Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8310177 | Clinica Chimica Acta | 2016 | 8 Pages |
Abstract
Apelin, an endogenous ligand of the G-protein-coupled receptor APJ, is expressed in a diverse number of organs. The apelin-APJ axis helps to control the processes of pathological and physiological fibrosis, including renal fibrosis, cardiac fibrosis, liver fibrosis and pulmonary fibrosis. However, the role of apelin-APJ in organ fibrosis remains controversial due to conflicting study results. The apelin-APJ axis is a detrimental mechanism which promotes liver fibrosis mainly via up-regulation the expression of collagen-II and platelet-derived growth factor receptor β (PDGFRβ). On the contrary, the apelin-APJ axis is beneficial for renal fibrosis, cardiac fibrosis and pulmonary fibrosis. The apelin-APJ axis alleviates renal fibrosis by restraining the expression of transforming growth factor-β1 (TGF-β1). In addition, the apelin-APJ axis attenuates cardiac fibrosis through multiple pathways. Furthermore, the apelin-APJ axis has beneficial effects on experimental bronchopulmonary dysplasia (BPD) and acute respiratory distress syndrome (ARDS) which suggest the apelin-APJ axis potentially alleviates pulmonary fibrosis. In this article, we review the controversies associated with apelin-APJ in organ fibrosis and introduce the drugs that target apelin-APJ. We conclude that future studies should place more emphasis on the relationship among apelin isoforms, APJ receptor subtypes and organ fibrosis. The apelin-APJ axis will be a potential therapeutic target and those drugs targeted for apelin-APJ may constitute a novel therapeutic strategy for renal fibrosis, cardiac fibrosis, liver fibrosis and pulmonary fibrosis.
Keywords
VSMCUUOSphK1AT-1PAI-1ECMeNOSTGF-β1angiotensin II type 1 receptorAngiotensin IIUnilateral ureteral obstructioncoronary artery diseasechronic kidney diseaseTransforming growth factor-β1EMTAng-IIVascular smooth muscle cellendothelial nitric oxide synthaseCADExtracellular matrixPlasminogen activator inhibitor-1CKDEpithelial–mesenchymal transition
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Authors
Shifang Huang, Linxi Chen, Liqun Lu, Lanfang Li,