Identification and characterization of early human photoreceptor states and cell-state-specific retinoblastoma-related features

This article has 10 evaluations Published on
Read the full article Related papers
This article on Sciety

Abstract

Human cone photoreceptors differ from rods and serve as the retinoblastoma cell-of-origin, yet the developmental basis for their distinct behaviors is poorly understood. Here, we used deep full-length single-cell RNA-sequencing (scRNA-seq) to distinguish post-mitotic cone and rod developmental states and identify cone-specific features that contribute to retinoblastomagenesis. The analyses revealed nascent, immediately post-mitotic cone- and rod precursor populations characterized by higher THRB or NRL regulon activities, immature and maturing cone and rod precursors with concurrent cone- and rod-related gene and regulon expression, and distinct early and late cone and rod maturation states distinguished by maturation-associated declines in RAX regulon activity. Cell-state-specific gene expression features inferred based on full-length scRNA-seq were consistent with past single nucleus 3’ RNA-seq analyses. Beyond the cell state characterizations, full-length scRNAseq revealed that both L/M cone and rod precursors co-expressedNRLandTHRBRNAs, yet they differentially expressed functionally antagonisticNRLandTHRBisoforms and prematurely terminatedTHRBtranscripts. Moreover, early L/M cone precursors exhibited successive expression of several lncRNAs along withMYCN, which composed the seventh most L/M-cone-specific regulon, andSYK, which was implicated in the cone precursors’ proliferative response toRB1loss. These findings reveal previously unresolved photoreceptor precursor states and suggest a role for early cone-precursor-intrinsicSYKexpression in retinoblastoma initiation.

Impact Statement

Features acquired by early post-mitotic retinal cells underlie the distinct behaviors of rods and the cone cells of origin of retinoblastoma tumors.

Related articles

Related articles are currently not available for this article.