Cancer Research Institute, University of South China, Hengyang, Hunan, 421001, China.
Exp Cell Res. 2011 Jan 15;317(2):173-87. doi: 10.1016/j.yexcr.2010.09.012. Epub 2010 Sep 25.
Mutations in the PKHD1 gene result in autosomal recessive polycystic kidney disease (ARPKD) in humans. To determine the molecular mechanism of the cystogenesis in ARPKD, we recently generated a mouse model for ARPKD that carries a targeted mutation in the mouse orthologue of human PKHD1. The homozygous mutant mice display hepatorenal cysts whose phenotypes are similar to those of human ARPKD patients. By littermates of this mouse, we developed two immortalized renal collecting duct cell lines with Pkhd1 and two without. Under nonpermissive culture conditions, the Pkhd1(-/-) renal cells displayed aberrant cell-cell contacts and tubulomorphogenesis. The Pkhd1(-/-) cells also showed significantly reduced cell proliferation and elevated apoptosis. To validate this finding in vivo, we examined proliferation and apoptosis in the kidneys of Pkhd1(-/-) mice and their wildtype littermates. Using proliferation (PCNA and Histone-3) and apoptosis (TUNEL and caspase-3) markers, similar results were obtained in the Pkhd1(-/-) kidney tissues as in the cells. To identify the molecular basis of these findings, we analyzed the effect of Pkhd1 loss on multiple putative signaling regulators. We demonstrated that the loss of Pkhd1 disrupts multiple major phosphorylations of focal adhesion kinase (FAK), and these disruptions either inhibit the Ras/C-Raf pathways to suppress MEK/ERK activity and ultimately reduce cell proliferation, or suppress PDK1/AKT to upregulate Bax/caspase-9/caspase-3 and promote apoptosis. Our findings indicate that apoptosis may be a major player in the cyst formation in ARPKD, which may lead to new therapeutic strategies for human ARPKD.
PKHD1 基因突变导致人类常染色体隐性多囊肾病 (ARPKD)。为了确定 ARPKD 囊肿形成的分子机制,我们最近生成了一种携带人类 PKHD1 同源物靶向突变的 ARPKD 小鼠模型。纯合突变小鼠表现出肝肾功能囊肿,其表型与人类 ARPKD 患者相似。通过这些小鼠的同窝仔,我们开发了两种具有 Pkhd1 和两种没有 Pkhd1 的永生化肾集合管细胞系。在非许可培养条件下,Pkhd1(-/-)肾细胞显示出异常的细胞-细胞接触和管形成。Pkhd1(-/-)细胞还显示出显著降低的细胞增殖和升高的细胞凋亡。为了在体内验证这一发现,我们检查了 Pkhd1(-/-)小鼠及其野生型同窝仔肾脏中的增殖和凋亡。使用增殖(PCNA 和组蛋白-3)和凋亡(TUNEL 和 caspase-3)标志物,在 Pkhd1(-/-)肾脏组织中获得了与细胞中相似的结果。为了确定这些发现的分子基础,我们分析了 Pkhd1 缺失对多个假定信号调节剂的影响。我们证明 Pkhd1 的缺失破坏了粘着斑激酶 (FAK) 的多个主要磷酸化,这些破坏要么抑制 Ras/C-Raf 途径以抑制 MEK/ERK 活性并最终减少细胞增殖,要么抑制 PDK1/AKT 以上调 Bax/caspase-9/caspase-3 并促进细胞凋亡。我们的研究结果表明,细胞凋亡可能是 ARPKD 囊肿形成的主要因素,这可能为人类 ARPKD 带来新的治疗策略。