4.6 Article

Critical Role for Phosphatidylinositol-3 Kinase Vps34/PIK3C3 in ON-Bipolar Cells

期刊

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
卷 60, 期 8, 页码 2861-2874

出版社

ASSOC RESEARCH VISION OPHTHALMOLOGY INC
DOI: 10.1167/iovs.19-26586

关键词

bipolar cell; Vps34; autophagy; phosphoinositide; degeneration

资金

  1. NIH [R01-EY025218, R01-EY026545]
  2. Welch Foundation [Q0035]
  3. Core Grant for Vision Research from the National Eye Institute (Bethesda, MD, USA) [P30 EY002520]
  4. Intellectual and Developmental Disabilities Research Center Grant from the Eunice Kennedy Shriver National Institute of Child Health & Human Development [U54 HD083092]
  5. NATIONAL EYE INSTITUTE [P30EY002520] Funding Source: NIH RePORTER

向作者/读者索取更多资源

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.

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