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The Many Faces of FKBP51
The FK506-binding protein 51 (FKBP51) has emerged as a key regulator of endocrine stress responses in mammals and as a potential therapeutic target for stress-related disorders (depression, post-traumatic stress disorder), metabolic disorders (obesity and diabetes) and chronic pain. Recently, FKBP51...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6359276/ https://www.ncbi.nlm.nih.gov/pubmed/30669684 http://dx.doi.org/10.3390/biom9010035 |
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author | Hähle, Andreas Merz, Stephanie Meyners, Christian Hausch, Felix |
author_facet | Hähle, Andreas Merz, Stephanie Meyners, Christian Hausch, Felix |
author_sort | Hähle, Andreas |
collection | PubMed |
description | The FK506-binding protein 51 (FKBP51) has emerged as a key regulator of endocrine stress responses in mammals and as a potential therapeutic target for stress-related disorders (depression, post-traumatic stress disorder), metabolic disorders (obesity and diabetes) and chronic pain. Recently, FKBP51 has been implicated in several cellular pathways and numerous interacting protein partners have been reported. However, no consensus on the underlying molecular mechanisms has yet emerged. Here, we review the protein interaction partners reported for FKBP51, the proposed pathways involved, their relevance to FKBP51’s physiological function(s), the interplay with other FKBPs, and implications for the development of FKBP51-directed drugs. |
format | Online Article Text |
id | pubmed-6359276 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-63592762019-02-11 The Many Faces of FKBP51 Hähle, Andreas Merz, Stephanie Meyners, Christian Hausch, Felix Biomolecules Review The FK506-binding protein 51 (FKBP51) has emerged as a key regulator of endocrine stress responses in mammals and as a potential therapeutic target for stress-related disorders (depression, post-traumatic stress disorder), metabolic disorders (obesity and diabetes) and chronic pain. Recently, FKBP51 has been implicated in several cellular pathways and numerous interacting protein partners have been reported. However, no consensus on the underlying molecular mechanisms has yet emerged. Here, we review the protein interaction partners reported for FKBP51, the proposed pathways involved, their relevance to FKBP51’s physiological function(s), the interplay with other FKBPs, and implications for the development of FKBP51-directed drugs. MDPI 2019-01-21 /pmc/articles/PMC6359276/ /pubmed/30669684 http://dx.doi.org/10.3390/biom9010035 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Hähle, Andreas Merz, Stephanie Meyners, Christian Hausch, Felix The Many Faces of FKBP51 |
title | The Many Faces of FKBP51 |
title_full | The Many Faces of FKBP51 |
title_fullStr | The Many Faces of FKBP51 |
title_full_unstemmed | The Many Faces of FKBP51 |
title_short | The Many Faces of FKBP51 |
title_sort | many faces of fkbp51 |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6359276/ https://www.ncbi.nlm.nih.gov/pubmed/30669684 http://dx.doi.org/10.3390/biom9010035 |
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