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Discoidin domain receptors: Microenvironment sensors that promote cellular migration and invasion

Extracellular matrix (ECM) provides cells scaffolding for cell migration and microenvironment for various cellular functions. Collagens are major ECM components in tissue and discoidin domain receptors (DDRs) are receptor tyrosine kinases (RTK) that recognise fibrillar collagens. Unlike other RTK, t...

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Detalles Bibliográficos
Autor principal: Itoh, Yoshifumi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6363040/
https://www.ncbi.nlm.nih.gov/pubmed/29671358
http://dx.doi.org/10.1080/19336918.2018.1460011
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author Itoh, Yoshifumi
author_facet Itoh, Yoshifumi
author_sort Itoh, Yoshifumi
collection PubMed
description Extracellular matrix (ECM) provides cells scaffolding for cell migration and microenvironment for various cellular functions. Collagens are major ECM components in tissue and discoidin domain receptors (DDRs) are receptor tyrosine kinases (RTK) that recognise fibrillar collagens. Unlike other RTK, their ligands are solid ECM the that are abundantly present in the pericellular environment in various tissue, and thus its activation and regulations are unique amongst RTK family. It is emerging that DDRs may be the sensors that monitor and detects changes in ECM microenvironment and determines the cellular fates upon tissue injuries. In this mini-review, recent findings on the role of DDRs as microenvironment sensor and their roles in cell migration and invasion are discussed.
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spelling pubmed-63630402019-03-15 Discoidin domain receptors: Microenvironment sensors that promote cellular migration and invasion Itoh, Yoshifumi Cell Adh Migr Commentary Extracellular matrix (ECM) provides cells scaffolding for cell migration and microenvironment for various cellular functions. Collagens are major ECM components in tissue and discoidin domain receptors (DDRs) are receptor tyrosine kinases (RTK) that recognise fibrillar collagens. Unlike other RTK, their ligands are solid ECM the that are abundantly present in the pericellular environment in various tissue, and thus its activation and regulations are unique amongst RTK family. It is emerging that DDRs may be the sensors that monitor and detects changes in ECM microenvironment and determines the cellular fates upon tissue injuries. In this mini-review, recent findings on the role of DDRs as microenvironment sensor and their roles in cell migration and invasion are discussed. Taylor & Francis 2018-05-08 /pmc/articles/PMC6363040/ /pubmed/29671358 http://dx.doi.org/10.1080/19336918.2018.1460011 Text en © 2018 The Author(s). Published with license by Taylor & Francis Group http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
spellingShingle Commentary
Itoh, Yoshifumi
Discoidin domain receptors: Microenvironment sensors that promote cellular migration and invasion
title Discoidin domain receptors: Microenvironment sensors that promote cellular migration and invasion
title_full Discoidin domain receptors: Microenvironment sensors that promote cellular migration and invasion
title_fullStr Discoidin domain receptors: Microenvironment sensors that promote cellular migration and invasion
title_full_unstemmed Discoidin domain receptors: Microenvironment sensors that promote cellular migration and invasion
title_short Discoidin domain receptors: Microenvironment sensors that promote cellular migration and invasion
title_sort discoidin domain receptors: microenvironment sensors that promote cellular migration and invasion
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6363040/
https://www.ncbi.nlm.nih.gov/pubmed/29671358
http://dx.doi.org/10.1080/19336918.2018.1460011
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