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cAMP and cGMP Play an Essential Role in Galvanotaxis of Cell Fragments.
- Source :
-
Journal of cellular physiology [J Cell Physiol] 2016 Jun; Vol. 231 (6), pp. 1291-300. Date of Electronic Publication: 2015 Nov 24. - Publication Year :
- 2016
-
Abstract
- Cell fragments devoid of the nucleus and major organelles are found in physiology and pathology, for example platelets derived from megakaryocytes, and cell fragments from white blood cells and glioma cells. Platelets exhibit active chemotaxis. Fragments from white blood cells display chemotaxis, phagocytosis, and bactericidal functions. Signaling mechanisms underlying migration of cell fragments are poorly understood. Here we used fish keratocyte fragments and demonstrated striking differences in signal transduction in migration of cell fragments and parental cells in a weak electric field. cAMP or cGMP agonists completely abolished directional migration of fragments, but had no effect on parental cells. The inhibition effects were prevented by pre-incubating with cAMP and cGMP antagonists. Blocking cAMP and cGMP downstream signaling by inhibition of PKA and PKG also recovered fragment galvanotaxis. Both perturbations confirmed that the inhibitory effect was mediated by cAMP or cGMP signaling. Inhibition of cathode signaling with PI3K inhibitor LY294002 also prevented the effects of cAMP or cGMP agonists. Our results suggest that cAMP and cGMP are essential for galvanotaxis of cell fragments, in contrast to the signaling mechanisms in parental cells.<br /> (© 2015 Wiley Periodicals, Inc.)
- Subjects :
- Animals
Cell-Derived Microparticles drug effects
Cells, Cultured
Cyclic AMP-Dependent Protein Kinases antagonists & inhibitors
Cyclic AMP-Dependent Protein Kinases metabolism
Cyclic GMP-Dependent Protein Kinases antagonists & inhibitors
Cyclic GMP-Dependent Protein Kinases metabolism
Dose-Response Relationship, Drug
Electric Stimulation
Fibroblasts drug effects
Fishes
Phosphatidylinositol 3-Kinase metabolism
Phosphoinositide-3 Kinase Inhibitors
Protein Kinase Inhibitors pharmacology
Time Factors
Cell Movement drug effects
Cell-Derived Microparticles metabolism
Cyclic AMP metabolism
Cyclic GMP metabolism
Fibroblasts metabolism
Second Messenger Systems drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1097-4652
- Volume :
- 231
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Journal of cellular physiology
- Publication Type :
- Academic Journal
- Accession number :
- 26517849
- Full Text :
- https://doi.org/10.1002/jcp.25229