Protein kinase C-dependent phosphorylation of a ciliary membrane protein and inhibition of ciliary beating
Open Access
- 1 December 1993
- journal article
- Published by The Company of Biologists in Journal of Cell Science
- Vol. 106 (4) , 1211-1220
- https://doi.org/10.1242/jcs.106.4.1211
Abstract
The present study examined whether protein kinase C phosphorylated a ciliary protein and whether this phos-phorylation event was temporally correlated with a decrease in ciliary beat frequency. Activation of protein kinase C decreased ciliary beat frequency of sheep tracheal epithelium, an effect fully blockable by pretreat-ment of the tissue pieces with H-7, a protein kinase inhibitor. Using cilia removed from these epithelial sur-faces and incubated in solutions containing stimulators of protein kinase C along with [-32P]ATP or [-35S]ATP, a single protein target of ciliary protein kinase C activity was identified. The protein is a polypeptide of molecular mass 37 kDa (p37) as estimated by SDS-polyacrylamide gel electrophoresis. Protein kinase C dependency of p37 phosphorylation was proven by showing that Calphostin C, a specific protein kinase C inhibitor, blocked label incorporation into p37 com-pletely, and by demonstrating that purified protein kinase C phosphorylated p37. Inhibitors of cAMP-dependent kinase and calcium/calmodulin-dependent kinase did not change the phosphorylation of p37 in the presence of protein kinase C activators. p37 was recovered in a Triton X-100-extractable fraction of this cil-iary preparation, suggesting that p37 is membrane associated. This hypothesis was further supported by the fact that p37 was present in a pellet representing reconstituted membranes. Thin-layer electrophoresis revealed that p37 was phosphorylated on serine and tyrosine residues, suggesting that the activation of protein kinase C also stimulated tyrosine kinase activity. p37 did not precipitate with annexin I or II antibodies. These results show that sheep tracheal cilia contain protein kinase C activity and that activated protein kinase C phosphory-lates a membrane-associated ovine ciliary target, an effect temporally related to a protein kinase C-mediated decrease in ciliary beat frequency.Keywords
This publication has 31 references indexed in Scilit:
- Activation of protein kinase C and elevation of cAMP interact synergistically to raise c-Fos and AP-1 activity in Jurkat cellsEuropean Journal of Pharmacology: Molecular Pharmacology, 1992
- Identification of surface components of mammalian respiratory tract ciliaCell Motility, 1990
- In vitro phosphorylation of Paramecium axonemes and permeabilized cellsCell Motility, 1989
- Protein kinase C mediates platelet-derived growth factor-induced tyrosine phosphorylation of p42.The Journal of cell biology, 1988
- Stimulation of polyphosphoinositide turnover upon activation of protein kinases in human erythrocytesBiochimica et Biophysica Acta (BBA) - Molecular Cell Research, 1988
- Regulation of sperm flagellar motility by calcium and cAMP‐dependent phosphorylationJournal of Cellular Biochemistry, 1987
- K-252 compounds, novel and potent inhibitors of protein kinase C and cyclic nucleotide-dependent protein kinasesBiochemical and Biophysical Research Communications, 1986
- Isoquinolinesulfonamides, novel and potent inhibitors of cyclic nucleotide-dependent protein kinase and protein kinase CBiochemistry, 1984
- Microtubule-membrane interactions in cilia. II. Photochemical cross-linking of bridge structures and the identification of a membrane-associated dynein-like ATPase.The Journal of cell biology, 1980
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970