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Updated: Jan 30, 2026

Isolation and Culture of Primary Retinal Müller Cells from Sprague-Dawley (SD) Rats
Published on: June 17, 2025
Characterization of the novel spontaneously immortalized rat Müller cell line SIRMu-1
Thaksaon Kittipassorn1, Cameron D Haydinger1, John P M Wood2
1School of Biological Sciences, Molecular Life Sciences Building, University of Adelaide, Adelaide, SA, 5005, Australia.
Abstract:
Müller cells (MCs) play a crucial role in the retina, and cultured MC lines are an important tool with which to study MC function. Transformed MC lines have been widely used; however, the transformation process can also lead to unwanted changes compared to the primary cells from which they were derived. To provide an alternative experimental tool, a novel monoclonal spontaneously immortalized rat Müller cell line, SIRMu-1, was derived from primary rat MCs and characterized. Immunofluorescence, western blotting and RNA sequencing demonstrate that the SIRMu-1 cell line retains similar characteristics to cultured primary MCs in terms of expression of the MC markers cellular retinaldehyde-binding protein, glutamine synthetase, S100, vimentin and glial fibrillary acidic protein at both the mRNA and protein levels. Both the cellular morphology and overall transcriptome of the SIRMu-1 cells are more similar to primary rat MCs than the commonly used rMC-1 cells, a well-described, transformed rat MC line. Furthermore, SIRMu-1 cells proliferate rapidly, have an effectively indefinite life span and a high transfection efficiency. The expression of Y chromosome specific genes confirmed that the SIRMu-1 cells are derived from male MCs. Thus, the SIRMu-1 cell line represents a valuable experimental tool to study roles of MCs in both physiological and pathological states.
Insights
A new spontaneously immortalized rat Müller cell line, SIRMu-1, offers a valuable research tool. It closely resembles primary Müller cells, retaining key markers and transcriptome profiles for studying retinal physiology and disease.
Area of Science:
- Ophthalmology
- Cell Biology
- Neuroscience
Background:
- Müller cells (MCs) are vital for retinal function.
- Cultured MC lines are essential research tools.
- Transformed MC lines may exhibit altered characteristics compared to primary cells.
Purpose of the Study:
- To derive and characterize a novel spontaneously immortalized rat Müller cell line, SIRMu-1.
- To provide an alternative experimental tool that better reflects primary MC characteristics.
- To assess the suitability of SIRMu-1 for studying MCs in physiological and pathological conditions.
Main Methods:
- Derivation of a monoclonal spontaneously immortalized rat Müller cell line (SIRMu-1).
- Characterization using immunofluorescence, western blotting, and RNA sequencing.
- Comparison of SIRMu-1 with primary rat MCs and the transformed rMC-1 cell line.
Main Results:
- SIRMu-1 cells express key Müller cell markers (CRALBP, GS, S100, vimentin, GFAP) at mRNA and protein levels.
- SIRMu-1 exhibits cellular morphology and transcriptome profiles similar to primary rat MCs, more so than rMC-1 cells.
- SIRMu-1 cells demonstrate rapid proliferation, indefinite lifespan, high transfection efficiency, and confirmed male origin.
Conclusions:
- The SIRMu-1 cell line is a valuable experimental tool for investigating Müller cell roles.
- SIRMu-1 offers a more representative model of primary rat Müller cells compared to existing transformed lines.
- This novel cell line can advance research in retinal physiology and pathology.
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