Oxalate-induced crystalline kidney injury is a common form of crystal nephropathy.The accumulation of calcium oxalate(CaOx)crystal could lead to renal epithelium injury and inflammation.The underlying cellular events ...Oxalate-induced crystalline kidney injury is a common form of crystal nephropathy.The accumulation of calcium oxalate(CaOx)crystal could lead to renal epithelium injury and inflammation.The underlying cellular events in kidney after CaOx crystal formation are largely unknown.This study was aimed to gain a better understanding of mouse kidney function in the development of renal CaOx formation.The study utilized a mouse CaOx model to analyze the cellular response at 5 time points using single-cell RNA sequencing and investigate the interaction of different cells during renal CaOx crystal formation.Additionally,the study investigated the communication between these cells and macrophages,as well as the role of chemokines in recruiting infiltrating macrophages.RNA velocity analysis uncovered an alternative differentiation pathway for injured and S1 proximal tubule cells,which mainly communicate with macrophages through the SPP1-CD44 pair,along with the expression of proinflammatory factors and stone matrix genes during renal CaOx crystal formation.Furthermore,resident Fn1 macrophages were found to express chemokines,such as CCL2,which recruited infiltrating macrophages.The CCL2 secretion was mediated by the CD44-AKT pathway.Blocking CCL2 decreased the expression of injury markers in the kidney,including CLU,LCN2,and KIM-1,and inhibited CaOx crystal deposition.The study identified potential cell types and target genes involved in renal tubule injury in oxalate-related crystal nephropathy.The findings shed light on the cellular processes that contribute to the formation and damage caused by CaOx crystals within the kidney,which could lead to the development of potential cell types and target genes for treating this condition.展开更多
基金funded by the Science&Technology Department of Sichuan Province(2022YFS0304 and 2023YFS0029)the National Natural Science Foundation of China(82270799,81970602,and 82173251)+2 种基金the 1·3·5 Project of West China Hospital,Sichuan University(2023HXFH014)the Clinical Research Incubation Project of West China Hospital of Sichuan University(18HXFH012)ShangYao of West China Hospital of Sichuan University(19HXCX004).
文摘Oxalate-induced crystalline kidney injury is a common form of crystal nephropathy.The accumulation of calcium oxalate(CaOx)crystal could lead to renal epithelium injury and inflammation.The underlying cellular events in kidney after CaOx crystal formation are largely unknown.This study was aimed to gain a better understanding of mouse kidney function in the development of renal CaOx formation.The study utilized a mouse CaOx model to analyze the cellular response at 5 time points using single-cell RNA sequencing and investigate the interaction of different cells during renal CaOx crystal formation.Additionally,the study investigated the communication between these cells and macrophages,as well as the role of chemokines in recruiting infiltrating macrophages.RNA velocity analysis uncovered an alternative differentiation pathway for injured and S1 proximal tubule cells,which mainly communicate with macrophages through the SPP1-CD44 pair,along with the expression of proinflammatory factors and stone matrix genes during renal CaOx crystal formation.Furthermore,resident Fn1 macrophages were found to express chemokines,such as CCL2,which recruited infiltrating macrophages.The CCL2 secretion was mediated by the CD44-AKT pathway.Blocking CCL2 decreased the expression of injury markers in the kidney,including CLU,LCN2,and KIM-1,and inhibited CaOx crystal deposition.The study identified potential cell types and target genes involved in renal tubule injury in oxalate-related crystal nephropathy.The findings shed light on the cellular processes that contribute to the formation and damage caused by CaOx crystals within the kidney,which could lead to the development of potential cell types and target genes for treating this condition.
