Resumen
PURPOSE. Phosphatidylinositol-3-phosphate (PI(3)P), and Vps34, the type III phosphatidylinositol 3-kinase primarily responsible for its production, are important for function and survival of sensory neurons, where they have key roles in membrane processing events, such as autophagy, endosome processing, and fusion of membranes bearing ubiquitinated cargos with lysosomes. We examined their roles in the most abundant class of secondary neurons in the vertebrate retina, the ON-bipolar cells (ON-BCs). METHODS. A conditional Vps34 knockout mouse line was generated by crossing Vps34 floxed mice with transgenic mice expressing Cre recombinase in ON-BCs. Structural changes in the retina were determined by immunofluorescence and electron microscopy, and bipolar cell function was determined by electroretinography. RESULTS. Vps34 deletion led to selective death of ON-BCs, a thinning of the inner nuclear layer, and a progressive decline of electroretinogram b-wave amplitudes. There was no evidence for loss of other retinal neurons, or disruption of rod-horizontal cell contacts in the outer plexiform layer. Loss of Vps34 led to aberrant accumulation of membranes positive for autophagy markers LC3, p62, and ubiquitin, accumulation of endosomal membranes positive for Rab7, and accumulation of lysosomes. Similar effects were observed in Purkinje cells of the cerebellum, leading to severe and progressive ataxia. CONCLUSIONS. These results support an essential role for PI(3)P in fusion of autophagosomes with lysosomes and in late endosome maturation. The cell death resulting from Vps34 knockout suggests that these processes are essential for the health of ON-BCs.
Idioma original | English |
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Páginas (desde-hasta) | 2861-2874 |
Número de páginas | 14 |
Publicación | Investigative Ophthalmology and Visual Science |
Volumen | 60 |
N.º | 8 |
DOI | |
Estado | Published - jul. 2019 |
Publicado de forma externa | Sí |
Nota bibliográfica
Funding Information:The authors thank Ching-Kang Jason Chen (Baylor College of Medicine) for training in ERG recordings. Supported by NIH Grants R01-EY025218 and R01-EY026545 and by the Welch Foundation, Q0035 (TGW). The ERG and EM facilities are supported by Core Grant for Vision Research P30 EY002520 from the National Eye Institute (Bethesda, MD, USA). The Neurobehavioral Core is supported by Intellectual and Developmental Disabilities Research Center Grant U54 HD083092 from the Eunice Kennedy Shriver National Institute of Child Health & Human Development.
Funding Information:
Supported by NIH Grants R01-EY025218 and R01-EY026545 and by the Welch Foundation, Q0035 (TGW). The ERG and EM facilities are supported by Core Grant for Vision Research P30 EY002520 from the National Eye Institute (Bethesda, MD, USA). The Neurobehavioral Core is supported by Intellectual and Developmental Disabilities Research Center Grant U54 HD083092 from the Eunice Kennedy Shriver National Institute of Child Health & Human Development.
Publisher Copyright:
© 2019 The Authors.
ASJC Scopus Subject Areas
- Ophthalmology
- Sensory Systems
- Cellular and Molecular Neuroscience