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  • Projects
    • Project 1 - Development of a Gene Therapy for Usher Syndrome Type 1B (USH1B)
    • Project 2 - Evaluation of novel gene therapy approaches for USH2A
    • Project 3 - Retina organoids as models for assessing pathomechanisms and effects of novel treatments inn retinal disorders
    • Project 4 - Development of a one-time gene therapy for age-related macular degeneration
    • Project 5 - Development of novel gene therapy strategies for treatment of autosomal dominant retinitis pigmentosa in a pig model
    • Project 6 - Novel targets for gene therapy in diabetic retinopathy (DR)
    • Project 7 - RPE plasticity in the context of neurodegenerative disease: Understanding the limits, pushing the boundaries
    • Project 8 - Novel AI-based biomarkers for retinal gene therapy outcomes by integrating functional neuroimaging and retinal imaging
    • Project 9 - Integrating imaging, clinical and genetic data with machine learning to establish biomarkers for retinal diseases
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  1. DFG-Forschergruppe 5621
  2. Publications
  3. Müller cells trophism and pathology as the next therapeutic targets for retinal diseases
press releases | 23/04/2025
Project 6

Müller cells trophism and pathology as the next therapeutic targets for retinal diseases

Review by Arregio et al. in Progress in Retinal and Eye Research
PMID: 40254246 DOI: https://doi.org/10.1016/j.preteyeres.2025.101357

Highlights:

• Preserving Müller cells trophism is essential, as Müller cells are a major cell type in the retina to maintain retinal structure, metabolism, and homeostasis.

• Müller cells play a key role in retinal diseases and their dysfunction - discussed here as Müller cells pathology - drives degenerative processes.

• “Müllerotrophism” and “Mülleropathy” should be considered new major therapeutic targets for retinal diseases.

  • Pubmed entry

All DFG-Forschergruppe 5621 Press Releases

FOR 5621 Research unit

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