Literature DB >> 9410882

Microtubule depolymerization inhibits clathrin coated-pit internalization in non-adherent cell lines while interleukin 2 endocytosis is not affected.

A Subtil1, A Dautry-Varsat.   

Abstract

The microtubule cytoskeleton is generally not considered to be essential for the first steps of clathrin-mediated endocytosis of membrane receptors. Its role in clathrin-independent endocytosis has not been investigated. We have previously shown that the cytokine interleukin 2 (IL2) is internalized in lymphoid cells expressing its receptors when clathrin-dependent endocytosis is inhibited. Here we compare the internalization of IL2 and of transferrin, a marker of clathrin-dependent endocytosis, after microtubule disruption. In hemopoietic cell lines, which express IL2 receptors, transferrin receptor entry was inhibited by about 40%. However, in adherent cell lines, transferrin entry was unaffected by microtubule disruption, as previously reported. Unlike the case for transferrin, internalization of IL2 receptors was not affected by depolymerization of the microtubule cytoskeleton in hemopoietic cell lines. These results show that IL2 and transferrin receptors do not have the same endocytic properties and support our previous conclusion that these receptors follow different pathways of endocytosis.

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Year:  1997        PMID: 9410882     DOI: 10.1242/jcs.110.19.2441

Source DB:  PubMed          Journal:  J Cell Sci        ISSN: 0021-9533            Impact factor:   5.285


  11 in total

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3.  Cellular internalization of quantum dots noncovalently conjugated with arginine-rich cell-penetrating peptides.

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Review 4.  Endocytosis of gene delivery vectors: from clathrin-dependent to lipid raft-mediated endocytosis.

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5.  Microtubule-mediated Src tyrosine kinase trafficking in neuronal growth cones.

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Review 6.  Mitotic inhibition of clathrin-mediated endocytosis.

Authors:  Andrew B Fielding; Stephen J Royle
Journal:  Cell Mol Life Sci       Date:  2013-01-11       Impact factor: 9.261

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8.  Differential compartmentalization of BMP4/NOGGIN requires NOGGIN trans-epithelial transport.

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Journal:  Nat Commun       Date:  2016-10-10       Impact factor: 14.919

10.  Self-Targeting of Carbon Dots into the Cell Nucleus: Diverse Mechanisms of Toxicity in NIH/3T3 and L929 Cells.

Authors:  Markéta Havrdová; Iztok Urbančič; Kateřina Bartoň Tománková; Lukáš Malina; Janez Štrancar; Athanasios B Bourlinos
Journal:  Int J Mol Sci       Date:  2021-05-25       Impact factor: 5.923

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