| Literature DB >> 35499795 |
Yan-Zhe Liao1, Jing Ma2, Jie-Zhi Dou3.
Abstract
In recent years, more and more neurodegenerative diseases, such as ALS, FTLD and AD, have been found to share a common pathological feature, which is the depletion of TDP-43 in the nucleus and the accumulation of TDP-43 in the cytoplasm through hyperphosphorylation, ubiquitination and cleavage. Therefore, this kind of neurodegenerative disease is also called TDP-43 proteinopathy. This suggests that TDP-43 plays a role in the pathogenesis of disease. Current studies show that the pathophysiological mechanism of TDP-43 in neurodegeneration is very complex. In this review, we describe the structure of TDP-43, its main physiological functions, the possible pathogenesis and how TDP-43 provides a new pathway to treat neurodegenerative diseases.Entities:
Keywords: Neurodegenerative disease; TDP-43; TDP-43 proteinopathy
Mesh:
Substances:
Year: 2022 PMID: 35499795 DOI: 10.1007/s12035-022-02847-x
Source DB: PubMed Journal: Mol Neurobiol ISSN: 0893-7648 Impact factor: 5.590