Inflammation Is More Sensitive than Cell Proliferation in Response to Rapamycin Treatment in Polycystic Kidney Disease

被引:2
作者
Yang, Ming [1 ]
Lv, Jiayi [2 ]
Gong, Chanjuan [2 ]
Xue, Cheng [2 ]
Fu, Lili [2 ]
Chen, Shunjie [1 ]
Mei, Changlin [1 ,2 ]
机构
[1] Tongji Univ, Shanghai Peoples Hosp 4, Sch Med, Dept Nephrol, Shanghai, Peoples R China
[2] Naval Med Univ, Mil Med Univ 2, Shanghai Changzheng Hosp, Dept Nephrol,Affiliated Hosp 2, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
Rapamycin; Inflammation; Cell proliferation; Polycystic kidney disease; SIROLIMUS; PROGRESSION; MTOR; INHIBITION; ACTIVATION; PATHWAY; PATHOGENESIS; TOLVAPTAN; THERAPY; GROWTH;
D O I
10.1159/000535750
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Introduction: It has been reported that rapamycin inhibited inflammation in renal interstitial diseases. We therefore hypothesized that rapamycin could attenuate inflammation in polycystic kidney disease (PKD). Methods: Han:SPRD rats were treated with rapamycin by daily gavage from 4 weeks to 12 weeks of age at the dosage of 0.5 mg/kg/day (low dose) or 1 mg/kg/day (high dose). WT9-12 human PKD cells were treated with various concentrations of rapamycin. Results: Two-kidney/total body weight ratio and cystic index in Cy/+ kidneys were significantly reduced with the treatment of low-dose rapamycin and further reduced by the treatment with high-dose rapamycin. However, the renal function of Cy/+ rats was equally improved by the treatment with either low-dose or high-dose rapamycin. The renal cell proliferation was significantly decreased in Cy/+ kidneys with the treatment of low-dose rapamycin and was further decreased with the treatment of high-dose rapamycin as examined by Ki67 staining. The phosphorylation of S6K in cystic kidneys was decreased by low-dose rapamycin and further decreased by high-dose rapamycin. Both low-dose and high-dose rapamycin treatment decreased macrophage infiltration and the expression of complement factor B (CFB), monocyte chemoattractant protein-1 (MCP-1), and tumor necrosis factor-alpha (TNF-alpha) to a similar level. The expression of CFB, MCP-1, and TNF-alpha and phosphorylation of S6K were inhibited in WT9-12 cells treated with 10 nm rapamycin at 24 h and 48 h, respectively. Moreover, the phosphorylation of Akt was not increased by 1 nm and 10 nm of rapamycin and enhanced by 1 mu m rapamycin treatment. Interestingly, WT9-12 cell proliferation could be inhibited by 1 mu m rapamycin. Conclusion: Low dose of rapamycin could inhibit inflammation and protect renal function in PKD. Inflammation is more sensitive than cell proliferation in response to rapamycin treatment in PKD.
引用
收藏
页码:60 / 68
页数:9
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