Novel insights into pathomechanisms of retinal neuronal degeneration and reactive gliosis in a murine model of GM1-gangliosidosis

Sci Rep. 2025 Aug 13;15(1):29674. doi: 10.1038/s41598-025-15639-9.

Abstract

GM1-gangliosidosis is a lysosomal storage disease characterized by the accumulation of GM1 ganglioside in neurons, including retinal ganglion cells (RGCs). Although vision impairment and retinal degeneration are well-known manifestations in humans, knowledge about the underlying mechanism of these lesions is limited. Pathological retinal changes in a Glb1 knockout (Glb1-/-) mouse model were assessed using immunohistochemistry, immunofluorescence and transmission electron microscopy in 4- and 7-month-old wild type and Glb1 knockout (Glb1-/-) mice. Increased numbers of glial fibrillary acidic protein (GFAP) positive Müller cells (MCs) were detected in Glb1-/- mice both at 4 and 7 months of age, indicating glial reactivity. A transient increase in glutamine synthetase (GS) positive MCs at 4 months of age with a subsequent decrease by 7 months, most likely related to reduced expression of GS, was also observed. Immunohistochemistry revealed loss of RGCs, storage material accumulation and decreased BRN3A expression in 7-month-old Glb1-/- mice. Increasing numbers of Iba1-positive microglia/macrophages were detected in Glb1-/- mice at both time points. Microglia/macrophages showed migration towards the inner retinal layers and acquired a morphological phenotype that indicates activation. The present study shows that the murine GM1 model used in this study is suitable for investigating ocular changes in lysosomal storage diseases.

Keywords: GM1 accumulation; GM1-gangliosidosis; Lysosomal storage disease; Microglia activation; Müller cells; Retinal gliosis; Retinal pathology.

MeSH terms

  • Animals
  • Disease Models, Animal
  • Ependymoglial Cells / metabolism
  • Ependymoglial Cells / pathology
  • Gangliosidosis, GM1* / complications
  • Gangliosidosis, GM1* / genetics
  • Gangliosidosis, GM1* / metabolism
  • Gangliosidosis, GM1* / pathology
  • Glial Fibrillary Acidic Protein / metabolism
  • Gliosis* / metabolism
  • Gliosis* / pathology
  • Glutamate-Ammonia Ligase / genetics
  • Glutamate-Ammonia Ligase / metabolism
  • Mice
  • Mice, Knockout
  • Microglia / metabolism
  • Microglia / pathology
  • Retina / metabolism
  • Retina / pathology
  • Retinal Degeneration* / genetics
  • Retinal Degeneration* / metabolism
  • Retinal Degeneration* / pathology
  • Retinal Ganglion Cells / metabolism
  • Retinal Ganglion Cells / pathology

Substances

  • Glutamate-Ammonia Ligase
  • Glial Fibrillary Acidic Protein