1. Src kinase controls signaling pathways in sensory neuron triggered by low-power infrared radiation
- Author
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S. A. Podzorova, I. V. Rogachevskii, V. A. Penniyaynen, Igor L. Yachnev, Boris V. Krylov, and V. B. Plakhova
- Subjects
0301 basic medicine ,Sensory Receptor Cells ,Neurite ,Infrared Rays ,Physiology ,G protein ,Sensory system ,Gating ,03 medical and health sciences ,Tissue culture ,0302 clinical medicine ,Physiology (medical) ,medicine ,Animals ,Rats, Wistar ,Pharmacology ,Chemistry ,Dose-Response Relationship, Radiation ,General Medicine ,Sensory neuron ,Rats ,Cell biology ,src-Family Kinases ,030104 developmental biology ,medicine.anatomical_structure ,Sodium-Potassium-Exchanging ATPase ,Signal transduction ,030217 neurology & neurosurgery ,Signal Transduction ,Proto-oncogene tyrosine-protein kinase Src - Abstract
Low-power (non-thermal) infrared (IR) radiation with the wavelength of 10.6 μm activates the Na,K-ATPase transducer function in sensory neurons, which is manifested in decrease of NaV1.8 channel voltage sensitivity at the cellular membrane level and in inhibition of growth of chick embryo dorsal root ganglia neurites at the tissue level. It is shown that the effect of low-power IR radiation is totally blocked by a specific Src kinase inhibitor, PP2. Upon irradiation on the background of PP2, the effective charge of NaV1.8 channel activation gating system does not differ from its control value in patch-clamp experiments, and the area index of sensory ganglia neurites growth remains unchanged as compared with the control in organotypic tissue culture. The data obtained demonstrate that Src kinase is involved in intracellular signaling pathways triggered by CO2 laser low-power IR radiation by the transducer-activated mechanism. This is the first indication that in primary sensory neuron the signals of low-power IR radiation are sensed, amplified, and transduced by the Na,K-ATPase/Src complex and not by G proteins.
- Published
- 2019
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