| Literature DB >> 28720653 |
Manali Dimri1, Cassandra Bilogan1, Lain X Pierce1, Gregory Naegele1, Amit Vasanji2, Isabel Gibson1, Allyson McClendon1, Kevin Tae1, Takuya F Sakaguchi3,4.
Abstract
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 cdk5 regulatory subunit 1a (cdk5r1a), an essential activator of Cdk5. cdk5r1a 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.Entities:
Keywords: Actin dynamics; Biliary atresia; Biliary epithelial cells; Cdk5r1a; Intrahepatic biliary network
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Year: 2017 PMID: 28720653 PMCID: PMC5536925 DOI: 10.1242/dev.147397
Source DB: PubMed Journal: Development ISSN: 0950-1991 Impact factor: 6.868