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Involvement of CXCR4/CXCR7/CXCL12 Interactions in Inflammatory Bowel Disease
Directional movement of cells in the human body is orchestrated via chemokines. This migration was initially identified in pathological and immunological processes but quickly extended to homeostatic cell trafficking. One such chemokine is the ubiquitous CXCL12 (initially called SDF1-α) which signal...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2013
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3563080/ https://www.ncbi.nlm.nih.gov/pubmed/23382785 http://dx.doi.org/10.7150/thno.5135 |
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author | Werner, Lael Guzner-Gur, Hanan Dotan, Iris |
author_facet | Werner, Lael Guzner-Gur, Hanan Dotan, Iris |
author_sort | Werner, Lael |
collection | PubMed |
description | Directional movement of cells in the human body is orchestrated via chemokines. This migration was initially identified in pathological and immunological processes but quickly extended to homeostatic cell trafficking. One such chemokine is the ubiquitous CXCL12 (initially called SDF1-α) which signals via the chemokine receptors CXCR4 and CXCR7. In the last decade CXCL12 was recognized to participate not only in embryonic development and homeostatic maintenance, but also in progression of inflammation. A role for CXCL12 and its receptors CXCR4 and CXCR7 in inflammatory bowel diseases was recently shown. The current review discusses up to date knowledge of CXCL12 in inflammation, focusing on the involvement of CXCL12 and its receptors, CXCR4 and CXCR7, in inflammatory bowel diseases. |
format | Online Article Text |
id | pubmed-3563080 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-35630802013-02-04 Involvement of CXCR4/CXCR7/CXCL12 Interactions in Inflammatory Bowel Disease Werner, Lael Guzner-Gur, Hanan Dotan, Iris Theranostics Review Directional movement of cells in the human body is orchestrated via chemokines. This migration was initially identified in pathological and immunological processes but quickly extended to homeostatic cell trafficking. One such chemokine is the ubiquitous CXCL12 (initially called SDF1-α) which signals via the chemokine receptors CXCR4 and CXCR7. In the last decade CXCL12 was recognized to participate not only in embryonic development and homeostatic maintenance, but also in progression of inflammation. A role for CXCL12 and its receptors CXCR4 and CXCR7 in inflammatory bowel diseases was recently shown. The current review discusses up to date knowledge of CXCL12 in inflammation, focusing on the involvement of CXCL12 and its receptors, CXCR4 and CXCR7, in inflammatory bowel diseases. Ivyspring International Publisher 2013-01-15 /pmc/articles/PMC3563080/ /pubmed/23382785 http://dx.doi.org/10.7150/thno.5135 Text en © Ivyspring International Publisher. This is an open-access article distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by-nc-nd/3.0/). Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited. |
spellingShingle | Review Werner, Lael Guzner-Gur, Hanan Dotan, Iris Involvement of CXCR4/CXCR7/CXCL12 Interactions in Inflammatory Bowel Disease |
title | Involvement of CXCR4/CXCR7/CXCL12 Interactions in Inflammatory Bowel Disease |
title_full | Involvement of CXCR4/CXCR7/CXCL12 Interactions in Inflammatory Bowel Disease |
title_fullStr | Involvement of CXCR4/CXCR7/CXCL12 Interactions in Inflammatory Bowel Disease |
title_full_unstemmed | Involvement of CXCR4/CXCR7/CXCL12 Interactions in Inflammatory Bowel Disease |
title_short | Involvement of CXCR4/CXCR7/CXCL12 Interactions in Inflammatory Bowel Disease |
title_sort | involvement of cxcr4/cxcr7/cxcl12 interactions in inflammatory bowel disease |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3563080/ https://www.ncbi.nlm.nih.gov/pubmed/23382785 http://dx.doi.org/10.7150/thno.5135 |
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