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Microglia, seen from the CX(3)CR1 angle

Microglial cells in brain and spinal cord are characterized by high expression of the chemokine receptor CX(3)CR1. Expression of the sole CX(3)CR1 ligand, the membrane-tethered and sheddable chemokine CX(3)CL1/fractalkine, is restricted in the brain parenchyma to selected neurons. Here we summarize...

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Detalles Bibliográficos
Autores principales: Wolf, Yochai, Yona, Simon, Kim, Ki-Wook, Jung, Steffen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3600435/
https://www.ncbi.nlm.nih.gov/pubmed/23507975
http://dx.doi.org/10.3389/fncel.2013.00026
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author Wolf, Yochai
Yona, Simon
Kim, Ki-Wook
Jung, Steffen
author_facet Wolf, Yochai
Yona, Simon
Kim, Ki-Wook
Jung, Steffen
author_sort Wolf, Yochai
collection PubMed
description Microglial cells in brain and spinal cord are characterized by high expression of the chemokine receptor CX(3)CR1. Expression of the sole CX(3)CR1 ligand, the membrane-tethered and sheddable chemokine CX(3)CL1/fractalkine, is restricted in the brain parenchyma to selected neurons. Here we summarize our current understanding of the physiological role of CX(3)CR1 for microglia function and the CX(3)C axis in microglial/neuronal crosstalk in homeostasis and under challenge. Moreover, we will discuss the efforts of our laboratory and others to exploit CX(3)CR1 promoter activity for the visualization and genetic manipulation of microglia to probe their functional contributions in the central nerve system (CNS) context.
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spelling pubmed-36004352013-03-18 Microglia, seen from the CX(3)CR1 angle Wolf, Yochai Yona, Simon Kim, Ki-Wook Jung, Steffen Front Cell Neurosci Neuroscience Microglial cells in brain and spinal cord are characterized by high expression of the chemokine receptor CX(3)CR1. Expression of the sole CX(3)CR1 ligand, the membrane-tethered and sheddable chemokine CX(3)CL1/fractalkine, is restricted in the brain parenchyma to selected neurons. Here we summarize our current understanding of the physiological role of CX(3)CR1 for microglia function and the CX(3)C axis in microglial/neuronal crosstalk in homeostasis and under challenge. Moreover, we will discuss the efforts of our laboratory and others to exploit CX(3)CR1 promoter activity for the visualization and genetic manipulation of microglia to probe their functional contributions in the central nerve system (CNS) context. Frontiers Media S.A. 2013-03-18 /pmc/articles/PMC3600435/ /pubmed/23507975 http://dx.doi.org/10.3389/fncel.2013.00026 Text en Copyright © 2013 Wolf, Yona, Kim and Jung. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Neuroscience
Wolf, Yochai
Yona, Simon
Kim, Ki-Wook
Jung, Steffen
Microglia, seen from the CX(3)CR1 angle
title Microglia, seen from the CX(3)CR1 angle
title_full Microglia, seen from the CX(3)CR1 angle
title_fullStr Microglia, seen from the CX(3)CR1 angle
title_full_unstemmed Microglia, seen from the CX(3)CR1 angle
title_short Microglia, seen from the CX(3)CR1 angle
title_sort microglia, seen from the cx(3)cr1 angle
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3600435/
https://www.ncbi.nlm.nih.gov/pubmed/23507975
http://dx.doi.org/10.3389/fncel.2013.00026
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