Potential therapeutic manipulations of the CXCR3 chemokine axis for the treatment of inflammatory fibrosing diseases [version 1; peer review: 2 approved]

Chemokines play important roles in homeostasis and inflammatory processes. While their roles in leukocyte recruitment are well-appreciated, chemokines play additional roles in the body, including mediating or regulating angiogenesis, tumor metastasis and wound healing. In this opinion article, we fo...

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Main Authors: Morgan K. Groover, Jillian M. Richmond
Format: Article
Language:English
Published: F1000 Research Ltd 2020-10-01
Series:F1000Research
Online Access:https://f1000research.com/articles/9-1197/v1
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spelling doaj-c0c3a2cdce4247a4a3262d0b4e48e9682020-11-25T03:44:30ZengF1000 Research LtdF1000Research2046-14022020-10-01910.12688/f1000research.26728.129512Potential therapeutic manipulations of the CXCR3 chemokine axis for the treatment of inflammatory fibrosing diseases [version 1; peer review: 2 approved]Morgan K. Groover0Jillian M. Richmond1Department of Dermatology, University of Massachussetts Medical School, Worcester, MA, 01605, USADepartment of Dermatology, University of Massachussetts Medical School, Worcester, MA, 01605, USAChemokines play important roles in homeostasis and inflammatory processes. While their roles in leukocyte recruitment are well-appreciated, chemokines play additional roles in the body, including mediating or regulating angiogenesis, tumor metastasis and wound healing. In this opinion article, we focus on the role of CXCR3 and its ligands in fibrotic processes. We emphasize differences of the effects of each ligand, CXCL9, CXCL10 and CXCL11, on fibroblasts in different tissues of the body. We include discussions of differences in signaling pathways that may account for protective or pro-fibrotic effects of each ligand in different experimental models and ex vivo analysis of human tissues. Our goal is to highlight potential reasons why there are disparate findings in different models, and to suggest ways in which this chemokine axis could be manipulated for the treatment of fibrosis.https://f1000research.com/articles/9-1197/v1
collection DOAJ
language English
format Article
sources DOAJ
author Morgan K. Groover
Jillian M. Richmond
spellingShingle Morgan K. Groover
Jillian M. Richmond
Potential therapeutic manipulations of the CXCR3 chemokine axis for the treatment of inflammatory fibrosing diseases [version 1; peer review: 2 approved]
F1000Research
author_facet Morgan K. Groover
Jillian M. Richmond
author_sort Morgan K. Groover
title Potential therapeutic manipulations of the CXCR3 chemokine axis for the treatment of inflammatory fibrosing diseases [version 1; peer review: 2 approved]
title_short Potential therapeutic manipulations of the CXCR3 chemokine axis for the treatment of inflammatory fibrosing diseases [version 1; peer review: 2 approved]
title_full Potential therapeutic manipulations of the CXCR3 chemokine axis for the treatment of inflammatory fibrosing diseases [version 1; peer review: 2 approved]
title_fullStr Potential therapeutic manipulations of the CXCR3 chemokine axis for the treatment of inflammatory fibrosing diseases [version 1; peer review: 2 approved]
title_full_unstemmed Potential therapeutic manipulations of the CXCR3 chemokine axis for the treatment of inflammatory fibrosing diseases [version 1; peer review: 2 approved]
title_sort potential therapeutic manipulations of the cxcr3 chemokine axis for the treatment of inflammatory fibrosing diseases [version 1; peer review: 2 approved]
publisher F1000 Research Ltd
series F1000Research
issn 2046-1402
publishDate 2020-10-01
description Chemokines play important roles in homeostasis and inflammatory processes. While their roles in leukocyte recruitment are well-appreciated, chemokines play additional roles in the body, including mediating or regulating angiogenesis, tumor metastasis and wound healing. In this opinion article, we focus on the role of CXCR3 and its ligands in fibrotic processes. We emphasize differences of the effects of each ligand, CXCL9, CXCL10 and CXCL11, on fibroblasts in different tissues of the body. We include discussions of differences in signaling pathways that may account for protective or pro-fibrotic effects of each ligand in different experimental models and ex vivo analysis of human tissues. Our goal is to highlight potential reasons why there are disparate findings in different models, and to suggest ways in which this chemokine axis could be manipulated for the treatment of fibrosis.
url https://f1000research.com/articles/9-1197/v1
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AT jillianmrichmond potentialtherapeuticmanipulationsofthecxcr3chemokineaxisforthetreatmentofinflammatoryfibrosingdiseasesversion1peerreview2approved
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