Section of Nephrology, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT 06520, USA.
J Am Soc Nephrol. 2011 Oct;22(10):1809-14. doi: 10.1681/ASN.2011010084. Epub 2011 Sep 15.
Polycystic kidney disease (PKD) exhibits an inflammatory component, but the contribution of inflammation to cyst progression is unknown. Macrophages promote the proliferation of tubular cells following ischemic injury, suggesting that they may have a role in cystogenesis. Furthermore, cultured Pkd1-deficient cells express the macrophage chemoattractants Mcp1 and Cxcl16 and stimulate macrophage migration. Here, in orthologous models of both PKD1 and PKD2, abnormally large numbers of alternatively activated macrophages surrounded the cysts. To determine whether pericystic macrophages contribute to the proliferation of cyst-lining cells, we depleted phagocytic cells from Pkd1(fl/fl);Pkhd1-Cre mice by treating with liposomal clodronate from postnatal day 10 until day 24. Compared with vehicle-treated controls, macrophage-depleted mice had a significantly lower cystic index, reduced proliferation of cyst-lining cells, better-preserved renal parenchyma, and improved renal function. In conclusion, these data suggest that macrophages home to cystic areas and contribute to cyst growth. Interruption of these homing and proliferative signals could have therapeutic potential for PKD.
多囊肾病(PKD)表现出炎症成分,但炎症对囊肿进展的贡献尚不清楚。巨噬细胞在缺血性损伤后促进肾小管细胞的增殖,表明它们可能在囊肿发生中起作用。此外,培养的 Pkd1 缺陷细胞表达巨噬细胞趋化因子 Mcp1 和 Cxcl16 并刺激巨噬细胞迁移。在这里,在 PKD1 和 PKD2 的同源模型中,大量的交替激活的巨噬细胞包围着囊肿。为了确定囊周巨噬细胞是否有助于囊衬细胞的增殖,我们从出生后第 10 天至第 24 天用脂质体氯膦酸盐处理 Pkd1(fl/fl);Pkhd1-Cre 小鼠以耗尽吞噬细胞。与载体处理的对照组相比,巨噬细胞耗竭小鼠的囊泡指数明显降低,囊衬细胞增殖减少,肾实质保存更好,肾功能改善。总之,这些数据表明巨噬细胞归巢到囊性区域并促进囊肿生长。阻断这些归巢和增殖信号可能对 PKD 具有治疗潜力。