Abstract
The addition of the calcium ionophore A23187 to rabbit neutrophils increases the amount of actin associated with the cytoskeleton regardless of the presence or absence of calcium in the incubation medium. In the presence of extracellular calcium, the effect of A23187 is biphasic with respect to concentration. The action of the ionophore is rapid, transient, and is inhibited by pertussis toxin, hyperosmolarity, and quinacrine. On the other hand, the addition of pertussis toxin or hyperosmolarity has small if any, effect on the rise in intracellular calcium produced by A23187. While quinacrine does not affect the fMet-Leu-Phe-induced increase in cytoskeletal actin and the polyphosphoinositide turnover, its addition inhibits completely the stimulated increase in Ca-influx produced by the same stimulus. The results presented here suggest that a rise in the intracellular concentration of free calcium is neither necessary nor sufficient for the stimulated increase in cytoskeletal-associated actin. A possible relationship between the lipid remodeling stimulated by chemoattractants and the increased cytoskeletal actin is discussed.
MeSH Terms
Actins/metabolism
Aminoquinolines
Animals
Arachidonic Acid
Arachidonic Acids/pharmacology
Calcimycin/pharmacology
Calcium/metabolism
Cytoskeletal Proteins/isolation & purification,metabolism
Cytoskeleton/drug effects,metabolism
Fluorescent Dyes
Kinetics
N-Formylmethionine Leucyl-Phenylalanine/pharmacology
Neutrophils/metabolism
Rabbits
Tetradecanoylphorbol Acetate/pharmacology
Chemicals
Actins
Aminoquinolines
Arachidonic Acids
Cytoskeletal Proteins
Fluorescent Dyes
Arachidonic Acid
Calcimycin
N-Formylmethionine Leucyl-Phenylalanine
Tetradecanoylphorbol Acetate
Quin2
Calcium
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Sha'afi R I
Shefcyk J
Yassin R
Molski T F
Volpi M
Naccache P H
White J R
Feinstein M B
Becker E L
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