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Targeting TNFR2 as a Novel Therapeutic Strategy for Alzheimer’s Disease
Alzheimer’s disease (AD) is a progressive neurodegenerative disorder and the most common cause of dementia. Accumulating experimental evidence shows the important linkage between tumor necrosis factor-α (TNF) and AD, but the exact role of TNF in AD is still not completely understood. Although TNF-in...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6369349/ https://www.ncbi.nlm.nih.gov/pubmed/30778285 http://dx.doi.org/10.3389/fnins.2019.00049 |
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author | Ortí-Casañ, Natalia Wu, Yingying Naudé, Petrus J. W. De Deyn, Peter P. Zuhorn, Inge S. Eisel, Ulrich L. M. |
author_facet | Ortí-Casañ, Natalia Wu, Yingying Naudé, Petrus J. W. De Deyn, Peter P. Zuhorn, Inge S. Eisel, Ulrich L. M. |
author_sort | Ortí-Casañ, Natalia |
collection | PubMed |
description | Alzheimer’s disease (AD) is a progressive neurodegenerative disorder and the most common cause of dementia. Accumulating experimental evidence shows the important linkage between tumor necrosis factor-α (TNF) and AD, but the exact role of TNF in AD is still not completely understood. Although TNF-inhibitors are successfully used for treating several diseases, total inhibition of TNF can cause side effects, particularly in neurological diseases. This is attributed to the opposing roles of the two TNF receptors. TNF receptor 1 (TNFR1) predominantly mediates inflammatory and pro-apoptotic signaling pathways, whereas TNF receptor 2 (TNFR2) is neuroprotective and promotes tissue regeneration. Therefore, the specific activation of TNFR2 signaling, either by directly targeting TNFR2 via TNFR2 agonists or by blocking TNFR1 signaling with TNFR1-selective antagonists, seems a promising strategy for AD therapy. This mini-review discusses the involvement of TNFR2 and its signaling pathway in AD and outlines its potential application as therapeutic target. A better understanding of the function of TNFR2 may lead to the development of a treatment for AD. |
format | Online Article Text |
id | pubmed-6369349 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63693492019-02-18 Targeting TNFR2 as a Novel Therapeutic Strategy for Alzheimer’s Disease Ortí-Casañ, Natalia Wu, Yingying Naudé, Petrus J. W. De Deyn, Peter P. Zuhorn, Inge S. Eisel, Ulrich L. M. Front Neurosci Neuroscience Alzheimer’s disease (AD) is a progressive neurodegenerative disorder and the most common cause of dementia. Accumulating experimental evidence shows the important linkage between tumor necrosis factor-α (TNF) and AD, but the exact role of TNF in AD is still not completely understood. Although TNF-inhibitors are successfully used for treating several diseases, total inhibition of TNF can cause side effects, particularly in neurological diseases. This is attributed to the opposing roles of the two TNF receptors. TNF receptor 1 (TNFR1) predominantly mediates inflammatory and pro-apoptotic signaling pathways, whereas TNF receptor 2 (TNFR2) is neuroprotective and promotes tissue regeneration. Therefore, the specific activation of TNFR2 signaling, either by directly targeting TNFR2 via TNFR2 agonists or by blocking TNFR1 signaling with TNFR1-selective antagonists, seems a promising strategy for AD therapy. This mini-review discusses the involvement of TNFR2 and its signaling pathway in AD and outlines its potential application as therapeutic target. A better understanding of the function of TNFR2 may lead to the development of a treatment for AD. Frontiers Media S.A. 2019-02-04 /pmc/articles/PMC6369349/ /pubmed/30778285 http://dx.doi.org/10.3389/fnins.2019.00049 Text en Copyright © 2019 Ortí-Casañ, Wu, Naudé, De Deyn, Zuhorn and Eisel. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Ortí-Casañ, Natalia Wu, Yingying Naudé, Petrus J. W. De Deyn, Peter P. Zuhorn, Inge S. Eisel, Ulrich L. M. Targeting TNFR2 as a Novel Therapeutic Strategy for Alzheimer’s Disease |
title | Targeting TNFR2 as a Novel Therapeutic Strategy for Alzheimer’s Disease |
title_full | Targeting TNFR2 as a Novel Therapeutic Strategy for Alzheimer’s Disease |
title_fullStr | Targeting TNFR2 as a Novel Therapeutic Strategy for Alzheimer’s Disease |
title_full_unstemmed | Targeting TNFR2 as a Novel Therapeutic Strategy for Alzheimer’s Disease |
title_short | Targeting TNFR2 as a Novel Therapeutic Strategy for Alzheimer’s Disease |
title_sort | targeting tnfr2 as a novel therapeutic strategy for alzheimer’s disease |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6369349/ https://www.ncbi.nlm.nih.gov/pubmed/30778285 http://dx.doi.org/10.3389/fnins.2019.00049 |
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