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RAGE: the beneficial and deleterious effects by diverse mechanisms of actions
Sun-Ho Han1, Yoon Hee Kim, Inhee Mook-Jung
1Department of Biochemistry and Biomedical Sciences, Seoul National University, College of Medicine, Seoul, Korea.
Abstract:
Receptor for advanced glycation endproducts (RAGE) is a transmembrane protein that belongs to the immunoglobulin superfamily. RAGE is expressed ubiquitously-high in lung and moderate to low in a wide range of cells-in a tightly regulated manner at various stages of development. RAGE is a pattern recognition receptor that binds to multiple ligands, including amphoterin, members of the S100/calgranulin family, the integrin Mac-1, and amyloid β-peptide (Aβ). RAGE-ligand engagement effects the activation of diverse cascades that initiate and stimulate chronic stress pathways and repair, depending on the ligand, environment, and developmental stage. Further, RAGE-ligand interaction and the consequent upregulation of RAGE through a positive feedback loop are often associated with various diseases, including vascular disease, diabetes, cancer, and neurodegenerative disease. It is unknown how RAGE mediates these events, but such phenomena appear to be linked to the inflammatory response. In this review, we summarize the findings on RAGE from published reports and ongoing studies. Also, the implication of RAGE in Alzheimer disease, the most common neurodegenerative disease in the elderly population, will be discussed, with a focus on Aβ-RAGE interactions with regard to signaling pathways and their impact on cellular activity.
Insights
The Receptor for Advanced Glycation Endproducts (RAGE) is a key protein involved in cellular stress and repair. Its interaction with ligands like amyloid-beta is implicated in neurodegenerative diseases such as Alzheimer's.
Area of Science:
- Cellular Biology
- Immunology
- Neuroscience
Background:
- Receptor for Advanced Glycation Endproducts (RAGE) is an immunoglobulin superfamily transmembrane protein.
- RAGE is ubiquitously expressed and acts as a pattern recognition receptor binding multiple ligands.
- RAGE-ligand interactions trigger diverse signaling cascades involved in stress and repair.
Purpose of the Study:
- To review current findings on RAGE.
- To discuss the role of RAGE in Alzheimer's disease (AD).
- To focus on amyloid-beta (Aβ)-RAGE interactions in AD pathogenesis.
Main Methods:
- Literature review of published reports and ongoing studies on RAGE.
- Analysis of RAGE-ligand interactions, particularly Aβ-RAGE.
- Examination of downstream signaling pathways and cellular effects.
Main Results:
- RAGE-ligand engagement activates chronic stress and repair pathways.
- Positive feedback loops in RAGE-ligand interaction are linked to diseases like diabetes, cancer, and neurodegeneration.
- Aβ-RAGE interactions are central to RAGE's implication in Alzheimer's disease.
Conclusions:
- RAGE plays a significant role in various diseases, potentially through inflammatory responses.
- Understanding Aβ-RAGE signaling is crucial for elucidating Alzheimer's disease mechanisms.
- Further research is needed to fully understand RAGE-mediated events and therapeutic potential.
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