The role of calcium ions for the expression of ricin toxicity in cultured macrophages

✍ Scribed by Naseem, Syed M. ;Wellner, Robert B. ;Pace, Judith G.

• Publisher: John Wiley and Sons
• Year: 1992
• Tongue: English
• Weight: 574 KB
• Volume: 7
• Category: Article
• ISSN: 0887-2082
• DOI: 10.1002/jbt.2570070211

✦ Synopsis

Rich toxin, which consists of two distinct polypeptide moieties, A and B chains, is cytotoxic to the cultured macrophage cell line, J774A.1. Ricin is a protein synthesis inhibitor, and incubating macrophages for 4 hours with ricin (1 pM to 10 nM) in standard medium containing calcium and magnesium inhibited 3H-leucine incorporation into protein (97%, at 1 nM ricin). However, in Ca2+-free medium, protein synthesis was inhibited only 19%. EGTA pretreatment (to deplete intracellular calcium) also partly protected cells from protein synthesis inhibition, in spite of added calcium (2 mM) in the incubation medium. Decreased toxicity in the absence of extracellular calcium resulted from decreased toxin binding. Adding or deleting Mg2+ did not affect protein synthesis or binding of lZ5I-ricin in cultured macrophages. We conclude that calcium is required for ricin to exert its inhibitory effect on protein synthesis in cultured macrop hages.