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- W3036596229 endingPage "14" @default.
- W3036596229 startingPage "5" @default.
- W3036596229 abstract "Abstract Neurotrophin signaling via receptor tyrosine kinases is essential for the development and function of the nervous system in vertebrates. TrkB activation and signaling show substantial differences to other receptor tyrosine kinases of the Trk family that mediate the responses to nerve growth factor and neurotrophin-3. Growing evidence suggests that TrkB cell surface expression is highly regulated and determines the sensitivity of neurons to brain-derived neurotrophic factor (BDNF). This translocation of TrkB depends on co-factors and modulators of cAMP levels, N-glycosylation, and receptor transactivation. This process can occur in very short time periods and the resulting rapid modulation of target cell sensitivity to BDNF could represent a mechanism for fine-tuning of synaptic plasticity and communication in complex neuronal networks. This review focuses on those modulatory mechanisms in neurons that regulate responsiveness to BDNF via control of TrkB surface expression." @default.
- W3036596229 created "2020-06-25" @default.
- W3036596229 creator A5022587380 @default.
- W3036596229 creator A5053245663 @default.
- W3036596229 creator A5084567774 @default.
- W3036596229 date "2020-06-15" @default.
- W3036596229 modified "2023-10-14" @default.
- W3036596229 title "Regulation of TrkB cell surface expression—a mechanism for modulation of neuronal responsiveness to brain-derived neurotrophic factor" @default.
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