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Disease Animal Models of TDP-43 Proteinopathy and Their Pre-Clinical Applications

Frontotemperal lobar degeneration (FTLD) and amyotrophic lateral sclerosis (ALS) are two common neurodegenerative diseases. TDP-43 is considered to be a major disease protein in FTLD/ALS, but it’s exact role in the pathogenesis and the effective treatments remains unknown. To address this question a...

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Autores principales: Liu, Yu-Chih, Chiang, Po-Min, Tsai, Kuen-Jer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3821604/
https://www.ncbi.nlm.nih.gov/pubmed/24113586
http://dx.doi.org/10.3390/ijms141020079
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author Liu, Yu-Chih
Chiang, Po-Min
Tsai, Kuen-Jer
author_facet Liu, Yu-Chih
Chiang, Po-Min
Tsai, Kuen-Jer
author_sort Liu, Yu-Chih
collection PubMed
description Frontotemperal lobar degeneration (FTLD) and amyotrophic lateral sclerosis (ALS) are two common neurodegenerative diseases. TDP-43 is considered to be a major disease protein in FTLD/ALS, but it’s exact role in the pathogenesis and the effective treatments remains unknown. To address this question and to determine a potential treatment for FTLD/ALS, the disease animal models of TDP-43 proteinopathy have been established. TDP-43 proteinopathy is the histologic feature of FTLD/ALS and is associated with disease progression. Studies on the disease animal models with TDP-43 proteinopathy and their pre-clinical applications are reviewed and summarized. Through these disease animal models, parts of TDP-43 functions in physiological and pathological conditions will be better understood and possible treatments for FTLD/ALS with TDP-43 proteinopathy may be identified for possible clinical applications in the future.
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spelling pubmed-38216042013-11-11 Disease Animal Models of TDP-43 Proteinopathy and Their Pre-Clinical Applications Liu, Yu-Chih Chiang, Po-Min Tsai, Kuen-Jer Int J Mol Sci Review Frontotemperal lobar degeneration (FTLD) and amyotrophic lateral sclerosis (ALS) are two common neurodegenerative diseases. TDP-43 is considered to be a major disease protein in FTLD/ALS, but it’s exact role in the pathogenesis and the effective treatments remains unknown. To address this question and to determine a potential treatment for FTLD/ALS, the disease animal models of TDP-43 proteinopathy have been established. TDP-43 proteinopathy is the histologic feature of FTLD/ALS and is associated with disease progression. Studies on the disease animal models with TDP-43 proteinopathy and their pre-clinical applications are reviewed and summarized. Through these disease animal models, parts of TDP-43 functions in physiological and pathological conditions will be better understood and possible treatments for FTLD/ALS with TDP-43 proteinopathy may be identified for possible clinical applications in the future. Molecular Diversity Preservation International (MDPI) 2013-10-09 /pmc/articles/PMC3821604/ /pubmed/24113586 http://dx.doi.org/10.3390/ijms141020079 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Liu, Yu-Chih
Chiang, Po-Min
Tsai, Kuen-Jer
Disease Animal Models of TDP-43 Proteinopathy and Their Pre-Clinical Applications
title Disease Animal Models of TDP-43 Proteinopathy and Their Pre-Clinical Applications
title_full Disease Animal Models of TDP-43 Proteinopathy and Their Pre-Clinical Applications
title_fullStr Disease Animal Models of TDP-43 Proteinopathy and Their Pre-Clinical Applications
title_full_unstemmed Disease Animal Models of TDP-43 Proteinopathy and Their Pre-Clinical Applications
title_short Disease Animal Models of TDP-43 Proteinopathy and Their Pre-Clinical Applications
title_sort disease animal models of tdp-43 proteinopathy and their pre-clinical applications
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3821604/
https://www.ncbi.nlm.nih.gov/pubmed/24113586
http://dx.doi.org/10.3390/ijms141020079
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