Regulation of RSPO3-LGR4 Signaling: Emerging Role in Inflammation Revealed by Network Analysis

Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.

• Level A · Stronger Clinical Evidence
• Level B · Emerging clinical evidence with positive signals
• Level C · Early human research exploring benefits
• Level D · Scientific groundwork from lab and animal studies
• Emerging · Emerging topic under active research

Abstract (original English)

RSPO3, as a member of the R-spondin gene family, is a secreted molecule that enhances one of the fundamental biological pathways, the canonical Wnt signaling pathway. Once secreted from endothelial cells or macrophages, it typically binds to specific receptors from the LGR family. Additionally, LGR-independent activation of the Wnt cascade, driven by RSPOs, has also been described, mediated by heparan sulfate proteoglycans (HSPGs). LGR4 (GPR48) belongs to the G-protein-coupled receptor superfamily, subfamily B. It is widely recognized as an RSPO3-binding receptor and, thereafter, a Wnt signaling potentiator. Expression patterns of both RSPO3 and LGR4 have been found across various tissues. RSPO3 regulates stem cell maintenance in the intestine, in addition to its function in liver endothelial cells in terms of liver zonation or osteoblast differentiation. LGR4 has shown expression in hypothalamic neurons, regulating reproductive hormone secretion and control of food intake. Various studies reported the contribution of both RSPO3 and LGR4 to inflammatory cascades. Specifically, the RSPO3-LGR4 ligand-receptor interaction was shown to activate the NLRP3 inflammasome and β-catenin-NF-kB signaling cascade. Endothelial-derived RSPO3 exerts regenerative potential via the RSPO3-LGR4-ILK-AKT pathway, as presented in vitro model of inflammatory vascular injury. As a reaction to H.pylori

Evidence level

Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.

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