AUTHOR=Barrell William B. , Griffin John N. , Harvey Jessica-Lily , HipSci Consortium , Danovi Davide , Beales Philip , Grigoriadis Agamemnon E. , Liu Karen J. , Durbin Richard , Gaffney Daniel , Agu Chukwuma , Alderton Alex , Amatya Shrada , Danecek Petr , Denton Rachel , Goncalves Angela , Halai Reena , Harper Sarah , Kirton Chris , Knights Andrew , Kolb-Kokocinski Anja , Leha Andreas , McCarthy Shane , Memari Yasin , Patel Minal , Birney Ewan , Stegle Oliver , Paolo Casale Francesco , Clarke Laura , Harrison Peter , Kilpinen Helena , McCarthy Davis , Streeter Ian , Watt Fiona , Denovi Davide , Meleckyte Ruta , Moens Natalie , Ouwehand Willem , Vallier Ludovic , Lamond Angus , Bensaddek Dalila , Beales Philip TITLE=Induction of Neural Crest Stem Cells From Bardet–Biedl Syndrome Patient Derived hiPSCs JOURNAL=Frontiers in Molecular Neuroscience VOLUME=12 YEAR=2019 URL=https://www.frontiersin.org/journals/molecular-neuroscience/articles/10.3389/fnmol.2019.00139 DOI=10.3389/fnmol.2019.00139 ISSN=1662-5099 ABSTRACT=

Neural crest cells arise in the embryo from the neural plate border and migrate throughout the body, giving rise to many different tissue types such as bones and cartilage of the face, smooth muscles, neurons, and melanocytes. While studied extensively in animal models, neural crest development and disease have been poorly described in humans due to the challenges in accessing embryonic tissues. In recent years, patient-derived human induced pluripotent stem cells (hiPSCs) have become easier to generate, and several streamlined protocols have enabled robust differentiation of hiPSCs to the neural crest lineage. Thus, a unique opportunity is offered for modeling neurocristopathies using patient specific stem cell lines. In this work, we make use of hiPSCs derived from patients affected by the Bardet–Biedl Syndrome (BBS) ciliopathy. BBS patients often exhibit subclinical craniofacial dysmorphisms that are likely to be associated with the neural crest-derived facial skeleton. We focus on hiPSCs carrying variants in the BBS10 gene, which encodes a protein forming part of a chaperonin-like complex associated with the cilium. Here, we establish a pipeline for profiling hiPSCs during differentiation toward the neural crest stem cell fate. This can be used to characterize the differentiation properties of the neural crest-like cells. Two different BBS10 mutant lines showed a reduction in expression of the characteristic neural crest gene expression profile. Further analysis of both BBS10 mutant lines highlighted the inability of these mutant lines to differentiate toward a neural crest fate, which was also characterized by a decreased WNT and BMP response. Altogether, our study suggests a requirement for wild-type BBS10 in human neural crest development. In the long term, approaches such as the one we describe will allow direct comparison of disease-specific cell lines. This will provide valuable insights into the relationships between genetic background and heterogeneity in cellular models. The possibility of integrating laboratory data with clinical phenotypes will move us toward precision medicine approaches.