miR-183/96/182 cluster is an important morphogenetic factor targeting PAX6 expression in differentiating human retinal organoids.
Lucie PeskovaDenisa JurcikovaTereza VanovaJan KrivanekMichaela CapandovaZuzana SramkovaJana SebestikovaMagdalena KolouskovaHana KotasovaLibor StreitTomas BartaPublished in: Stem cells (Dayton, Ohio) (2020)
MicroRNAs (miRNAs), a class of small, noncoding RNA molecules represent important regulators of gene expression. Recent reports have implicated their role in the cell specification process acting as "fine-tuners" to ensure the precise gene expression at the specific stage of cell differentiation. Here, we used retinal organoids differentiated from human pluripotent stem cells (hPSCs) as a model to closely investigate the role of a sensory organ-specific and evolutionary conserved miR-183/96/182 cluster. Using a miRNA tough decoy approach, we inhibited the miR-183/96/182 cluster in hPSCs. Inhibition of the miRNA cluster resulted in an increased expansion of neuroepithelium leading to abnormal "bulged" neural retina in organoids, associated with upregulation of neural-specific and retinal-specific genes. Importantly, we identified PAX6, a well-known essential gene in neuroectoderm specification, as a target of the miR-183/96/182 cluster members. Taken together, the miR-183/96/182 cluster not only represents an important regulator of PAX6 expression, but it also plays a crucial role in retinal tissue morphogenesis.
Keyphrases
- cell proliferation
- long non coding rna
- poor prognosis
- gene expression
- diabetic retinopathy
- pluripotent stem cells
- long noncoding rna
- optical coherence tomography
- induced pluripotent stem cells
- endothelial cells
- optic nerve
- genome wide
- dna methylation
- transcription factor
- emergency department
- stem cells
- magnetic resonance
- air pollution
- copy number
- bone marrow
- cancer therapy
- mesenchymal stem cells
- drug induced