Transcriptome-Wide Analysis Reveals a Role for Extracellular Matrix and Integrin Receptor Genes in Otic Neurosensory Differentiation from Human iPSCs

• Published in: International journal of molecular sciences Vol. 22; no. 19; p. 10849
• Main Authors: Johnson Chacko, Lejo, Lahlou, Hanae, Steinacher, Claudia, Assou, Said, Messat, Yassine, Dudás, József, Edge, Albert, Crespo, Berta, Crosier, Moira, Sergi, Consolato, Schrott-Fischer, Anneliese, Zine, Azel
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 01.10.2021; MDPI
• Subjects: Cell culture; Cell differentiation; Cell fate; Cell lineage; Collagen; Differentiation; Ear; Extracellular matrix; Fetuses; GATA-3 protein; Gene expression; gene expression analysis; Genes; human fetal inner ear; human induced pluripotent stem cells; Immunocytochemistry; Inhibitory postsynaptic potentials; Inner ear; integrins; Life Sciences; Morphogenesis; otic sensory progenitors; Pluripotency; SIX gene family; Stem cells; Transcription factors; Transcriptomes
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms221910849

We analyzed transcriptomic data from otic sensory cells differentiated from human induced pluripotent stem cells (hiPSCs) by a previously described method to gain new insights into the early human otic neurosensory lineage. We identified genes and biological networks not previously described to occur in the human otic sensory developmental cell lineage. These analyses identified and ranked genes known to be part of the otic sensory lineage program (SIX1, EYA1, GATA3, etc.), in addition to a number of novel genes encoding extracellular matrix (ECM) (COL3A1, COL5A2, DCN, etc.) and integrin (ITG) receptors (ITGAV, ITGA4, ITGA) for ECM molecules. The results were confirmed by quantitative PCR analysis of a comprehensive panel of genes differentially expressed during the time course of hiPSC differentiation in vitro. Immunocytochemistry validated results for select otic and ECM/ITG gene markers in the in vivo human fetal inner ear. Our screen shows ECM and ITG gene expression changes coincident with hiPSC differentiation towards human otic neurosensory cells. Our findings suggest a critical role of ECM-ITG interactions with otic neurosensory lineage genes in early neurosensory development and cell fate determination in the human fetal inner ear.