Generation of a Double Reporter mES Cell Line to Simultaneously Trace the Generation of Retinal Progenitors and Photoreceptors
- Oleksandr Zabiegalov 1, Adeline Berger 2, Dhryata Kamdar 3,4, Kabirou Adamou 5, Chuanxi Tian 1, Martial Mbefo 1, Mathieu Quinodoz 3,4, Florian Udry 1, Carlo Rivolta 3,4, Corinne Kostic 5, Yvan Arsenijevic 1
- Oleksandr Zabiegalov 1, Adeline Berger 2, Dhryata Kamdar 3,4
- 1Unit of Retinal Degeneration and Regeneration, Department of Ophthalmology, University of Lausanne, 1004 Lausanne, Switzerland.
- 2Unit of Epigenetics of Ocular Diseases, Department of Ophthalmology, University of Lausanne, 1004 Lausanne, Switzerland.
- 3Ophthalmic Genetics Group, Institute of Molecular and Clinical Ophthalmology, 4031 Basel, Switzerland.
- 4Department of Ophthalmology, University of Basel, 4031 Basel, Switzerland.
- 5Group for Retinal Disorders Research, Department of Ophthalmology, University of Lausanne, 1004 Lausanne, Switzerland.
- 0Unit of Retinal Degeneration and Regeneration, Department of Ophthalmology, University of Lausanne, 1004 Lausanne, Switzerland.
Related Experiment Videos
Contact us if these videos are not relevant.
Contact us if these videos are not relevant.
View abstract on PubMed
Summary
This summary is machine-generated.Researchers developed a new dual-reporter stem cell line to study retinal development and test therapies. This tool aids in isolating retinal progenitors and photoreceptors for faster research and drug development.
Area Of Science
- Stem cell biology
- Developmental biology
- Ophthalmology
Background
- Three-dimensional retinal organoids are crucial for studying eye development and disease.
- Existing methods lack efficient reporter stem cell lines for in vitro retinal research.
- Pure progenitor and photoreceptor precursor populations are needed for therapeutic development.
Purpose Of The Study
- To generate a dual-reporter mouse embryonic stem cell line for visualizing and isolating retinal progenitors and photoreceptors.
- To validate the utility of this reporter line in retinal organoid settings.
- To enable rapid in vitro investigation of retinal biology and therapeutic testing.
Main Methods
- Generation of a dual-reporter mouse embryonic stem cell line (Crx-GFP;Rax-mCherry).
- Isolation of mCherry-positive cells from day 4 retinal organoids.
- Proliferation assays, transcriptomic, and proteomic profiling of isolated cells.
Main Results
- The Crx-GFP;Rax-mCherry cell line successfully visualizes and isolates retinal progenitors and photoreceptors.
- Transcriptomic and proteomic analyses confirmed early retinal progenitor identity.
- The timing of key transcription factor expression aligns with natural mouse retinogenesis.
Conclusions
- The novel dual-reporter stem cell line facilitates efficient study of retinal development and disease.
- This tool accelerates research and therapeutic development compared to human induced pluripotent stem cells.
- The Crx-GFP;Rax-mCherry line is valuable for investigating biological questions and testing therapeutics in retinal organoids.
Related Experiment Videos
Contact us if these videos are not relevant.
Contact us if these videos are not relevant.

