The role of RLIP76 in oxidative stress and mitochondrial dysfunction: Evidence based on autopsy brains from Alzheimer's disease patients

Several converging lines of evidence from our group support a potential role of RLIP76 (AKA Rlip) in neuro-degenerative disorders, including Alzheimer's Disease (AD). However, the role of Rlip in Alzheimer's and other neurodegenerative diseases is not well understood. The purpose of the present study is to determine the role of Rlip in the brains of AD patients and control subjects. To achieve our goals, we used frozen tissues and formalin-fixed paraffin-embedded postmortem brains from AD patients of different Braak stages and age-matched control subjects. Our immunohistology and immunoblotting blotting analysis revealed that expression of Rlip protein gradually and significantly decreased (p = 0.0001) with AD progression, being lowest in Braak stage IV-V. Rlip was colocalized with Amyloid beta (A beta) and phosphorylated tau (p-Tau) as observed by IHC staining and co-immunoprecipitation studies. Lipid peroxidation (4-HNE generation) and H2O2 production were significantly higher (p = 0.004 and 0.0001 respectively) in AD patients compared to controls, and this was accompanied by lower ATP production in AD (p = 0.0009). Oxidative DNA damage was measured by 8-Hydroxyguanosine (8-OHdG) in tissue lysates by ELISA and COMET assay. AD 8-OHdG levels were significantly higher (p = 0.0001) compared to controls. COMET assay was performed in brain cells, isolated from frozen postmortem samples. The control samples showed minimal DNA in comets representing few DNA strand breaks (<20 %), (score-0-1). However, the AD group showed an average of 50 % to 65 % of DNA in comet tails (score-4-5) indicating numerous DNA strand breaks. The difference between the two groups was significant (p = 0.001), as analyzed by Open Comet by ImageJ. Elevated DNA damage was further examined by western blot analysis for phosphorylated histone variant H2AX (gamma H2AX). Induction of gamma H2AX was very significant (p < 0.0001) and confirmed the presence of double-strand breaks in DNA. Overall, our results indicate an important role for Rlip in maintaining neuronal health and homeostasis by suppressing cellular oxidative stress and DNA damage. Based on our find-ings, we cautiously conclude that Rlip is a promising therapeutic target for Alzheimer's disease.

Automated summary

This study investigates the role of RLIP76 in Alzheimer's Disease (AD) by analyzing brain tissues from AD patients and control subjects. The findings show a gradual decrease in the expression of RLIP76 protein with AD progression, and its co-localization with Amyloid beta and phosphorylated tau. AD patients exhibited higher levels of lipid peroxidation, H2O2 production, and oxidative DNA damage, as well as lower ATP production compared to controls. COMET assay revealed numerous DNA strand breaks in AD patients. These results indicate that RLIP76 plays an important role in maintaining neuronal health and homeostasis, and could be a promising therapeutic target for Alzheimer's disease.