Dimri Manali, Bilogan Cassandra, Pierce Lain X, Naegele Gregory, Vasanji Amit, Gibson Isabel, McClendon Allyson, Tae Kevin, Sakaguchi Takuya F
Department of Stem Cell Biology and Regenerative Medicine, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195, USA.
ImageIQ Inc., Cleveland, OH 44195, USA.
Development. 2017 Jul 15;144(14):2595-2605. doi: 10.1242/dev.147397.
The intrahepatic biliary network is a highly branched three-dimensional network lined by biliary epithelial cells, but how its branching patterns are precisely established is not clear. We designed a new computer-based algorithm that quantitatively computes the structural differences of the three-dimensional networks. Utilizing the algorithm, we showed that inhibition of Cyclin-dependent kinase 5 (Cdk5) led to reduced branching in the intrahepatic biliary network in zebrafish. Further, we identified a previously unappreciated downstream kinase cascade regulated by Cdk5. Pharmacological manipulations of this downstream kinase cascade produced a crowded branching defect in the intrahepatic biliary network and influenced actin dynamics in biliary epithelial cells. We generated larvae carrying a mutation in (), an essential activator of Cdk5. mutant larvae show similar branching defects as those observed in Cdk5 inhibitor-treated larvae. A small-molecule compound that interferes with the downstream kinase cascade rescued the mutant phenotype. These results provide new insights into branching morphogenesis of the intrahepatic biliary network.
肝内胆管网络是一个由胆管上皮细胞排列的高度分支的三维网络,但尚不清楚其分支模式是如何精确建立的。我们设计了一种新的基于计算机的算法,用于定量计算三维网络的结构差异。利用该算法,我们发现抑制细胞周期蛋白依赖性激酶5(Cdk5)会导致斑马鱼肝内胆管网络分支减少。此外,我们确定了一个以前未被认识的受Cdk5调节的下游激酶级联反应。对该下游激酶级联反应进行药理学操作会在肝内胆管网络中产生拥挤的分支缺陷,并影响胆管上皮细胞中的肌动蛋白动力学。我们生成了携带Cdk5必需激活剂()突变的幼虫。突变幼虫表现出与Cdk5抑制剂处理幼虫中观察到的类似分支缺陷。一种干扰下游激酶级联反应的小分子化合物挽救了突变表型。这些结果为肝内胆管网络的分支形态发生提供了新的见解。