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HCN Channels Are Not Required for Mechanotransduction in Sensory Hair Cells of the Mouse Inner Ear 英文参考文献.docVIP

HCN Channels Are Not Required for Mechanotransduction in Sensory Hair Cells of the Mouse Inner Ear 英文参考文献.doc

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HCN Channels Are Not Required for Mechanotransduction in Sensory Hair Cells of the Mouse Inner Ear 英文参考文献

HCNChannelsAreNotRequiredfor MechanotransductioninSensoryHairCellsoftheMouse InnerEar GeoffreyC.Horwitz,AndreaLelli,Gwenae¨lleS.G.Ge′le′oc,JeffreyR.Holt* DepartmentofNeuroscienceandDepartmentofOtolaryngology,UniversityofVirginiaSchoolofMedicine,Charlottesville,Virginia,UnitedStatesofAmerica Abstract The molecular composition of the hair cell transduction channel has not been identified. Here we explore the novel hypothesis that hair cell transduction channels include HCN subunits. The HCN family of ion channels includes four members, HCN1-4. They were orginally identified as the molecular correlates of the hyperpolarization-activated, cyclic nucleotide gated ion channels that carry currents known as If, IQ or Ih. However, based on recent evidence it has been suggested that HCN subunits may also be components of the elusive hair cell transduction channel. To investigate this hypothesis we examined expression of mRNA that encodes HCN1-4 in sensory epithelia of the mouse inner ear, immunolocalization of HCN subunits 1, 2 and 4, uptake of the transduction channel permeable dye, FM1-43 and electrophysiologicalmeasurementofmechanotransductioncurrent.Dyeuptakeandtransductioncurrentwereassayedin cochlearandvestibularhaircellsofwildtypemiceexposedtoHCNchannelblockersoradominant-negativeformofHCN2 thatcontainedaporemutationandinmutantmicethatlackedHCN1,HCN2orboth.WefoundrobustexpressionofHCNs 1,2and4butlittleevidencethatlocalizedHCNsubunitsinhairbundles,thesiteofmechanotransduction.Althoughhigh concentrations of the HCN antagonist, ZD7288, blocked 50–70% of the transduction current, we found no reduction of transductioncurrentineithercochlearorvestibularhaircellsofHCN1-orHCN2-deficientmicerelativetowild-typemice. Furthermore, mice that lacked both HCN1 and HCN2 also had normal transduction currents. Lastly, we found that mice exposed tothe dominant-negative mutant form of HCN2 had normal transduction currents aswell. Taken together, the evidencesuggeststhatHCNsubunitsarenot

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