scholarly journals Arterial smooth muscle cell PKD2 (TRPP1) channels regulate systemic blood pressure

eLife ◽  
2018 ◽  
Vol 7 ◽  
Author(s):  
Simon Bulley ◽  
Carlos Fernández-Peña ◽  
Raquibul Hasan ◽  
M Dennis Leo ◽  
Padmapriya Muralidharan ◽  
...  

Systemic blood pressure is determined, in part, by arterial smooth muscle cells (myocytes). Several Transient Receptor Potential (TRP) channels are proposed to be expressed in arterial myocytes, but it is unclear if these proteins control physiological blood pressure and contribute to hypertension in vivo. We generated the first inducible, smooth muscle-specific knockout mice for a TRP channel, namely for PKD2 (TRPP1), to investigate arterial myocyte and blood pressure regulation by this protein. Using this model, we show that intravascular pressure and α1-adrenoceptors activate PKD2 channels in arterial myocytes of different systemic organs. PKD2 channel activation in arterial myocytes leads to an inward Na+ current, membrane depolarization and vasoconstriction. Inducible, smooth muscle cell-specific PKD2 knockout lowers both physiological blood pressure and hypertension and prevents pathological arterial remodeling during hypertension. Thus, arterial myocyte PKD2 controls systemic blood pressure and targeting this TRP channel reduces high blood pressure.

2018 ◽  
Author(s):  
Simon Bulley ◽  
Carlos Fernandez-Pena ◽  
Raquibul Hasan ◽  
M. Dennis Leo ◽  
Padmapriya Muralidharan ◽  
...  

AbstractSystemic blood pressure is determined, in part, by arterial smooth muscle cells (myocytes). Several Transient Receptor Potential (TRP) channels are proposed to be expressed in arterial myocytes, but it is unclear if these proteins control physiological blood pressure and contribute to hypertension in vivo. We generated the first inducible, smooth muscle-specific knockout for a TRP channel, namely for PKD2 (TRPP1), to investigate arterial myocyte and blood pressure regulation by this protein. Using this model, we show that intravascular pressure and α1-receptors activate PKD2 channels in arterial myocytes of different systemic organs. PKD2 channel activation in arterial myocytes leads to an inward Na+ current, membrane depolarization and vasoconstriction. Inducible, smooth muscle cell-specific PKD2 knockout lowers both physiological blood pressure and hypertension and prevents pathological arterial remodeling during hypertension. In summary, we show for the first time that arterial myocyte PKD2 channels control systemic blood pressure and targeting reduces high blood pressure.


2018 ◽  
Author(s):  
Simon Bulley ◽  
Carlos Fernández-Peña ◽  
Raquibul Hasan ◽  
M Dennis Leo ◽  
Padmapriya Muralidharan ◽  
...  

2018 ◽  
Vol 32 (S1) ◽  
Author(s):  
Carlos Fernandez‐Pena ◽  
Simon Bulley ◽  
Raquibul Hasan ◽  
M. Dennis Leo ◽  
Padmapriya Muralidharan ◽  
...  

2018 ◽  
Author(s):  
Simon Bulley ◽  
Carlos Fernández-Peña ◽  
Raquibul Hasan ◽  
M Dennis Leo ◽  
Padmapriya Muralidharan ◽  
...  

eLife ◽  
2020 ◽  
Vol 9 ◽  
Author(s):  
Simon Bulley ◽  
Carlos Fernández-Peña ◽  
Raquibul Hasan ◽  
M Dennis Leo ◽  
Padmapriya Muralidharan ◽  
...  

Physiology ◽  
2004 ◽  
Vol 19 (2) ◽  
pp. 44-50 ◽  
Author(s):  
Judd W. Landsberg ◽  
Jason X.-J. Yuan

Ca2+ is a major trigger for pulmonary vasoconstriction and a stimulus for pulmonary vascular smooth muscle cell proliferation. The transient receptor potential cation channels participate in regulating intracellular Ca2+ and thus vascular contractility and cell proliferation. Upregulation of genes encoding these channels is involved in the development of pulmonary hypertension.


1996 ◽  
Vol 16 (6) ◽  
pp. 815-820 ◽  
Author(s):  
Marie-Luce Bochaton-Piallat ◽  
Patricia Ropraz ◽  
Françoise Gabbiani ◽  
Giulio Gabbiani

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