Gombart Sean K, Houghtaling Scott, Ho Tzu-Hua, Beier David R
Center for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, WA 98101, USA.
Department of Pediatrics, Division of Genetic Medicine, University of Washington School of Medicine, Seattle, WA 98195, USA.
J Cell Sci. 2025 Oct 15;138(20). doi: 10.1242/jcs.264133. Epub 2025 Jul 31.
Autosomal dominant polycystic kidney disease (ADPKD) is a monogenic disorder caused by mutations in PKD1 or PKD2, encoding polycystin-1 and polycystin-2, respectively. These polycystins form a cilia-localized complex that, when mutated, fails to inhibit an uncharacterized cilia-dependent cyst activation (CDCA) signal. This leads to progressive bilateral cyst growth and ultimately compromised renal function. Previous in vitro and in vivo studies from our group have demonstrated that Hedgehog (Hh) signaling inhibition reduces renal cystic severity in PKD models. To further investigate, we inactivated several Hh pathway components (Gli1, Gli2, Gli3 and Smo) in a Pkd1 hypomorphic mouse model through conditional deletion by tamoxifen-induced Cre-Lox recombination. We assessed cystic severity using kidney weight assessment and a microcomputed tomography (micro-CT)-based 3D imaging assay. Contrary to expectations, inactivation of Gli1 and Smo significantly increased cystogenesis. These findings suggest that Hh signaling does not mediate the CDCA signal.
常染色体显性多囊肾病(ADPKD)是一种单基因疾病,由PKD1或PKD2突变引起,分别编码多囊蛋白-1和多囊蛋白-2。这些多囊蛋白形成一种定位于纤毛的复合物,当发生突变时,该复合物无法抑制一种未明确的依赖纤毛的囊肿激活(CDCA)信号。这会导致双侧囊肿进行性生长,并最终损害肾功能。我们团队之前的体外和体内研究表明,刺猬信号通路(Hh)抑制可降低多囊肾病模型中肾囊肿的严重程度。为了进一步研究,我们通过他莫昔芬诱导的Cre-Lox重组条件性缺失,在Pkd1低表达小鼠模型中使几种Hh信号通路成分(Gli1、Gli2、Gli3和Smo)失活。我们使用肾脏重量评估和基于微计算机断层扫描(micro-CT)的三维成像分析来评估囊肿严重程度。与预期相反,Gli1和Smo的失活显著增加了囊肿形成。这些发现表明,Hh信号通路并不介导CDCA信号。