Receptor for the Advanced Glycation End Products ( RAGE ) Pathway in Adipose Tissue Metabolism.
Klaudia GutowskaKrzysztof CzajkowskiAlina Ewa KuryłowiczPublished in: International journal of molecular sciences (2023)
Advanced glycation end products (AGEs) are mediators in the process of cellular dysfunction in response to hyperglycemia. Numerous data indicate that the accumulation of AGEs in the extracellular matrix plays a key role in the development of obesity-related adipose tissue dysfunction. Through binding of their membrane receptor ( RAGE ), AGEs affect numerous intracellular pathways and impair adipocyte differentiation, metabolism, and secretory activity. Therefore, inhibiting the production and accumulation of AGEs, as well as interfering with the metabolic pathways they activate, may be a promising therapeutic strategy for restoring normal adipose tissue function and, thus, combating obesity-related comorbidities. This narrative review summarizes data on the involvement of the RAGE pathway in adipose tissue dysfunction in obesity and the development of its metabolic complications. The paper begins with a brief review of AGE synthesis and the RAGE signaling pathway. The effect of the RAGE pathway on adipose tissue development and activity is then presented. Next, data from animal and human studies on the involvement of the RAGE pathway in obesity, diabetes, and cardiovascular diseases are summarized. Finally, therapeutic perspectives based on interference with the RAGE pathway are discussed.
Keyphrases
- adipose tissue
- insulin resistance
- type diabetes
- high fat diet
- metabolic syndrome
- high fat diet induced
- signaling pathway
- weight loss
- extracellular matrix
- cardiovascular disease
- electronic health record
- weight gain
- big data
- endothelial cells
- glycemic control
- body mass index
- cell proliferation
- coronary artery disease
- data analysis
- induced apoptosis
- induced pluripotent stem cells