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Rab4 and cellubrevin define different early endosome populations on the pathway of transferrin receptor recycling.
Open accessAbstract
During receptor mediated endocytosis, at least a fraction of recycling cargo typically accumulates in a pericentriolar cluster of tubules and vesicles. However, it is not clear if these endosomal structures are biochemically distinct from the early endosomes from which they are derived. To better characterize this pericentriolar endosome population, we determined the distribution of two endogenous proteins known to be functionally involved in receptor recycling [Rab4, cellubrevin (Cbvn)] relative to the distribution of a recycling ligand [transferrin (Tfn)] as it traversed the endocytic pathway. Shortly after internalization, Tfn entered a population of early endosomes that contained both Rab4 and Cbvn, demonstrated by triple label immunofluorescence confocal microscopy. Tfn then accumulated in the pericentriolar cluster of recycling vesicles (RVs). However, although these pericentriolar endosomes contained Cbvn, they were strikingly depleted of Rab4. The ability of internalized Tfn to reach the Rab4-negative population was not blocked by nocodazole, although the characteristic pericentriolar location of the population was not maintained in the absence of microtubules. Similarly, Rab4-positive and -negative populations remained distinct in cells treated with brefeldin A, with only Rab4-positive elements exhibiting the extended tubular morphology induced by the drug. Thus, at least with respect to Rab4 distribution, the pathway of Tfn receptor recycling consists of at least two biochemically and functionally distinct populations of endosomes, a Rab4-positive population of early endosomes to which incoming Tfn is initially delivered and a Rab4-negative population of recycling vesicles that transiently accumulates Tfn on its route back to the plasma membrane.
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“Expression of dominant-negative Rab11 has been shown to specifically inhibit transferrin receptor recycling (Daro et al., 1996;Ren et al., 1998).”
From BDNF-Dependent Recycling Facilitates TrkB Translocation to Postsynaptic Density during LTP via a Rab11-Dependent Pathway (2013) · cites this paper as Daro et al., 1996
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Metadata
- Authors
- Daro, E., van der Sluijs, P., Galli, T., & Mellman, I.
- Affiliations
- Yale University (US)
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 1996-09-03
- Volume
- 93
- Issue
- 18
- Pages
- 9559-9564
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC38467
- OpenAlex
- W2018435413
- Cited by
- 343
- References
- 35
- Citations by year
- 2026: 2 · 2025: 4 · 2024: 4 · 2023: 8 · 2022: 10 · 2021: 7 · 2020: 6 · 2019: 4 · 2018: 5 · 2017: 4 · 2016: 11 · 2015: 11 · 2014: 10 · 2013: 13 · 2012: 10
- FWCI
- 4.75
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Physiology › Calcium signaling and nucleotide metabolism
- Keywords
- Rab4, cellubrevin, early endosomes, transferrin receptor recycling, receptor-mediated endocytosis, microtubules, brefeldin A, nocodazole
- MeSH terms
- Animals, Cell Compartmentation, Cell Line, Cell Membrane, Cricetulus, Cyclopentanes, Cricetinae, Humans, Kinetics, Membrane Proteins, Receptors, Transferrin, Endosomes, Nocodazole, Fluorescein-5-isothiocyanate, Microscopy, Confocal, Fluorescent Antibody Technique, Direct, GTP-Binding Proteins, Brefeldin A, rab4 GTP-Binding Proteins, Vesicle-Associated Membrane Protein 3
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