4.7 Article

Dual Nature of RAGE in Host Reaction and Nurturing the Mother-Infant Bond

期刊

出版社

MDPI
DOI: 10.3390/ijms23042086

关键词

receptor for advanced glycation end-products (RAGE); oxytocin; blood-brain barrier; intestinal barrier; maternal bonding; social behavior

资金

  1. Kanazawa University SAKIGAKE project 2020
  2. Takeda Science Foundation
  3. Japan Society for Promotion of Sciences [21H02695, 21K09317, 20K07323, 18K06889]
  4. Grants-in-Aid for Scientific Research [21H02695, 21K09317, 18K06889, 20K07323] Funding Source: KAKEN

向作者/读者索取更多资源

Non-enzymatic glycation is an unavoidable biological reaction, leading to the formation of advanced glycation end-products (AGEs) that are detrimental to human health. Receptor for AGEs (RAGE) acts as a pattern-recognition receptor and plays a role in various pathological processes through intracellular signaling pathways. RAGE is present in all mammals but absent in other vertebrates. This review provides an overview of RAGE biology, its involvement in physiological and pathological processes, different isoforms of RAGE, and the importance of oxytocin transporters in maternal bonding and social behaviors.
Non-enzymatic glycation is an unavoidable reaction that occurs across biological taxa. The final products of this irreversible reaction are called advanced glycation end-products (AGEs). The endogenously formed AGEs are known to be bioactive and detrimental to human health. Additionally, exogenous food-derived AGEs are debated to contribute to the development of aging and various diseases. Receptor for AGEs (RAGE) is widely known to elicit biological reactions. The binding of RAGE to other ligands (e.g., high mobility group box 1, S100 proteins, lipopolysaccharides, and amyloid-beta) can result in pathological processes via the activation of intracellular RAGE signaling pathways, including inflammation, diabetes, aging, cancer growth, and metastasis. RAGE is now recognized as a pattern-recognition receptor. All mammals have RAGE homologs; however, other vertebrates, such as birds, amphibians, fish, and reptiles, do not have RAGE at the genomic level. This evidence from an evolutionary perspective allows us to understand why mammals require RAGE. In this review, we provide an overview of the scientific knowledge about the role of RAGE in physiological and pathological processes. In particular, we focus on (1) RAGE biology, (2) the role of RAGE in physiological and pathophysiological processes, (3) RAGE isoforms, including full-length membrane-bound RAGE (mRAGE), and the soluble forms of RAGE (sRAGE), which comprise endogenous secretory RAGE (esRAGE) and an ectodomain-shed form of RAGE, and (4) oxytocin transporters in the brain and intestine, which are important for maternal bonding and social behaviors.

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