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Possible role of IRTKS in Tks5-driven osteoclast fusion

Podosomes and invadopodia seen in osteoclasts and cancer cells, respectively, are actin-rich membrane protrusions. We recently demonstrated that an adaptor protein, Tks5, which is an established regulator of invadopodia in cancer cells, drives osteoclast-osteoclast fusion as well as osteoclast-cance...

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Detalles Bibliográficos
Autores principales: Oikawa, Tsukasa, Matsuo, Koichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3502220/
https://www.ncbi.nlm.nih.gov/pubmed/23739834
http://dx.doi.org/10.4161/cib.21252
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author Oikawa, Tsukasa
Matsuo, Koichi
author_facet Oikawa, Tsukasa
Matsuo, Koichi
author_sort Oikawa, Tsukasa
collection PubMed
description Podosomes and invadopodia seen in osteoclasts and cancer cells, respectively, are actin-rich membrane protrusions. We recently demonstrated that an adaptor protein, Tks5, which is an established regulator of invadopodia in cancer cells, drives osteoclast-osteoclast fusion as well as osteoclast-cancer cell fusion by generating circumferential podosomes/invadopodia. This finding revealed an unexpected potential of podosomes/invadopodia to act as fusion-competent protrusions. Fusion of biological membranes involves the intricate orchestration of various proteins and lipids. Recent literature suggests the importance of membrane curvature formation in lipid bilayer fusion. In this study, we investigated the expression of Bin-Amphiphysin-Rvs161/167 (BAR) domain superfamily proteins, which have membrane deforming activity, during osteoclastogenesis. We found that IRTKS was specifically induced during osteoclast fusion and interacted with Tks5, suggesting the role of IRTKS in the formation of fusion-competent protrusions via its BAR domain.
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spelling pubmed-35022202012-11-23 Possible role of IRTKS in Tks5-driven osteoclast fusion Oikawa, Tsukasa Matsuo, Koichi Commun Integr Biol Article Addendum Podosomes and invadopodia seen in osteoclasts and cancer cells, respectively, are actin-rich membrane protrusions. We recently demonstrated that an adaptor protein, Tks5, which is an established regulator of invadopodia in cancer cells, drives osteoclast-osteoclast fusion as well as osteoclast-cancer cell fusion by generating circumferential podosomes/invadopodia. This finding revealed an unexpected potential of podosomes/invadopodia to act as fusion-competent protrusions. Fusion of biological membranes involves the intricate orchestration of various proteins and lipids. Recent literature suggests the importance of membrane curvature formation in lipid bilayer fusion. In this study, we investigated the expression of Bin-Amphiphysin-Rvs161/167 (BAR) domain superfamily proteins, which have membrane deforming activity, during osteoclastogenesis. We found that IRTKS was specifically induced during osteoclast fusion and interacted with Tks5, suggesting the role of IRTKS in the formation of fusion-competent protrusions via its BAR domain. Landes Bioscience 2012-09-01 /pmc/articles/PMC3502220/ /pubmed/23739834 http://dx.doi.org/10.4161/cib.21252 Text en Copyright © 2012 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Article Addendum
Oikawa, Tsukasa
Matsuo, Koichi
Possible role of IRTKS in Tks5-driven osteoclast fusion
title Possible role of IRTKS in Tks5-driven osteoclast fusion
title_full Possible role of IRTKS in Tks5-driven osteoclast fusion
title_fullStr Possible role of IRTKS in Tks5-driven osteoclast fusion
title_full_unstemmed Possible role of IRTKS in Tks5-driven osteoclast fusion
title_short Possible role of IRTKS in Tks5-driven osteoclast fusion
title_sort possible role of irtks in tks5-driven osteoclast fusion
topic Article Addendum
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3502220/
https://www.ncbi.nlm.nih.gov/pubmed/23739834
http://dx.doi.org/10.4161/cib.21252
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