Volumetric Deformation of Live Cells Induced by Pressure-Activated Cross-Membrane Ion Transport

2014 ◽  
Vol 113 (11) ◽  
Author(s):  
T. H. Hui ◽  
Z. L. Zhou ◽  
J. Qian ◽  
Y. Lin ◽  
A. H. W. Ngan ◽  
...  
2002 ◽  
Vol 43 (29) ◽  
pp. 5145-5147 ◽  
Author(s):  
Darshan Ranganathan ◽  
Manoj P Samant ◽  
R Nagaraj ◽  
E Bikshapathy

2013 ◽  
Vol 304 (1) ◽  
pp. H94-H103 ◽  
Author(s):  
Aude Belliard ◽  
Yoann Sottejeau ◽  
Qiming Duan ◽  
Jessa L. Karabin ◽  
Sandrine V. Pierre

Na+,K+-ATPase and cell survival were investigated in a cellular model of ischemia-reperfusion (I/R)-induced injury and protection by ouabain-induced preconditioning (OPC). Rat neonatal cardiac myocytes were subjected to 30 min of substrate and coverslip-induced ischemia followed by 30 min of simulated reperfusion. This significantly compromised cell viability as documented by lactate dehydrogenase release and Annexin V/propidium iodide staining. Total Na+,K+-ATPase α1- and α3-polypeptide expression remained unchanged, but cell surface biotinylation and immunostaining studies revealed that α1-cell surface abundance was significantly decreased. Na+,K+-ATPase-activity in crude homogenates and 86Rb+ transport in live cells were both significantly decreased by about 30% after I/R. OPC, induced by a 4-min exposure to 10 μM ouabain that ended 8 min before the beginning of ischemia, increased cell viability in a PKCε-dependent manner. This was comparable with the protective effect of OPC previously reported in intact heart preparations. OPC prevented I/R-induced decrease of Na+,K+-ATPase activity and surface expression. This model also revealed that Na+,K+-ATPase-mediated 86Rb+ uptake was not restored to control levels in the OPC group, suggesting that the increased viability was not conferred by an increased Na+,K+-ATPase-mediated ion transport capacity at the cell membrane. Consistent with this observation, transient expression of an internalization-resistant mutant form of Na+,K+-ATPase α1 known to have increased surface abundance without increased ion transport activity successfully reduced I/R-induced cell death. These results suggest that maintenance of Na+,K+-ATPase cell surface abundance is critical to myocyte survival after an ischemic attack and plays a role in OPC-induced protection. They further suggest that the protection conferred by increased surface expression of Na+,K+-ATPase may be independent of ion transport.


2000 ◽  
Vol 65 (2) ◽  
pp. 365-374 ◽  
Author(s):  
Darshan Ranganathan ◽  
V. Haridas ◽  
Sunita Kurur ◽  
R. Nagaraj ◽  
E. Bikshapathy ◽  
...  

1991 ◽  
Vol 47 (6) ◽  
pp. 850-857 ◽  
Author(s):  
Said Hajem ◽  
Patrick Hannaert ◽  
Thierry Moreau ◽  
Joseph Lellouch ◽  
Guy Huel ◽  
...  

1995 ◽  
Vol 29 (3) ◽  
pp. 171-174 ◽  
Author(s):  
L. L. Stotskaya ◽  
A. V. Serbin ◽  
K. Munshi ◽  
K. N. Kozeletskaya ◽  
A. A. Sominina ◽  
...  

1985 ◽  
Vol 30 (4) ◽  
pp. 712
Author(s):  
Ricardo Garay ◽  
Bernadette Dunham ◽  
Cielia Rosati ◽  
Corinne Nazaret ◽  
Pierre Braquet

2003 ◽  
Vol 26 (5) ◽  
pp. 397-404 ◽  
Author(s):  
Martina VOKURKOVÁ ◽  
Zdena DOBEŠOVÁ ◽  
Jaroslav KUNEŠ ◽  
Josef ZICHA

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