Randall's plaque and calcium oxalate stone formation: role for immunity and inflammation.
Saeed R KhanBenjamin K CanalesPaul R Dominguez-GutierrezPublished in: Nature reviews. Nephrology (2021)
Idiopathic calcium oxalate (CaOx) stones often develop attached to Randall's plaque present on kidney papillary surfaces. Similar to the plaques formed during vascular calcification, Randall's plaques consist of calcium phosphate crystals mixed with an organic matrix that is rich in proteins, such as inter-α-trypsin inhibitor, as well as lipids, and includes membrane-bound vesicles or exosomes, collagen fibres and other components of the extracellular matrix. Kidney tissue surrounding Randall's plaques is associated with the presence of classically activated, pro-inflammatory macrophages (also termed M1) and downregulation of alternatively activated, anti-inflammatory macrophages (also termed M2). In animal models, crystal deposition in the kidneys has been associated with the production of reactive oxygen species, inflammasome activation and increased expression of molecules implicated in the inflammatory cascade, including osteopontin, matrix Gla protein and fetuin A (also known as α2-HS-glycoprotein). Many of these molecules, including osteopontin and matrix Gla protein, are well known inhibitors of vascular calcification. We propose that conditions of urine supersaturation promote kidney damage by inducing the production of reactive oxygen species and oxidative stress, and that the ensuing inflammatory immune response promotes Randall's plaque initiation and calcium stone formation.
Keyphrases
- oxidative stress
- reactive oxygen species
- extracellular matrix
- immune response
- coronary artery disease
- anti inflammatory
- diabetic rats
- ischemia reperfusion injury
- chronic kidney disease
- binding protein
- dna damage
- poor prognosis
- induced apoptosis
- stem cells
- mesenchymal stem cells
- protein protein
- amino acid
- toll like receptor
- inflammatory response
- room temperature
- cystic fibrosis
- solid state
- dendritic cells
- staphylococcus aureus
- heat shock protein
- clear cell