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Cited by 408

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Endocytic Traffic in Polarized Epithelial Cells: Role of the Actin and Microtubule Cytoskeleton

Apodaca, Gerard·2001·Traffic

Abstract

The cytoskeleton is required for multiple cellular events including endocytosis and the transfer of cargo within the endocytic system. Polarized epithelial cells are capable of endocytosis at either of their distinct apical or basolateral plasma membrane domains. Actin plays a role in internalization at both cell surfaces. Microtubules and actin are required for efficient transcytosis and delivery of proteins to late endosomes and lysosomes. Microtubules are also important in apical recycling pathways and, in some polarized cell types, basolateral recycling requires actin. The microtubule motor proteins dynein and kinesin and the class I unconventional myosin motors play a role in many of these trafficking steps. This review examines the endocytic pathways of polarized epithelial cells and focuses on the emerging roles of the actin cytoskeleton in these processes.

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Crossref · 10.1034/j.1600-0854.2001.020301.x

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Metadata

Authors
Apodaca, G.
Venue
Traffic
Publisher
Wiley
Published
2001-03
Volume
2
Issue
3
Pages
149-159
ISSN
  • 1398-9219 (ISSN-L)
  • 1600-0854
OpenAlex
W1536788210
Cited by
408
References
1
FWCI
10.55
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Endocytic Traffic in Polarized Epithelial Cells: Role of the Actin and Microtubule Cytoskeleton. https://app.cochat.ai/papers/10.1034/j.1600-0854.2001.020301.x
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Apodaca, G. (2001). Endocytic Traffic in Polarized Epithelial Cells: Role of the Actin and Microtubule Cytoskeleton. Traffic. https://doi.org/10.1034/j.1600-0854.2001.020301.x

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.