Dicer is essential for proper maturation, composition, and function in the postnatal retina

The impact of Dicer/miRNAs during postnatal retinogenesis is unknown. This study aimed to deplete Dicer in postnatal retinal progenitor/precursor cells (RPCs/PCs) and to evaluate the structure and function of the adult Dicer-cKO retina using optical coherence tomography (OCT), electroretinography (ERG), and histology. We found impaired rod function, a significantly reduced number of rod bipolar cells and their associated functions, a decreased Müller glia population, and an increased population of HuC/D + Pax6/+ amacrine cells in the adult Dicer-cKO retina. Transcriptional analyses conducted in one-week-old mice showed early alterations in mRNA and miRNA levels. Single-cell RNA sequencing and initial histological analysis in young mice revealed a delay in differentiation/incomplete maturation, as indicated by an enlarged progenitor/precursor population at young ages that persists into adulthood. This suggests that Dicer/miRNAs in late RPC/PCs are essential for the proper formation and maturation of late RPC progenies and may also play a role in regulating cell state.

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Journal
iScience
Published
2025-10-18
DOI
https://doi.org/10.1016/j.isci.2025.113794
Primary Topic
Retinopathy of Prematurity Studies
Type
article
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article

Dicer is essential for proper maturation, composition, and function in the postnatal retina

S. Chen, Julia Jager, Konstantin Hahne, Khulan Batsuuri et al.
iScience
Retinopathy of Prematurity Studies
article

Dicer is essential for proper maturation, composition, and function in the postnatal retina

S. Chen, Julia Jager, Konstantin Hahne, Khulan Batsuuri, Brian S. Clark, Mônica Viégas Andrade, Stefanie G. Wohl, Suresh Viswanathan, Seoyoung Kang, Alireza Khodadadi‐Jamayran, Chaitra Sreenivasaiah, Daniel Larbi, Mariângela Carneiro, Eik Bruns
article en

Abstract

The impact of Dicer/miRNAs during postnatal retinogenesis is unknown. This study aimed to deplete Dicer in postnatal retinal progenitor/precursor cells (RPCs/PCs) and to evaluate the structure and function of the adult Dicer-cKO retina using optical coherence tomography (OCT), electroretinography (ERG), and histology. We found impaired rod function, a significantly reduced number of rod bipolar cells and their associated functions, a decreased Müller glia population, and an increased population of HuC/D + Pax6/+ amacrine cells in the adult Dicer-cKO retina. Transcriptional analyses conducted in one-week-old mice showed early alterations in mRNA and miRNA levels. Single-cell RNA sequencing and initial histological analysis in young mice revealed a delay in differentiation/incomplete maturation, as indicated by an enlarged progenitor/precursor population at young ages that persists into adulthood. This suggests that Dicer/miRNAs in late RPC/PCs are essential for the proper formation and maturation of late RPC progenies and may also play a role in regulating cell state.

iScienceVol. 28(11)
Washington University in St. Louis (US), Office of Science (US), Indiana University Bloomington (US), New York University (US), SUNY College of Optometry (US)
Openalex Percentile: Top 56%
Retinopathy of Prematurity Studies
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