<scp>DJ</scp> ‐1 ( <scp>PARK7</scp> ) as a Redox‐Responsive Integrator of Pancreatic, Hepatic, and Adipose Crosstalk in Glucose Homeostasis
DJ-1 (PARK7), originally characterized in Parkinson's disease, is increasingly recognized as a redox-sensitive regulator of systemic metabolism. Acting through oxidation-dependent modulation of Cys106, DJ-1 integrates cellular redox cues with mitochondrial function, insulin signaling, and stress adaptation pathways. In pancreatic β-cells, it preserves stimulus secretion coupling by stabilizing mitochondrial ATP production. In liver and adipose tissue, DJ-1 maintains insulin responsive signaling and metabolic flexibility through PTEN-PI3K-Akt and antioxidant networks. Loss or over-oxidation of DJ-1 disrupts interorgan glucose coordination, linking chronic redox imbalance to dysglycemia. This review positions DJ-1 as a metabolic sentinel translating oxidative inputs into integrated glucose regulatory outputs.
Authors
- Sarvesh Sabarathinam (ORCID: https://orcid.org/0000-0002-0792-392X)
- Navodi Sandamini Jayathilaka
- Jayasingha Mudiyanselage Pavithra Sewwandi Jayasingha
- Mallika Arachchige Hasantha Madushan
Institutions
- University of Sri Jayewardenepura (LK)
- Saveetha University (IN)
Publication Details
- Journal
- Comprehensive physiology
- Published
- 2026-03-15
- DOI
- https://doi.org/10.1002/cph4.70123
- Primary Topic
- Parkinson's Disease Mechanisms and Treatments
- Type
- article
- Field-Weighted Citation Impact
- 0.00