Ca2+ transport and permeability in inside-out red cell membrane vesicles after freezing

Cryobiology ◽  
1986 ◽  
Vol 23 (2) ◽  
pp. 134-140 ◽  
Author(s):  
A. Rubinacci ◽  
B. Fuller ◽  
F. Wuytack ◽  
W. De Loecker
Science ◽  
1970 ◽  
Vol 168 (3928) ◽  
pp. 255-257 ◽  
Author(s):  
T. L. Steck ◽  
R. S. Weinstein ◽  
J. H. Straus ◽  
D. F. H. Wallach

1992 ◽  
Vol 48 (3) ◽  
pp. 235-240 ◽  
Author(s):  
Alessandro Rubinacci ◽  
Paola Divieti ◽  
Stefano Lodigiani ◽  
Alessandro De Ponti ◽  
Michele Samaja

1972 ◽  
Vol 59 (4) ◽  
pp. 462-475 ◽  
Author(s):  
Myra L. Weiner ◽  
Kwang Soo Lee

The relationship between active extrusion of Ca++ from red cell ghosts and active uptake of Ca++ by isolated red cell membrane fragments was investigated by studying the Ca++ uptake activities of inside-out and right side-out vesicles. Preparations A and B which had mainly inside-out and right side-out vesicles, respectively, were isolated from red cell membranes and were compared with respect to Ca++ adenosine triphosphatase (ATPase) and ATP-dependent Ca++ uptake activities. Preparation A had nearly eight times more inside-out vesicles and took up eight times more 45Ca in the presence of ATP compared to preparation B. Separation of the 45Ca-labeled membrane vesicles by density gradient centrifugation showed that the 45Ca label was localized to the inside-out vesicle fraction. In addition, the 45Ca taken up in the presence of ATP was lost during a subsequent incubation in the absence of ATP. The rate of 45Ca loss was not influenced by the presence of EGTA, but was slowed in the presence of La+8 (0.1 mM) in the efflux medium. The results presented here support the thesis that the active uptake of Ca++ by red cell membrane fragments is due to the active transport of Ca++ into inside-out vesicles.


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