Expression Patterns and Roles of Periostin During Kidney and Ureter Development

被引:26
作者
Sorocos, Katrina [1 ]
Kostoulias, Xenia [1 ]
Cullen-McEwen, Luise [1 ]
Hart, Adam H. [1 ]
Bertram, John F. [1 ]
Caruana, Georgina [1 ]
机构
[1] Monash Univ, Sch Biomed Sci, Dept Anat & Dev Biol, Melbourne, Vic, Australia
关键词
ureter; kidney; bone morphogenetic protein 4; myocytes; smooth muscle; fetal development; OSTEOBLAST-SPECIFIC FACTOR; IN-VITRO; GROWTH; CELLS; DIFFERENTIATION; MESENCHYME; INTEGRINS; PATHWAY; CLONING; CANCER;
D O I
10.1016/j.juro.2011.05.042
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Purpose: Periostin is a secreted extracellular matrix protein that is differentially expressed in the developing kidney. We analyzed the temporal-spatial expression of periostin in the developing kidney and ureter as well as its roles in ureter branching morphogenesis, nephrogenesis and ureter development. Materials and Methods: RNA in situ hybridization and immunofluorescence histochemistry were used to investigate the expression of periostin, alpha v integrin and alpha-smooth muscle actin during mouse renal and ureteral development. Metanephric explants were cultured in the presence of recombinant periostin, and ureteral branch points/tips and the glomerular number were quantified. Explants were also cultured in the presence of exogenous bone morphogenetic protein 4 and the effect on periostin mRNA levels was determined by quantitative real-time polymerase chain reaction. Results: Periostin expression was observed in the mesenchyme surrounding the kidney and ureter, renal stroma, metanephric mesenchyme, ureter epithelium and developing nephrons. At embryonic day 15.5 periostin and alpha v integrin, a common subunit of periostin receptors, were co-expressed in smooth muscle cells of the ureter, renal artery and intrarenal arteries. Bone morphogenetic protein 4 up-regulated periostin mRNA expression and exogenous periostin inhibited branching morphogenesis and glomerular number. Conclusions: Bone morphogenetic protein 4 which inhibits ureteral branching morphogenesis and promotes smooth muscle cell migration in the ureter up-regulated periostin mRNA expression in the developing kidney. Ureteral smooth muscle cells express periostin and alpha v integrin. Periostin inhibited ureteral branching morphogenesis and glomerular number. Together these results suggest that periostin and bone morphogenetic protein 4 may have a role in branching morphogenesis, nephrogenesis and possibly smooth muscle cell migration.
引用
收藏
页码:1537 / 1544
页数:8
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