Li Xiaogang, Magenheimer Brenda S, Xia Sheng, Johnson Teri, Wallace Darren P, Calvet James P, Li Rong
Stowers Institute for Medical Research, 1000 East 50th Street, Kansas City, Missouri 64110, USA.
Nat Med. 2008 Aug;14(8):863-8. doi: 10.1038/nm1783. Epub 2008 Jun 15.
Autosomal dominant polycystic kidney disease (ADPKD) is caused by heterozygous mutations in either PKD1 or PKD2, genes that encode polycystin-1 and polycystin-2, respectively. We show here that tumor necrosis factor-alpha (TNF-alpha), an inflammatory cytokine present in the cystic fluid of humans with ADPKD, disrupts the localization of polycystin-2 to the plasma membrane and primary cilia through a scaffold protein, FIP2, which is induced by TNF-alpha. Treatment of mouse embryonic kidney organ cultures with TNF-alpha resulted in formation of cysts, and this effect was exacerbated in the Pkd2(+/-) kidneys. TNF-alpha also stimulated cyst formation in vivo in Pkd2(+/-) mice. In contrast, treatment of Pkd2(+/-) mice with the TNF-alpha inhibitor etanercept prevented cyst formation. These data reveal a pathway connecting TNF-alpha signaling, polycystins and cystogenesis, the activation of which may reduce functional polycystin-2 below a critical threshold, precipitating the ADPKD cellular phenotype.
常染色体显性多囊肾病(ADPKD)是由PKD1或PKD2基因的杂合突变引起的,这两个基因分别编码多囊蛋白-1和多囊蛋白-2。我们在此表明,肿瘤坏死因子-α(TNF-α)是一种存在于患有ADPKD的人类囊液中的炎性细胞因子,它通过一种由TNF-α诱导的支架蛋白FIP2破坏多囊蛋白-2在质膜和初级纤毛上的定位。用TNF-α处理小鼠胚胎肾器官培养物会导致囊肿形成,并且这种效应在Pkd2(+/-)肾脏中会加剧。TNF-α还会在Pkd2(+/-)小鼠体内刺激囊肿形成。相比之下,用TNF-α抑制剂依那西普治疗Pkd2(+/-)小鼠可防止囊肿形成。这些数据揭示了一条连接TNF-α信号传导、多囊蛋白和囊肿发生的途径,该途径的激活可能会使功能性多囊蛋白-2降至临界阈值以下,从而引发ADPKD细胞表型。