian transient receptor potential channels in living cells , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[30]  W. Large,et al.  Properties of a constitutively active Ca2+‐permeable non‐selective cation channel in rabbit ear artery myocytes , 2003, The Journal of physiology.

[31]  W. Large,et al.  Activation of store‐operated channels by noradrenaline via protein kinase C in rabbit portal vein myocytes , 2002, The Journal of physiology.

[32]  W. Arendshorst,et al.  Calmodulin mediates norepinephrine-induced receptor-operated calcium entry in preglomerular resistance arteries. , 2005, American journal of physiology. Renal physiology.

[33]  W. Large,et al.  Synergism between inositol phosphates and diacylglycerol on native TRPC6‐like channels in rabbit portal vein myocytes , 2003, The Journal of physiology.

[34]  T. Gudermann,et al.  Direct activation of human TRPC6 and TRPC3 channels by diacylglycerol , 1999, Nature.

[35]  N. Morel,et al.  Rho‐dependent kinase is involved in agonist‐activated calcium entry in rat arteries , 2003, The Journal of physiology.

[36]  M. Nelson,et al.  Transient Receptor Potential Channels Regulate Myogenic Tone of Resistance Arteries , 2002, Circulation research.

[37]  B. Nilius,et al.  TRP channels: an overview. , 2005, Cell calcium.

[38]  David E. Clapham,et al.  TRP channels as cellular sensors , 2003, Nature.

[39]  J. Herbert,et al.  Chelerythrine is a potent and specific inhibitor of protein kinase C. , 1990, Biochemical and biophysical research communications.

[40]  H. Kennedy,et al.  Fast Ca2+ signals at mouse inner hair cell synapse: a role for Ca2+‐induced Ca2+ release , 2002, The Journal of physiology.

[41]  H. Coste,et al.  The bisindolylmaleimide GF 109203X is a potent and selective inhibitor of protein kinase C. , 1991, The Journal of biological chemistry.

[42]  A. Banes,et al.  Different alpha-adrenoceptors mediate migration of vascular smooth muscle cells and adventitial fibroblasts in vitro. , 2002, American journal of physiology. Heart and circulatory physiology.

[43]  D. Clapham,et al.  TRPC1 and TRPC5 Form a Novel Cation Channel in Mammalian Brain , 2001, Neuron.

[44]  Y. Hara,et al.  The Transient Receptor Potential Protein Homologue TRP6 Is the Essential Component of Vascular &agr;1-Adrenoceptor–Activated Ca2+-Permeable Cation Channel , 2001, Circulation research.

[45]  D. Bates,et al.  Evidence of a role for TRPC channels in VEGF-mediated increased vascular permeability in vivo. , 2004, American journal of physiology. Heart and circulatory physiology.

[46]  J. Putney,et al.  Store-operated calcium channels. , 2005, Physiological reviews.

[47]  R. Helliwell,et al.  Facilitatory effect of Ca2+ on the noradrenaline‐evoked cation current in rabbit portal vein smooth muscle cells , 1998, The Journal of physiology.

[48]  L. Shimoda,et al.  Capacitative calcium entry and TRPC channel proteins are expressed in rat distal pulmonary arterial smooth muscle. , 2004, American journal of physiology. Lung cellular and molecular physiology.

[49]  A. Gibson,et al.  The developing relationship between receptor‐operated and store‐operated calcium channels in smooth muscle , 2002, British journal of pharmacology.

[50]  A. Pries,et al.  Expression of ryanodine receptor type 3 and TRP channels in endothelial cells: comparison of in situ and cultured human endothelial cells. , 2001, Cardiovascular research.

[51]  D. Beech,et al.  TrpC1 Is a Membrane-Spanning Subunit of Store-Operated Ca2+ Channels in Native Vascular Smooth Muscle Cells , 2001, Circulation research.

[52]  J E Faber,et al.  Trophic Effect of Norepinephrine on Arterial Intima-Media and Adventitia Is Augmented by Injury and Mediated by Different &agr;1-Adrenoceptor Subtypes , 2001, Circulation research.

[53]  W A Large,et al.  Alpha 1‐adrenoceptor activation of a non‐selective cation current in rabbit portal vein by 1,2‐diacyl‐sn‐glycerol. , 1997, The Journal of physiology.

[54]  C. Romanin,et al.  Ca2+ Signaling by TRPC3 Involves Na+ Entry and Local Coupling to the Na+/Ca2+ Exchanger* , 2004, Journal of Biological Chemistry.