Α-Synuclein – Regulator of Exocytosis, Endocytosis, or Both?. Issue 7 (July 2017)
- Record Type:
- Journal Article
- Title:
- Α-Synuclein – Regulator of Exocytosis, Endocytosis, or Both?. Issue 7 (July 2017)
- Main Title:
- Α-Synuclein – Regulator of Exocytosis, Endocytosis, or Both?
- Authors:
- Lautenschläger, Janin
Kaminski, Clemens F.
Kaminski Schierle, Gabriele S. - Abstract:
- Abstract : α-Synuclein is known as a presynaptic protein that binds to small synaptic vesicles. Recent studies suggest that α-synuclein is not only attracted to these tiny and therewith highly curved membranes, but that in fact the sensing and regulation of membrane curvature is part of its physiological function. Moreover, recent studies have suggested that α-synuclein plays a role in the endocytosis of synaptic vesicles, and have provided support for a function of α-synuclein during exo- and endocytosis in which curvature sensing and membrane stabilization are crucial steps. This review aims to highlight recent research in the field and adds a new picture on the function of α-synuclein in maintaining synaptic homeostasis upon intense and repetitive neuronal activity. Trends: Membrane remodeling processes are crucial steps for the exo- and endocytosis of synaptic vesicles. From structure–function relationships, α-synuclein has been proposed to be a curvature sensing and regulating protein, thus proposing a role in mechanisms of exo- and endocytosis. A function in exocytosis has been suggested (i) via mediating SNARE-complex assembly, (ii) curvature stabilization, thus preventing premature fusion of vesicles, and (iii) in tethering of synaptic vesicles via lipid binding of α-synuclein with both its N- and a more C-terminal region. Latest studies indicate a function of α-synuclein in synaptic vesicle endocytosis. (i) A possible function in clathrin-mediated endocytosis hasAbstract : α-Synuclein is known as a presynaptic protein that binds to small synaptic vesicles. Recent studies suggest that α-synuclein is not only attracted to these tiny and therewith highly curved membranes, but that in fact the sensing and regulation of membrane curvature is part of its physiological function. Moreover, recent studies have suggested that α-synuclein plays a role in the endocytosis of synaptic vesicles, and have provided support for a function of α-synuclein during exo- and endocytosis in which curvature sensing and membrane stabilization are crucial steps. This review aims to highlight recent research in the field and adds a new picture on the function of α-synuclein in maintaining synaptic homeostasis upon intense and repetitive neuronal activity. Trends: Membrane remodeling processes are crucial steps for the exo- and endocytosis of synaptic vesicles. From structure–function relationships, α-synuclein has been proposed to be a curvature sensing and regulating protein, thus proposing a role in mechanisms of exo- and endocytosis. A function in exocytosis has been suggested (i) via mediating SNARE-complex assembly, (ii) curvature stabilization, thus preventing premature fusion of vesicles, and (iii) in tethering of synaptic vesicles via lipid binding of α-synuclein with both its N- and a more C-terminal region. Latest studies indicate a function of α-synuclein in synaptic vesicle endocytosis. (i) A possible function in clathrin-mediated endocytosis has been proposed, but a function also seems likely in (ii) fast endocytotic pathways such as kiss-and-run, or in (iii) the recently discovered ultrafast endocytosis process. … (more)
- Is Part Of:
- Trends in cell biology. Volume 27:Issue 7(2017)
- Journal:
- Trends in cell biology
- Issue:
- Volume 27:Issue 7(2017)
- Issue Display:
- Volume 27, Issue 7 (2017)
- Year:
- 2017
- Volume:
- 27
- Issue:
- 7
- Issue Sort Value:
- 2017-0027-0007-0000
- Page Start:
- 468
- Page End:
- 479
- Publication Date:
- 2017-07
- Subjects:
- Cytology -- Periodicals
Cytology -- Research -- Periodicals
571.6 - Journal URLs:
- http://www.sciencedirect.com/science/journal/09628924 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.tcb.2017.02.002 ↗
- Languages:
- English
- ISSNs:
- 0962-8924
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 9049.552000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 8562.xml