Quantum Dots‐caused Retinal Degeneration in Zebrafish Regulated by Ferroptosis and Mitophagy in Retinal Pigment Epithelial Cells through Inhibiting Spliceosome

Abstract: Quantum dots (QDs) are widely used, but their health impact on the visual system is little known. This study aims to elucidate the effects and mechanisms of typical metallic QDs on retinas using zebrafish. Comprehensive histology, imaging, and bulk RNA sequencing reveal that InP/ZnS QDs cause retinal degeneration. Furthermore, single‐cell RNA‐seq reveals a reduction in the number of retinal pigment epithelial cells (RPE) and short‐wave cone UV photoreceptor cells (PR (UV)), accompanied by an increase in middle‐ and long‐wave cone red, green, and blue photoreceptor cells [PR (RGB)]. Mechanistically, after endocytosis by RPE, InP/ZnS QDs inhibit the expression of splicing factor prpf8, resulting in gpx4b mRNA unsplicing, which finally decrease glutathione and induce ferroptosis and mitophagy. The decrease of RPE fails to engulf the damaged outer segments of PR, possibly promoting the differentiation of PR (UV) to PR (RGB). Knockout prpf8 or gpx4b with CRISPR/Cas9 system, the retinal damage is also observed. Whereas, overexpression of prpf8 or gpx4b, or supplement of glutathione can rescue the retinal degenerative damage caused by InP/ZnS QDs. In conclusion, this study illustrates the potential health risks of InP/ZnS QDs on eye development and provides valuable insights into the underlying mechanisms of InP/ZnS QDs‐caused retinal degeneration.

Angaben zum Objekt

• Standort: Deutsche Nationalbibliothek Frankfurt am Main
• Umfang: Online-Ressource
• Sprache: Englisch

Verweise und Beziehungen

• Erschienen in: Quantum Dots‐caused Retinal Degeneration in Zebrafish Regulated by Ferroptosis and Mitophagy in Retinal Pigment Epithelial Cells through Inhibiting Spliceosome ; day:17 ; month:10 ; year:2024 ; extent:19 ; Advanced science ; (17.10.2024) (gesamt 19)

Beteiligte, Orts- und Zeitangaben

• Urheber: Zheng, Naying ; Liao, Tingting ; Zhang, Chuchu ; Zhang, Zheyang ; Yan, Sen ; Xi, Xiaohan ; Ruan, Fengkai ; Yang, Chunyan ; Zhao, Qingliang ; Deng, Wenbo ; Huang, Jialiang ; Huang, Zi‐Tao ; Chen, Zhi‐Feng ; Wang, Xiang ; Qu, Qingming ; Zuo, Zhenghong ; He, Chengyong

Weitere Informationen

• DOI: 10.1002/advs.202406343
• URN: urn:nbn:de:101:1-2410181445364.516146279748
• Rechteinformation: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
• Letzte Aktualisierung: 15.08.2025, 07:22 MESZ