Neutralizing peripheral circulating IL1β slows the progression of ALS in a lentivirus‐infected OPTNE478G mouse model
Abstract Background Amyotrophic lateral sclerosis (ALS) is irreversible and fatal within 3–5 years, with limited options for treatment. It is imperative to develop a symptom‐based treatment that may increase the survival of ALS patients and improve their quality of life. Inflammation status, especia...
Main Authors: | Wen‐Bao Hu, Xin Wang, Zhi‐Lin Pang, Ran Duan, Chun‐Gu Hong, Zheng‐Zhao Liu |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2023-02-01
|
Series: | Animal Models and Experimental Medicine |
Subjects: | |
Online Access: | https://doi.org/10.1002/ame2.12297 |
Similar Items
-
Optineurin Deficiency and Insufficiency Lead to Higher Microglial TDP-43 Protein Levels
by: Nikolina Prtenjaca, et al.
Published: (2022-06-01) -
Fundamental roles of the Optineurin gene in the molecular pathology of Amyotrophic Lateral Sclerosis
by: Shumin Zhao, et al.
Published: (2023-12-01) -
Dysfunction of Optineurin in Amyotrophic Lateral Sclerosis and Glaucoma
by: Reka P. Toth, et al.
Published: (2018-05-01) -
ALS-Related Mutant SOD1 Aggregates Interfere with Mitophagy by Sequestering the Autophagy Receptor Optineurin
by: Yeong Jin Tak, et al.
Published: (2020-10-01) -
β-N-Methylamino-L-Alanine Induces Neurological Deficits and Shortened Life Span in Drosophila
by: R. Grace Zhai, et al.
Published: (2010-11-01)