Abnormal interaction of Rlip with mutant APP/Abeta and phosphorylated tau reduces wild-type Rlip levels and disrupt Rlip function in Alzheimer's disease

被引:6
作者
Baig, Javaria [1 ]
Sawant, Neha [1 ]
Rawat, Priyanka [1 ]
Reddy, Arubala P. [2 ]
Reddy, P. Hemachandra [1 ,2 ,3 ,4 ,5 ,6 ,7 ]
Kshirsagar, Sudhir [1 ,7 ]
机构
[1] Texas Tech Univ, Hlth Sci Ctr, Dept Internal Med, Lubbock, TX 79430 USA
[2] Texas Tech Univ, Coll Human Sci, Dept Nutr Sci, 1301 Akron Ave, Lubbock, TX 79409 USA
[3] Texas Tech Univ, Hlth Sci Ctr, Dept Sch Med, Neurol, Lubbock, TX 79430 USA
[4] Texas Tech Univ, Hlth Sci Ctr, Grad Sch Biomed Sci, Publ Hlth Dept, Lubbock, TX 79430 USA
[5] Texas Tech Univ, Hlth Sci Ctr, Sch Hlth Profess, Dept Speech Language & Hearing Sci, Lubbock, TX 79430 USA
[6] Texas Tech Univ, Hlth Sci Ctr, Dept Pharmacol & Neurosci, Lubbock, TX 79430 USA
[7] Texas Tech Univ, Hlth Sci Ctr, Sch Med, Dept Internal Med, Lubbock, TX 79430 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 2024年 / 1870卷 / 01期
关键词
Alzheimer's disease; Rlip protein; Mitochondrial dysfunction; Oxidative stress;
D O I
10.1016/j.bbadis.2023.166858
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Alzheimer's disease (AD) is a neurodegenerative disease that affects a large proportion of the aging population. RalBP1 (Rlip) is a stress-activated protein, that plays an important role in aging and neurodegenerative diseases such as Alzheimer's disease. Mutant APP and mutant Tau interact with the Rlip protein which leads to decreased wild-type Rlip levels and disrupt Rlip function in Alzheimer's disease. Rlip is a promising new target for aging, Alzheimer's disease, and other neurological diseases.
引用
收藏
页数:3
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