Show simple item record

dc.contributor.authorZhang, Luo
dc.contributor.authorSanderson, Michael J.
dc.date2022-08-11T08:09:34.000
dc.date.accessioned2022-08-23T16:35:42Z
dc.date.available2022-08-23T16:35:42Z
dc.date.issued2003-06-24
dc.date.submitted2009-03-26
dc.identifier.citation<p>J Physiol. 2003 Sep 15;551(Pt 3):765-76. Epub 2003 Jun 20. <a href="http://dx.doi.org/10.1113/jphysiol.2003.041707">Link to article on publisher's site</a></p>
dc.identifier.issn0022-3751 (Print)
dc.identifier.doi10.1113/jphysiol.2003.041707
dc.identifier.pmid12819300
dc.identifier.urihttp://hdl.handle.net/20.500.14038/38621
dc.description.abstractThe involvement of cyclic guanosine 3',5'-monophosphate (cGMP) and cGMP-dependent protein kinase (PKG) and their interaction with the Ca2+-dependent mechanisms in the regulation of ciliary activity are not well understood. To investigate how cGMP regulates ciliary activity, changes in ciliary beat frequency (CBF) and intracellular calcium concentration ([Ca2+]i) of rabbit tracheal ciliated cells in response to 8-bromo-cGMP (Br-cGMP) were simultaneously quantified using digital, high-speed phase-contrast and fluorescence imaging. Br-cGMP induced a response in ciliary activity that could be separated into two parts. Firstly, Br-cGMP induced a concentration-dependent increase in the basal CBF that occurred without increasing the [Ca2+]i. This response was not affected by excessively buffering the [Ca2+]i with BAPTA but was abolished by KT5823, a PKG inhibitor. Secondly, Br-cGMP induced a series of transient increases in CBF that were superimposed on the sustained increases in CBF. These transient increases in CBF correlated with the stimulation of a series of transient increases in [Ca2+]i and were abolished by BAPTA, but were unaffected by KT5823. The magnitude of the transient increases in CBF and [Ca2+]i were not dependent on the concentration of Br-cGMP. The Ca2+-dependent changes in CBF induced by ionomycin or ATP were not affected by KT5823. From these results, we propose that cGMP increases CBF in two ways: firstly through a Ca2+-independent mechanism involving PKG, and secondly through a Ca2+-dependent mechanism following the stimulation of changes in [Ca2+]i. In addition, we suggest that the Ca2+-dependent stimulation of rabbit airway ciliary activity does not initially require PKG activation.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=12819300&dopt=Abstract">Link to Article in PubMed</a></p>
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2343278/
dc.subjectAnimals
dc.subjectBuffers
dc.subjectCalcium
dc.subjectCalcium Signaling
dc.subjectCarbazoles
dc.subjectCells, Cultured
dc.subjectCilia
dc.subjectCyclic GMP
dc.subjectCyclic GMP-Dependent Protein Kinases
dc.subjectDose-Response Relationship, Drug
dc.subjectEnzyme Inhibitors
dc.subjectIndoles
dc.subjectIonomycin
dc.subjectIonophores
dc.subjectRabbits
dc.subjectRespiratory Mucosa
dc.subjectTrachea
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleThe role of cGMP in the regulation of rabbit airway ciliary beat frequency
dc.typeJournal Article
dc.source.journaltitleThe Journal of physiology
dc.source.volume551
dc.source.issuePt 3
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/1483
dc.identifier.contextkey798458
html.description.abstract<p>The involvement of cyclic guanosine 3',5'-monophosphate (cGMP) and cGMP-dependent protein kinase (PKG) and their interaction with the Ca2+-dependent mechanisms in the regulation of ciliary activity are not well understood. To investigate how cGMP regulates ciliary activity, changes in ciliary beat frequency (CBF) and intracellular calcium concentration ([Ca2+]i) of rabbit tracheal ciliated cells in response to 8-bromo-cGMP (Br-cGMP) were simultaneously quantified using digital, high-speed phase-contrast and fluorescence imaging. Br-cGMP induced a response in ciliary activity that could be separated into two parts. Firstly, Br-cGMP induced a concentration-dependent increase in the basal CBF that occurred without increasing the [Ca2+]i. This response was not affected by excessively buffering the [Ca2+]i with BAPTA but was abolished by KT5823, a PKG inhibitor. Secondly, Br-cGMP induced a series of transient increases in CBF that were superimposed on the sustained increases in CBF. These transient increases in CBF correlated with the stimulation of a series of transient increases in [Ca2+]i and were abolished by BAPTA, but were unaffected by KT5823. The magnitude of the transient increases in CBF and [Ca2+]i were not dependent on the concentration of Br-cGMP. The Ca2+-dependent changes in CBF induced by ionomycin or ATP were not affected by KT5823. From these results, we propose that cGMP increases CBF in two ways: firstly through a Ca2+-independent mechanism involving PKG, and secondly through a Ca2+-dependent mechanism following the stimulation of changes in [Ca2+]i. In addition, we suggest that the Ca2+-dependent stimulation of rabbit airway ciliary activity does not initially require PKG activation.</p>
dc.identifier.submissionpathoapubs/1483
dc.contributor.departmentDepartment of Physiology
dc.source.pages765-76


This item appears in the following Collection(s)

Show simple item record