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Diacylglycerols and PMA are particularly effective stimulators of fluid pinocytosis in human neutrophils.
- Source :
-
Journal of cellular physiology [J Cell Physiol] 1990 Dec; Vol. 145 (3), pp. 465-71. - Publication Year :
- 1990
-
Abstract
- Diacylglycerols (OAG, diC8) and PMA were found to stimulate fluid pinocytosis (net uptake of FITC-dextran) to a far greater extent than other neutrophil activators, such as the chemotactic agents fNLPNTL and LTB4, the microtubule disassembling agents colchicine and nocodazole, the kinase inhibitor H-7, or D2O. OAG and diC8 produce a dose-dependent increase in the uptake of FITC-dextran, which is up to about 25- to 30-fold the control value of unstimulated neutrophils. The protein kinase inhibitor H-7 alone had a small stimulating effect on the net uptake, and it failed to inhibit stimulation of fluid pinocytosis by PMA, OAG, and diC8. Also, the protein kinase inhibitor staurosporine failed to inhibit fluid pinocytosis stimulated by OAG, diC8, and PMA. Stimulated fluid pinocytosis and vacuolization in response to PMA or diacylglycerols is associated with surface ruffling of neutrophils. Pinocytosis as well as surface ruffling stimulated by PMA, OAG, diC8, or diC10 are suppressed in the presence of cytochalasin D. The results suggest that diacylglycerols may be instrumental in transducing the signal for stimulated pinocytosis and that the surface movements induced by diacylglycerols, and PMA may be instrumental in fluid pinocytosis.
- Subjects :
- 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine
Alkaloids pharmacology
Chemotaxis, Leukocyte drug effects
Colchicine pharmacology
Humans
In Vitro Techniques
Isoquinolines pharmacology
Kinetics
Leukotriene B4 pharmacology
Neutrophils cytology
Neutrophils drug effects
Nocodazole pharmacology
Oligopeptides pharmacology
Piperazines pharmacology
Protein Kinase Inhibitors
Staurosporine
Diglycerides pharmacology
Neutrophils physiology
Pinocytosis drug effects
Tetradecanoylphorbol Acetate pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 0021-9541
- Volume :
- 145
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Journal of cellular physiology
- Publication Type :
- Academic Journal
- Accession number :
- 2177059
- Full Text :
- https://doi.org/10.1002/jcp.1041450311