scholarly journals Recycling endosomes in neuronal membrane traffic

2007 ◽  
Vol 99 (6) ◽  
pp. 333-342 ◽  
Author(s):  
Michael R. Schmidt ◽  
Volker Haucke
2018 ◽  
Author(s):  
Eva P. Karasmanis ◽  
Cat-Thi Phan ◽  
Dimitrios Angelis ◽  
Ilona A. Kesisova ◽  
Casper C. Hoogenraad ◽  
...  

2018 ◽  
Vol 46 (4) ◽  
pp. 518-524 ◽  
Author(s):  
Eva P. Karasmanis ◽  
Cat-Thi Phan ◽  
Dimitrios Angelis ◽  
Ilona A. Kesisova ◽  
Casper C. Hoogenraad ◽  
...  

Neuron ◽  
2003 ◽  
Vol 37 (3) ◽  
pp. 433-447 ◽  
Author(s):  
Mala Murthy ◽  
Dan Garza ◽  
Richard H. Scheller ◽  
Thomas L. Schwarz

2005 ◽  
Vol 16 (2) ◽  
pp. 849-860 ◽  
Author(s):  
Gayle M. Wilson ◽  
Andrew B. Fielding ◽  
Glenn C. Simon ◽  
Xinzi Yu ◽  
Paul D. Andrews ◽  
...  

An integral part of cell division is the separation of daughter cells via cytokinesis. There is now good evidence that the completion of cytokinesis requires coordinated membrane trafficking to deliver new membrane to the tip of the furrow and to complete the abscission. Here we have examined membrane traffic in cytokinesis and describe several novel observations. First, we show that Rab11- and FIP3-containing recycling endosomes accumulate near the cleavage furrow and are required for successful completion of cytokinesis. Second, we demonstrate that the Rab11-FIP3 protein complex is intimately involved in the delivery of endosomes to the cleavage furrow. Significantly, although FIP3 recruitment to endosomes is Rab11 dependent, we find that the targeting of FIP3 to the midbody is independent of Rab11. Third, we show that the Rab11-FIP3 complex is required for a late stage of cytokinesis, possibly abscission. Finally, we demonstrate that localization of FIP3 is subject to substantial spatial and temporal regulation. These data provide the first detailed analysis of recycling endosomes in cell division and provide a new model for membrane traffic to the furrow. We propose that the dynamic Rab11-FIP3 interaction controls the delivery, targeting, and fusion of recycling endosomes with furrow during late cytokinesis and abscission.


2000 ◽  
Vol 20 (23) ◽  
pp. 8551-8565 ◽  
Author(s):  
Xiaolu Wang ◽  
Friedrich W. Herberg ◽  
Michael M. Laue ◽  
Christiane Wüllner ◽  
Bin Hu ◽  
...  

2008 ◽  
Vol 19 (6) ◽  
pp. 2650-2660 ◽  
Author(s):  
Ray Ishizaki ◽  
Hye-Won Shin ◽  
Hiroko Mitsuhashi ◽  
Kazuhisa Nakayama

BIG2 and BIG1 are closely related guanine-nucleotide exchange factors (GEFs) for ADP-ribosylation factors (ARFs) and are involved in the regulation of membrane traffic through activating ARFs and recruiting coat protein complexes, such as the COPI complex and the AP-1 clathrin adaptor complex. Although both ARF-GEFs are associated mainly with the trans-Golgi network (TGN) and BIG2 is also associated with recycling endosomes, it is unclear whether BIG2 and BIG1 share some roles in membrane traffic. We here show that knockdown of both BIG2 and BIG1 by RNAi causes mislocalization of a subset of proteins associated with the TGN and recycling endosomes and blocks retrograde transport of furin from late endosomes to the TGN. Similar mislocalization and protein transport block, including furin, were observed in cells depleted of AP-1. Taken together with previous reports, these observations indicate that BIG2 and BIG1 play redundant roles in trafficking between the TGN and endosomes that involves the AP-1 complex.


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