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Role of the Receptor for Advanced Glycation End Products (RAGE) and Its Ligands in Inflammatory Responses
Kaylen Cross1, Stefan W Vetter1, Yousuf Alam1
1Department of Pharmaceutical Sciences, North Dakota State University, Fargo, ND 58105, USA.
Abstract:
Since its discovery in 1992, the receptor for advanced glycation end products (RAGE) has emerged as a key receptor in many pathological conditions, especially in inflammatory conditions. RAGE is expressed by most, if not all, immune cells and can be activated by many ligands. One characteristic of RAGE is that its ligands are structurally very diverse and belong to different classes of molecules, making RAGE a promiscuous receptor. Many of RAGE ligands are damaged associated molecular patterns (DAMPs) that are released by cells under inflammatory conditions. Although RAGE has been at the center of a lot of research in the past three decades, a clear understanding of the mechanisms of RAGE activation by its ligands is still missing. In this review, we summarize the current knowledge of the role of RAGE and its ligands in inflammation.
Insights
The receptor for advanced glycation end products (RAGE) is crucial in inflammation, activated by diverse ligands like damage-associated molecular patterns (DAMPs). Further research is needed to clarify RAGE activation mechanisms.
Area of Science:
- Immunology
- Molecular Biology
- Pathology
Background:
- The receptor for advanced glycation end products (RAGE) was discovered in 1992.
- RAGE is implicated in numerous pathological conditions, particularly inflammatory diseases.
- It is expressed on most immune cells and activated by a wide array of structurally diverse ligands.
Purpose of the Study:
- To review the current understanding of RAGE's role in inflammation.
- To explore the diverse ligands that activate RAGE.
- To highlight the need for further research into RAGE activation mechanisms.
Main Methods:
- Literature review of research on RAGE and its ligands.
- Summary of known RAGE ligands, including damage-associated molecular patterns (DAMPs).
- Analysis of RAGE expression on immune cells.
Main Results:
- RAGE is a promiscuous receptor, binding to structurally diverse ligands.
- Many RAGE ligands are DAMPs released during inflammation.
- Despite extensive research, RAGE activation mechanisms remain unclear.
Conclusions:
- RAGE plays a significant role in inflammatory processes.
- The diverse nature of RAGE ligands contributes to its complex function.
- Elucidating RAGE activation mechanisms is essential for understanding inflammatory diseases.
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