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Extracellular calcium is required for the maintenance of plasma membrane integrity in nucleated cells
In contrast to rat and human erythrocytes, nucleated erythrocytes from two fish species ( Cyprinus carpio and Salmo trutta) underwent almost complete haemolysis in 20 min of EDTA addition. Using Ca 2+/Mg 2+ EGTA-citrate buffer, we observed that half-maximal haemolysis of fish erythrocytes occurs at...
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Published in: | Cell calcium (Edinburgh) 2005-07, Vol.38 (1), p.53-57 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | In contrast to rat and human erythrocytes, nucleated erythrocytes from two fish species (
Cyprinus carpio and
Salmo trutta) underwent almost complete haemolysis in 20
min of EDTA addition. Using Ca
2+/Mg
2+ EGTA-citrate buffer, we observed that half-maximal haemolysis of fish erythrocytes occurs at [Ca
2+]
o ∼10
μM independently of extracellular Mg
2+ concentration. Attenuation of [Ca
2+]
o with EGTA also decreased stability of the plasma membrane of vascular smooth muscle cells (VSMC) and HeLa cells, indicated by a three- to five-fold elevation of lactate dehydrogenase release and passive permeability of plasma membrane for Na
+. In VSMC, EGTA lowered [Ca
2+]
i by ∼20%. This effect was absent in VSMC-loaded with the intracellular Ca
2+ chelator BAPTA. In contrast to EGTA, BAPTA did not affect haemoglobin release from fish erythrocytes and passive permeability for Na
+ in VSMC. Viewed collectively, our data show that in nucleated cells, extracellular Ca
2+ plays a crucial role in the maintenance of plasma membrane integrity. |
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ISSN: | 0143-4160 1532-1991 |
DOI: | 10.1016/j.ceca.2005.03.006 |