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NRP1 function and targeting in neurovascular development and eye disease
Neuropilin 1 (NRP1) is expressed by neurons, blood vessels, immune cells and many other cell types in the mammalian body and binds a range of structurally and functionally diverse extracellular ligands to modulate organ development and function. In recent years, several types of mouse knockout model...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Pergamon
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4854174/ https://www.ncbi.nlm.nih.gov/pubmed/26923176 http://dx.doi.org/10.1016/j.preteyeres.2016.02.003 |
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author | Raimondi, Claudio Brash, James T. Fantin, Alessandro Ruhrberg, Christiana |
author_facet | Raimondi, Claudio Brash, James T. Fantin, Alessandro Ruhrberg, Christiana |
author_sort | Raimondi, Claudio |
collection | PubMed |
description | Neuropilin 1 (NRP1) is expressed by neurons, blood vessels, immune cells and many other cell types in the mammalian body and binds a range of structurally and functionally diverse extracellular ligands to modulate organ development and function. In recent years, several types of mouse knockout models have been developed that have provided useful tools for experimental investigation of NRP1 function, and a multitude of therapeutics targeting NRP1 have been designed, mostly with the view to explore them for cancer treatment. This review provides a general overview of current knowledge of the signalling pathways that are modulated by NRP1, with particular focus on neuronal and vascular roles in the brain and retina. This review will also discuss the potential of NRP1 inhibitors for the treatment for neovascular eye diseases. |
format | Online Article Text |
id | pubmed-4854174 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Pergamon |
record_format | MEDLINE/PubMed |
spelling | pubmed-48541742016-05-10 NRP1 function and targeting in neurovascular development and eye disease Raimondi, Claudio Brash, James T. Fantin, Alessandro Ruhrberg, Christiana Prog Retin Eye Res Article Neuropilin 1 (NRP1) is expressed by neurons, blood vessels, immune cells and many other cell types in the mammalian body and binds a range of structurally and functionally diverse extracellular ligands to modulate organ development and function. In recent years, several types of mouse knockout models have been developed that have provided useful tools for experimental investigation of NRP1 function, and a multitude of therapeutics targeting NRP1 have been designed, mostly with the view to explore them for cancer treatment. This review provides a general overview of current knowledge of the signalling pathways that are modulated by NRP1, with particular focus on neuronal and vascular roles in the brain and retina. This review will also discuss the potential of NRP1 inhibitors for the treatment for neovascular eye diseases. Pergamon 2016-05 /pmc/articles/PMC4854174/ /pubmed/26923176 http://dx.doi.org/10.1016/j.preteyeres.2016.02.003 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Raimondi, Claudio Brash, James T. Fantin, Alessandro Ruhrberg, Christiana NRP1 function and targeting in neurovascular development and eye disease |
title | NRP1 function and targeting in neurovascular development and eye disease |
title_full | NRP1 function and targeting in neurovascular development and eye disease |
title_fullStr | NRP1 function and targeting in neurovascular development and eye disease |
title_full_unstemmed | NRP1 function and targeting in neurovascular development and eye disease |
title_short | NRP1 function and targeting in neurovascular development and eye disease |
title_sort | nrp1 function and targeting in neurovascular development and eye disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4854174/ https://www.ncbi.nlm.nih.gov/pubmed/26923176 http://dx.doi.org/10.1016/j.preteyeres.2016.02.003 |
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