In situ capture of mu-calpain activation in platelets
In situ detection of calpain activation in intact cells has not been possible to date. Here we present the first direct evidence, employing a novel approach, that mu-calpain is rapidly activated at cell membranes in platelets upon a rise in intracellular calcium concentration. Immunoelectron microsc...
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Veröffentlicht in: | The Journal of biological chemistry 1993-04, Vol.268 (10), p.7422-7426 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | In situ detection of calpain activation in intact cells has not been possible to date. Here we present the first direct evidence,
employing a novel approach, that mu-calpain is rapidly activated at cell membranes in platelets upon a rise in intracellular
calcium concentration. Immunoelectron microscopy using antibodies capable of distinguishing between the pre- and postautolysis
forms of mu-calpain revealed that treatment of platelets with calcium ionophore causes the preautolysis form of the protease
to translocate from cytosol to membranes, where it becomes activated by autolysis. This indicates that proteins associated
with membranes serve as primary substrates for calpain in cells. |
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ISSN: | 0021-9258 1083-351X |
DOI: | 10.1016/s0021-9258(18)53191-4 |