|
|
|
||||
| Home Help Feedback Subscriptions Archive Search Table of Contents | |||||
First published online 12 September 2006
doi: 10.1242/jcs.03167
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Research Article |
1 Institute for Molecular Bioscience and ARC Centre in Bioinformatics, University of Queensland, St. Lucia, QLD 4072, Australia
2 The Russell Grimwade School of Biochemistry and Molecular Biology and Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Melbourne, VIC 3010, Australia
* Author for correspondence (e-mail: R.Teasdale{at}imb.uq.edu.au)
Accepted 14 July 2006
We report that phosphoinositol-binding sorting nexin 5 (SNX5) associates with newly formed macropinosomes induced by EGF stimulation. We used the recruitment of GFP-SNX5 to macropinosomes to track their maturation. Initially, GFP-SNX5 is sequestered to discrete subdomains of the macropinosome; these subdomains are subsequently incorporated into highly dynamic, often branched, tubular structures. Time-lapse videomicroscopy revealed the highly dynamic extension of SNX5-labelled tubules and their departure from the macropinosome body to follow predefined paths towards the perinuclear region of the cell, before fusing with early endosomal acceptor membranes. The extension and departure of these tubular structures occurs rapidly over 5-10 minutes and is dependent upon intact microtubules. As the tubular structures depart from the macropinosome there is a reduction in the surface area and an increase in tension of the limiting membrane of the macropinosome. In addition to the recruitment of SNX5 to the macropinosome, Rab5, SNX1 and EEA1 are also recruited by newly formed macropinosomes, followed by the accumulation of Rab7. SNX5 forms heterodimers with SNX1 and this interaction is required for endosome association of SNX5. We propose that the departure of SNX5-positive tubules represents a rapid mechanism of recycling components from macropinosomes thereby promoting their maturation into Rab7-positive structures. Collectively these findings provide a detailed real-time characterisation of the maturation process of the macropinocytic endosome.
Key words: Sorting nexin, Macropinosome, Maturation, Endosomal trafficking
![]()
CiteULike
Complore
Connotea
Del.icio.us
Digg
Reddit
Technorati
Twitter What's this?
Related articles in JCS:
This article has been cited by other articles:
![]() |
C. Esk, C.-Y. Chen, L. Johannes, and F. M. Brodsky The clathrin heavy chain isoform CHC22 functions in a novel endosomal sorting step J. Cell Biol., January 11, 2010; 188(1): 131 - 144. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. M. I. Koharudin, W. Furey, H. Liu, Y.-J. Liu, and A. M. Gronenborn The Phox Domain of Sorting Nexin 5 Lacks Phosphatidylinositol 3-Phosphate (PtdIns(3)P) Specificity and Preferentially Binds to Phosphatidylinositol 4,5-Bisphosphate (PtdIns(4,5)P2) J. Biol. Chem., August 28, 2009; 284(35): 23697 - 23707. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Hara, E. Kiyokawa, S.-i. Iemura, T. Natsume, T. Wassmer, P. J. Cullen, H. Hiai, and M. Matsuda The DHR1 Domain of DOCK180 Binds to SNX5 and Regulates Cation-independent Mannose 6-phosphate Receptor Transport Mol. Biol. Cell, September 1, 2008; 19(9): 3823 - 3835. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. V. Bujny, P. A. Ewels, S. Humphrey, N. Attar, M. A. Jepson, and P. J. Cullen Sorting nexin-1 defines an early phase of Salmonella-containing vacuole-remodeling during Salmonella infection J. Cell Sci., June 15, 2008; 121(12): 2027 - 2036. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. V. Bujny, V. Popoff, L. Johannes, and P. J. Cullen The retromer component sorting nexin-1 is required for efficient retrograde transport of Shiga toxin from early endosome to the trans Golgi network J. Cell Sci., June 15, 2007; 120(12): 2010 - 2021. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. M. Bryant, M. C. Kerr, L. A. Hammond, S. R. Joseph, K. E. Mostov, R. D. Teasdale, and J. L. Stow EGF induces macropinocytosis and SNX1-modulated recycling of E-cadherin J. Cell Sci., May 15, 2007; 120(10): 1818 - 1828. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Wassmer, N. Attar, M. V. Bujny, J. Oakley, C. J. Traer, and P. J. Cullen A loss-of-function screen reveals SNX5 and SNX6 as potential components of the mammalian retromer J. Cell Sci., January 1, 2007; 120(1): 45 - 54. [Abstract] [Full Text] [PDF] |
||||