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Probing the therapeutic potential of TRPC6 for Alzheimer’s disease in live neurons from patient-specific iPSCs
The induced pluripotent stem cells (iPSCs) offer an unprecedented opportunity to model and study Alzheimer’s disease (AD) under patient-specific genetic background. The lower expression of transient receptor potential canonical 6 (TRPC6) was associated with AD patients, which might be involved in AD...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7816687/ https://www.ncbi.nlm.nih.gov/pubmed/32492143 http://dx.doi.org/10.1093/jmcb/mjaa027 |
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author | Tao, Ran Lu, Rui Wang, Junfeng Zeng, Shujun Zhang, Ting Guo, Wenke Zhang, Xiaobing Cheng, Qi Yue, Chunmei Wang, Yizheng Jing, Naihe |
author_facet | Tao, Ran Lu, Rui Wang, Junfeng Zeng, Shujun Zhang, Ting Guo, Wenke Zhang, Xiaobing Cheng, Qi Yue, Chunmei Wang, Yizheng Jing, Naihe |
author_sort | Tao, Ran |
collection | PubMed |
description | The induced pluripotent stem cells (iPSCs) offer an unprecedented opportunity to model and study Alzheimer’s disease (AD) under patient-specific genetic background. The lower expression of transient receptor potential canonical 6 (TRPC6) was associated with AD patients, which might be involved in AD pathogenesis. However, the role of TRPC6 that played in AD process still needs more investigation in patient-relevant neurons. In this study, the iPSCs were generated from peripheral blood cells of sporadic AD patients and efficiently differentiated into mature cortical neurons. These sporadic AD-bearing neurons displayed higher levels of AD pathological markers Aβ and phospho-tau, but lower levels of TRPC6, than those of control neurons. Treatment of AD neurons with TRPC6 protein fragment or agonist inhibited the elevation of Aβ and phospho-tau. Our results in live AD neurons manifest that the compromised expression of TRPC6 substantially contributed to Aβ pathology of sporadic AD, suggesting that targeting TRPC6 could help to develop novel therapeutic strategies for the treatments of AD. |
format | Online Article Text |
id | pubmed-7816687 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-78166872021-01-26 Probing the therapeutic potential of TRPC6 for Alzheimer’s disease in live neurons from patient-specific iPSCs Tao, Ran Lu, Rui Wang, Junfeng Zeng, Shujun Zhang, Ting Guo, Wenke Zhang, Xiaobing Cheng, Qi Yue, Chunmei Wang, Yizheng Jing, Naihe J Mol Cell Biol Article The induced pluripotent stem cells (iPSCs) offer an unprecedented opportunity to model and study Alzheimer’s disease (AD) under patient-specific genetic background. The lower expression of transient receptor potential canonical 6 (TRPC6) was associated with AD patients, which might be involved in AD pathogenesis. However, the role of TRPC6 that played in AD process still needs more investigation in patient-relevant neurons. In this study, the iPSCs were generated from peripheral blood cells of sporadic AD patients and efficiently differentiated into mature cortical neurons. These sporadic AD-bearing neurons displayed higher levels of AD pathological markers Aβ and phospho-tau, but lower levels of TRPC6, than those of control neurons. Treatment of AD neurons with TRPC6 protein fragment or agonist inhibited the elevation of Aβ and phospho-tau. Our results in live AD neurons manifest that the compromised expression of TRPC6 substantially contributed to Aβ pathology of sporadic AD, suggesting that targeting TRPC6 could help to develop novel therapeutic strategies for the treatments of AD. Oxford University Press 2020-06-03 /pmc/articles/PMC7816687/ /pubmed/32492143 http://dx.doi.org/10.1093/jmcb/mjaa027 Text en © The Author(s) (2020). Published by Oxford University Press on behalf of Journal of Molecular Cell Biology, IBCB, SIBS, CAS. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Article Tao, Ran Lu, Rui Wang, Junfeng Zeng, Shujun Zhang, Ting Guo, Wenke Zhang, Xiaobing Cheng, Qi Yue, Chunmei Wang, Yizheng Jing, Naihe Probing the therapeutic potential of TRPC6 for Alzheimer’s disease in live neurons from patient-specific iPSCs |
title | Probing the therapeutic potential of TRPC6 for Alzheimer’s disease in live neurons from patient-specific iPSCs |
title_full | Probing the therapeutic potential of TRPC6 for Alzheimer’s disease in live neurons from patient-specific iPSCs |
title_fullStr | Probing the therapeutic potential of TRPC6 for Alzheimer’s disease in live neurons from patient-specific iPSCs |
title_full_unstemmed | Probing the therapeutic potential of TRPC6 for Alzheimer’s disease in live neurons from patient-specific iPSCs |
title_short | Probing the therapeutic potential of TRPC6 for Alzheimer’s disease in live neurons from patient-specific iPSCs |
title_sort | probing the therapeutic potential of trpc6 for alzheimer’s disease in live neurons from patient-specific ipscs |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7816687/ https://www.ncbi.nlm.nih.gov/pubmed/32492143 http://dx.doi.org/10.1093/jmcb/mjaa027 |
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