Abstract
Efficient post-Golgi trafficking depends on microtubules, but actin filaments and actin-associated proteins are also postulated. Here we examined, by inverse fluorescence recovery after photobleaching, the role of actin dynamics in the exit from the TGN of fluorescent-tagged apical or basolateral and raft or non-raft-associated cargoes. Either the actin-stabilizing jasplakinolide or the actin-depolymerising latrunculin B variably but significantly inhibited post-Golgi traffic of non-raft associated apical p75NTR and basolateral VSV-G cargoes. The TGN-exit of the apical-destined VSV-G mutant was impaired only by latrunculin B. Strikingly, the raft-associated GPI-anchor protein was not affected by either actin toxin. Results indicate that actin dynamics participates in the TGN egress of both apical- and basolateral-targeted proteins but is not needed for apical raft-associated cargo.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 3875-3881 |
| Number of pages | 7 |
| Journal | FEBS Letters |
| Volume | 581 |
| Issue number | 20 |
| DOIs | |
| State | Published - Aug 7 2007 |
| Externally published | Yes |
Keywords
- Actin
- Cytoskeleton
- Golgi apparatus
- Polarized transport
- Raft
- iFRAP
ASJC Scopus subject areas
- Biophysics
- Structural Biology
- Biochemistry
- Molecular Biology
- Genetics
- Cell Biology
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