Synapsins regulate brain‐derived neurotrophic factor‐mediated synaptic potentiation and axon elongation by acting on membrane rafts. (21st March 2017)
- Record Type:
- Journal Article
- Title:
- Synapsins regulate brain‐derived neurotrophic factor‐mediated synaptic potentiation and axon elongation by acting on membrane rafts. (21st March 2017)
- Main Title:
- Synapsins regulate brain‐derived neurotrophic factor‐mediated synaptic potentiation and axon elongation by acting on membrane rafts
- Authors:
- Kao, Hung‐Teh
Ryoo, Kanghyun
Lin, Albert
Janoschka, Stephen R.
Augustine, George J.
Porton, Barbara - Editors:
- Kano, Masanobu
- Abstract:
- Abstract: In neurons, intracellular membrane rafts are essential for specific actions of brain‐derived neurotrophic factor (BDNF), which include the regulation of axon outgrowth, growth cone turning and synaptic transmission. Virtually, all the actions of BDNF are mediated by binding to its receptor, TrkB. The association of TrkB with the tyrosine kinase, Fyn, is critical for its localization to intracellular membrane rafts. Here, we show that synapsins, a family of highly amphipathic neuronal phosphoproteins, regulate membrane raft lipid composition and consequently, the ability of BDNF to regulate axon/neurite development and potentiate synaptic transmission. In the brains of mice lacking all synapsins, the expression of both BDNF and TrkB were increased, suggesting that BDNF/TrkB‐mediated signaling is impaired. Consistent with this finding, synapsin‐depleted neurons exhibit altered raft lipid composition, deficient targeting of Fyn to rafts, attenuated TrkB activation, and abrogation of BDNF‐stimulated axon outgrowth and synaptic potentiation. Conversely, overexpression of synapsins in neuroblastoma cells results in corresponding reciprocal changes in raft lipid composition, increased localization of Fyn to rafts and promotion of BDNF‐stimulated neurite formation. In the presence of synapsins, the ratio of cholesterol to estimated total phospholipids converged to 1, suggesting that synapsins act by regulating the ratio of lipids in intracellular membranes, therebyAbstract: In neurons, intracellular membrane rafts are essential for specific actions of brain‐derived neurotrophic factor (BDNF), which include the regulation of axon outgrowth, growth cone turning and synaptic transmission. Virtually, all the actions of BDNF are mediated by binding to its receptor, TrkB. The association of TrkB with the tyrosine kinase, Fyn, is critical for its localization to intracellular membrane rafts. Here, we show that synapsins, a family of highly amphipathic neuronal phosphoproteins, regulate membrane raft lipid composition and consequently, the ability of BDNF to regulate axon/neurite development and potentiate synaptic transmission. In the brains of mice lacking all synapsins, the expression of both BDNF and TrkB were increased, suggesting that BDNF/TrkB‐mediated signaling is impaired. Consistent with this finding, synapsin‐depleted neurons exhibit altered raft lipid composition, deficient targeting of Fyn to rafts, attenuated TrkB activation, and abrogation of BDNF‐stimulated axon outgrowth and synaptic potentiation. Conversely, overexpression of synapsins in neuroblastoma cells results in corresponding reciprocal changes in raft lipid composition, increased localization of Fyn to rafts and promotion of BDNF‐stimulated neurite formation. In the presence of synapsins, the ratio of cholesterol to estimated total phospholipids converged to 1, suggesting that synapsins act by regulating the ratio of lipids in intracellular membranes, thereby promoting lipid raft formation. These studies reveal a mechanistic link between BDNF and synapsins, impacting early development and synaptic transmission. Abstract : We investigated the role of synapsins in neuronal development. The results show that synapsins regulate intracellular membrane raft lipid composition by restricting the ratio of cholesterol to total phospholipids, thereby promoting the localization of Fyn/TrkB to rafts, and subsequent activation of TrkB by BDNF. Consistent with these results, synapsins are required for BDNF‐stimulated axon outgrowth and synaptic potentiation, thus revealing mechanistic links between BDNF and synapsins. … (more)
- Is Part Of:
- European journal of neuroscience. Volume 45:Number 8(2017)
- Journal:
- European journal of neuroscience
- Issue:
- Volume 45:Number 8(2017)
- Issue Display:
- Volume 45, Issue 8 (2017)
- Year:
- 2017
- Volume:
- 45
- Issue:
- 8
- Issue Sort Value:
- 2017-0045-0008-0000
- Page Start:
- 1085
- Page End:
- 1101
- Publication Date:
- 2017-03-21
- Subjects:
- lipid -- mouse -- neurodevelopment -- signal transduction
Nervous system -- Periodicals
612.8 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1460-9568 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/ejn.13552 ↗
- Languages:
- English
- ISSNs:
- 0953-816X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3829.731700
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 2859.xml