Protein kinase C enhances the swelling-induced chloride current in human atrial myocytes

Author(s):  
Ye-tao Li ◽  
Xin-ling Du
2000 ◽  
Vol 278 (2) ◽  
pp. H670-H676 ◽  
Author(s):  
Christophe Boixel ◽  
Sophie Tessier ◽  
Yves Pansard ◽  
Loïc Lang-Lazdunski ◽  
Jean-Jacques Mercadier ◽  
...  

The effects of tyrosine protein kinases (TK) on the L-type Ca2+ current ( I Ca) were examined in whole cell patch-clamped human atrial myocytes. The TK inhibitors genistein (50 μM), lavendustin A (50 μM), and tyrphostin 23 (50 μM) stimulated I Ca by 132 ± 18% ( P < 0.001), 116 ± 18% ( P < 0.05), and 60 ± 6% ( P < 0.001), respectively. After I Castimulation by genistein, external application of isoproterenol (1 μM) caused an additional increase in I Ca. Dialyzing the cells with a protein kinase A inhibitor suppressed the effect of isoproterenol on I Ca but not that of genistein. Inhibition of protein kinase C (PKC) by pretreatment of cells with 100 nM staurosporine or 100 nM calphostin C prevented the effects of genistein on I Ca. The PKC activator phorbol 12-myristate 13-acetate (PMA), after an initial stimulation (75 ± 17%, P < 0.05), decreased I Ca(−36 ± 5%, P < 0.001). Once the inhibitory effect of PMA on I Ca had stabilized, genistein strongly stimulated the current (323 ± 25%, P < 0.05). Pretreating myocytes with genistein reduced the inhibitory effect of PMA on I Ca. We conclude that, in human atrial myocytes, TK inhibit I Ca via a mechanism that involves PKC.


2005 ◽  
Vol 35 (11) ◽  
pp. 812
Author(s):  
Dawon Kang ◽  
Hong Sik Lee ◽  
Seong Geun Hong ◽  
Jaehee Han

1991 ◽  
Vol 69 (10) ◽  
pp. 1514-1524 ◽  
Author(s):  
Heikki Ruskoaho ◽  
Päivi Kinnunen ◽  
Pentti Mäntymaa ◽  
Paavo Uusimaa ◽  
Tarja Taskinen ◽  
...  

Atrial natriuretic factor (ANF), a peptide hormone that regulates salt and water balance and blood pressure, is synthesized, stored, and secreted from mammalian myocytes. Stretching of atrial myocytes stimulates ANF secretion, but the cellular processes involved in linking mechanical distension to ANF release are unknown. We reported that phorbol esters, which mimic the action of diacylglycerol by acting directly on protein kinase C and the Ca2+ ionophore A23187, which introduces free Ca2+ into the cell, both increase basal ANF secretion in the isolated perfused rat heart. Phorbol ester also increased responsiveness to Ca2+ channel agonists, such as Bay k8644, and to agents that increase cAMP, such as forskolin and membrane-permeable cAMP analogs. In neonatal cultured rat atrial myocytes, protein kinase C activation by 12-O-tetradecanoylphorbol 13-acetate stimulated ANF secretion, whereas the release was unresponsive to changes in intracellular Ca2+. Endothelin, which stimulates phospholipase C mediated hydrolysis of phosphoinositides and activates protein kinase C, increased both basal and atrial stretch-induced ANF secretion from isolated perfused rat hearts. Similarly, phorbol ester enhanced atrial stretch-stimulated ANF secretion, while the increase in intracellular Ca2+ appeared to be negatively coupled to the stretch-induced ANF release. Finally, phorbol ester stimulated ANF release from the severely hypertrophied ventricles of hypertensive animals but not from normal rat myocardium. These results suggest that the protein kinase C activity may play an important role in the regulation of basal ANF secretion both from atria and ventricular cells, and that stretch of atrial myocytes appears to be positively modulated by phorbol esters.Key words: hormone secretion, atrial stretch, protein kinase C, phosphoinositide hydrolysis, cellular calcium.


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