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CDNF Interacts with ER Chaperones and Requires UPR Sensors to Promote Neuronal Survival
Cerebral dopamine neurotrophic factor (CDNF) is a neurotrophic factor that has beneficial effects on dopamine neurons in both in vitro and in vivo models of Parkinson’s disease (PD). CDNF was recently tested in phase I-II clinical trials for the treatment of PD, but the mechanisms underlying its neu...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9408947/ https://www.ncbi.nlm.nih.gov/pubmed/36012764 http://dx.doi.org/10.3390/ijms23169489 |
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author | Eesmaa, Ave Yu, Li-Ying Göös, Helka Danilova, Tatiana Nõges, Kristofer Pakarinen, Emmi Varjosalo, Markku Lindahl, Maria Lindholm, Päivi Saarma, Mart |
author_facet | Eesmaa, Ave Yu, Li-Ying Göös, Helka Danilova, Tatiana Nõges, Kristofer Pakarinen, Emmi Varjosalo, Markku Lindahl, Maria Lindholm, Päivi Saarma, Mart |
author_sort | Eesmaa, Ave |
collection | PubMed |
description | Cerebral dopamine neurotrophic factor (CDNF) is a neurotrophic factor that has beneficial effects on dopamine neurons in both in vitro and in vivo models of Parkinson’s disease (PD). CDNF was recently tested in phase I-II clinical trials for the treatment of PD, but the mechanisms underlying its neuroprotective properties are still poorly understood, although studies have suggested its role in the regulation of endoplasmic reticulum (ER) homeostasis and the unfolded protein response (UPR). The aim of this study was to investigate the mechanism of action of CDNF through analyzing the involvement of UPR signaling in its anti-apoptotic function. We used tunicamycin to induce ER stress in mice in vivo and used cultured primary neurons and found that CDNF expression is regulated by ER stress in vivo and that the involvement of UPR pathways is important for the neuroprotective function of CDNF. Moreover, we used AP-MS and BiFC to perform the first interactome screening for CDNF and report novel binding partners of CDNF. These findings allowed us to hypothesize that CDNF protects neurons from ER-stress-inducing agents by modulating UPR signaling towards cell survival outcomes. |
format | Online Article Text |
id | pubmed-9408947 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-94089472022-08-26 CDNF Interacts with ER Chaperones and Requires UPR Sensors to Promote Neuronal Survival Eesmaa, Ave Yu, Li-Ying Göös, Helka Danilova, Tatiana Nõges, Kristofer Pakarinen, Emmi Varjosalo, Markku Lindahl, Maria Lindholm, Päivi Saarma, Mart Int J Mol Sci Article Cerebral dopamine neurotrophic factor (CDNF) is a neurotrophic factor that has beneficial effects on dopamine neurons in both in vitro and in vivo models of Parkinson’s disease (PD). CDNF was recently tested in phase I-II clinical trials for the treatment of PD, but the mechanisms underlying its neuroprotective properties are still poorly understood, although studies have suggested its role in the regulation of endoplasmic reticulum (ER) homeostasis and the unfolded protein response (UPR). The aim of this study was to investigate the mechanism of action of CDNF through analyzing the involvement of UPR signaling in its anti-apoptotic function. We used tunicamycin to induce ER stress in mice in vivo and used cultured primary neurons and found that CDNF expression is regulated by ER stress in vivo and that the involvement of UPR pathways is important for the neuroprotective function of CDNF. Moreover, we used AP-MS and BiFC to perform the first interactome screening for CDNF and report novel binding partners of CDNF. These findings allowed us to hypothesize that CDNF protects neurons from ER-stress-inducing agents by modulating UPR signaling towards cell survival outcomes. MDPI 2022-08-22 /pmc/articles/PMC9408947/ /pubmed/36012764 http://dx.doi.org/10.3390/ijms23169489 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Eesmaa, Ave Yu, Li-Ying Göös, Helka Danilova, Tatiana Nõges, Kristofer Pakarinen, Emmi Varjosalo, Markku Lindahl, Maria Lindholm, Päivi Saarma, Mart CDNF Interacts with ER Chaperones and Requires UPR Sensors to Promote Neuronal Survival |
title | CDNF Interacts with ER Chaperones and Requires UPR Sensors to Promote Neuronal Survival |
title_full | CDNF Interacts with ER Chaperones and Requires UPR Sensors to Promote Neuronal Survival |
title_fullStr | CDNF Interacts with ER Chaperones and Requires UPR Sensors to Promote Neuronal Survival |
title_full_unstemmed | CDNF Interacts with ER Chaperones and Requires UPR Sensors to Promote Neuronal Survival |
title_short | CDNF Interacts with ER Chaperones and Requires UPR Sensors to Promote Neuronal Survival |
title_sort | cdnf interacts with er chaperones and requires upr sensors to promote neuronal survival |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9408947/ https://www.ncbi.nlm.nih.gov/pubmed/36012764 http://dx.doi.org/10.3390/ijms23169489 |
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