Protein Tyrosine Kinase Involvement in Learning-Produced Changes in Hermissenda Type B Photoreceptors
Autor: | Iksung Jin, Haojiang Huang, Benjamin E. Smith, Joseph Farley |
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Rok vydání: | 2009 |
Předmět: |
Physiology
Protein tyrosine phosphatase In Vitro Techniques Biophysical Phenomena Functional Laterality Membrane Potentials Phenols Conditioning Psychological medicine Animals Protein Kinase Inhibitors Protein Kinase C B cell Protein kinase C Membrane potential Kinase Chemistry Hermissenda General Neuroscience Depolarization Articles Protein-Tyrosine Kinases Genistein Electric Stimulation Cell biology Associative learning medicine.anatomical_structure Potassium Photoreceptor Cells Invertebrate Peptides Tyrosine kinase |
Zdroj: | Journal of Neurophysiology. 102:3573-3595 |
ISSN: | 1522-1598 0022-3077 |
DOI: | 10.1152/jn.90732.2008 |
Popis: | Learning-correlated changes in the excitability and photoresponses of Hermissenda 's ocular type B photoreceptors are mediated by reductions in two distinct K+currents, IAand IK-Ca. The suppression of these K+currents has been linked to conditioning-produced activation of protein kinase C (PKC). The question of whether PKC accounts completely for the changes in excitability and K+currents or whether other kinase(s) are involved has received little attention. In the present experiments, we asked whether protein tyrosine kinases (PTKs) might also contribute to conditioning-produced alterations in B cells. We found that the PTK inhibitors genistein and lavendustin A greatly reduced cumulative depolarization of type B cells, a short-term correlate of associative learning. This disruption occurred even when PKC activation had been either occluded by preexposure of type B cells to a phorbol ester or otherwise prevented by the pseudosubstrate inhibitor peptide PKC[19–31]. PTK inhibitors also increased the amplitude of the transient ( IA) and delayed ( IDelayed) components of voltage-dependent K+current that have previously been shown to be selectively reduced by conditioning and to contribute to cumulative depolarization. Genistein partially prevented the reduction of IAand IDelayeddue to in vitro conditioning and blocked the changes in their voltage dependencies. Ionophoresis of pervanadate ion, a potent inhibitor of protein tyrosine phosphatases, depolarized type B photoreceptors and occluded conditioning-produced cumulative depolarization. Pervanadate also suppressed IAand IDelayed, reduced their voltage dependence, and altered inactivation kinetics for IA, mimicking conditioning. Western blot analysis using a phosphotyrosine antibody indicated that conditioning increased the phosphotyrosine content of many proteins within the Hermissenda CNS. Collectively, our results suggest that in addition to PKC, one or more PTKs play an important role in conditioning-produced changes in type B cell excitability. PTKs and PKCs converge to effect reductions in B cell K+currents during conditioning, apparently through distinct biophysical mechanisms. |
Databáze: | OpenAIRE |
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