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.
Skip Nav Destination
Article navigation
1 April 1986
Article|
April 01 1986
Is a rise in intracellular concentration of free calcium necessary or sufficient for stimulated cytoskeletal-associated actin?
R I Sha'afi
J Shefcyk
R Yassin
T F Molski
M Volpi
P H Naccache
J R White
M B Feinstein
E L Becker
Online ISSN: 1540-8140
Print ISSN: 0021-9525
J Cell Biol (1986) 102 (4): 1459–1463.
Citation
R I Sha'afi, J Shefcyk, R Yassin, T F Molski, M Volpi, P H Naccache, J R White, M B Feinstein, E L Becker; Is a rise in intracellular concentration of free calcium necessary or sufficient for stimulated cytoskeletal-associated actin?. J Cell Biol 1 April 1986; 102 (4): 1459–1463. doi: https://doi.org/10.1083/jcb.102.4.1459
Download citation file:
Sign in
Don't already have an account? Register
Client Account
You could not be signed in. Please check your email address / username and password and try again.
Could not validate captcha. Please try again.
Sign in via your Institution
Sign in via your InstitutionSuggested Content
Email alerts
Advertisement
Advertisement