AP180 Couples Protein Retrieval to Clathrin‐Mediated Endocytosis of Synaptic Vesicles. (26th February 2014)
- Record Type:
- Journal Article
- Title:
- AP180 Couples Protein Retrieval to Clathrin‐Mediated Endocytosis of Synaptic Vesicles. (26th February 2014)
- Main Title:
- AP180 Couples Protein Retrieval to Clathrin‐Mediated Endocytosis of Synaptic Vesicles
- Authors:
- Vanlandingham, Phillip A.
Barmchi, Mojgan Padash
Royer, Suzanne
Green, Rebekah
Bao, Hong
Reist, Noreen
Zhang, Bing - Abstract:
- <abstract abstract-type="main" id="tra12153-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <p id="tra12153-para-0001">How clathrin‐mediated endocytosis (CME) retrieves vesicle proteins into newly formed synaptic vesicles (SVs) remains a major puzzle. Besides its roles in stimulating clathrin‐coated vesicle formation and regulating SV size, the clathrin assembly protein AP180 has been identified as a key player in retrieving SV proteins. The mechanisms by which AP180 recruits SV proteins are not fully understood. Here, we show that following acute inactivation of AP180 in <italic>Drosophila</italic>, SV recycling is severely impaired at the larval neuromuscular synapse based on analyses of FM 1‐43 uptake and synaptic ultrastructure. More dramatically, AP180 activity is important to maintain the integrity of SV protein complexes at the plasma membrane during endocytosis. These observations suggest that AP180 normally clusters SV proteins together during recycling. Consistent with this notion, SV protein composition and distribution are altered in AP180 mutant flies. Finally, AP180 co‐immunoprecipitates with SV proteins, including the vesicular glutamate transporter and neuronal synaptobrevin. These results reveal a new mode by which AP180 couples protein retrieval to CME of SVs. AP180 is also genetically linked to Alzheimer's disease. Hence, the findings of this study may provide new mechanistic insight into the role of AP180 dysfunction in Alzheimer's<abstract abstract-type="main" id="tra12153-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <p id="tra12153-para-0001">How clathrin‐mediated endocytosis (CME) retrieves vesicle proteins into newly formed synaptic vesicles (SVs) remains a major puzzle. Besides its roles in stimulating clathrin‐coated vesicle formation and regulating SV size, the clathrin assembly protein AP180 has been identified as a key player in retrieving SV proteins. The mechanisms by which AP180 recruits SV proteins are not fully understood. Here, we show that following acute inactivation of AP180 in <italic>Drosophila</italic>, SV recycling is severely impaired at the larval neuromuscular synapse based on analyses of FM 1‐43 uptake and synaptic ultrastructure. More dramatically, AP180 activity is important to maintain the integrity of SV protein complexes at the plasma membrane during endocytosis. These observations suggest that AP180 normally clusters SV proteins together during recycling. Consistent with this notion, SV protein composition and distribution are altered in AP180 mutant flies. Finally, AP180 co‐immunoprecipitates with SV proteins, including the vesicular glutamate transporter and neuronal synaptobrevin. These results reveal a new mode by which AP180 couples protein retrieval to CME of SVs. AP180 is also genetically linked to Alzheimer's disease. Hence, the findings of this study may provide new mechanistic insight into the role of AP180 dysfunction in Alzheimer's disease.</p> <p> <inline-graphic xlink:href="ark:/27927/pgg4swwqj8b" mimetype="image" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink" /> </p> </abstract> … (more)
- Is Part Of:
- Traffic. Volume 15:Number 4(2014:Apr.)
- Journal:
- Traffic
- Issue:
- Volume 15:Number 4(2014:Apr.)
- Issue Display:
- Volume 15, Issue 4 (2014)
- Year:
- 2014
- Volume:
- 15
- Issue:
- 4
- Issue Sort Value:
- 2014-0015-0004-0000
- Page Start:
- 433
- Page End:
- 450
- Publication Date:
- 2014-02-26
- Subjects:
- Biological transport -- Periodicals
571.6 - Journal URLs:
- http://www.blackwell-synergy.com/Journals/member/institutions/issuelist.asp?journal=tra ↗
http://www.blackwellpublishing.com/journal.asp?ref=1398-9219&site=1 ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1600-0854 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/tra.12153 ↗
- Languages:
- English
- ISSNs:
- 1398-9219
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8881.575000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3717.xml