Department of Cellular and Molecular Medicine, Kidney Research Centre, Faculty of Medicine, University of Ottawa, Ottawa, ON, Canada K1H 8M5.
PPAR Res. 2009;2009:706283. doi: 10.1155/2009/706283. Epub 2009 Mar 4.
The collecting duct (CD) expresses considerable amounts of PPARδ. While its role is unknown in the CD, in other renal cells it has been shown to regulate both growth and apoptosis. We thus hypothesized that PPARδ reduces apoptotic responses and stimulates cell growth in the mouse CD, and examined the effect of GW501516, a synthetic PPARδ ligand, on these responses in mouse IMCD-K2 cells. High doses of GW501516 decreased both DNA and protein synthesis in these cells by 80%, but had no overall effect on cell viability. Although anisomycin treatment resulted in an increase of caspase-3 levels of about 2.59-fold of control, GW501516 did not affect anisomycin-induced changes in active caspase-3 levels. These results show that a PPARδ ligand inhibits growth but does not affect anisomycin-apoptosis in a mouse IMCD cell line. This could have therapeutic implications for renal diseases associated with increased CD growth responses.
集合管(CD)表达相当数量的 PPARδ。虽然其在 CD 中的作用尚不清楚,但在其他肾脏细胞中,已经表明它可以调节生长和细胞凋亡。因此,我们假设 PPARδ 可减少小鼠 CD 中的细胞凋亡反应并刺激细胞生长,并研究了合成的 PPARδ 配体 GW501516 对这些反应的影响。高剂量的 GW501516 使这些细胞的 DNA 和蛋白质合成分别减少了 80%,但对细胞活力没有总体影响。尽管放线菌酮处理导致 caspase-3 水平增加约 2.59 倍,但 GW501516 不影响放线菌酮诱导的活性 caspase-3 水平的变化。这些结果表明,PPARδ 配体抑制生长,但不影响小鼠 IMCD 细胞系中放线菌酮诱导的细胞凋亡。这可能对与 CD 生长反应增加相关的肾脏疾病具有治疗意义。