4.8 Article

Loss of Vac14, a regulator of the signaling lipid phosphatidylinositol 3,5-bisphosphate, results in neurodegeneration in mice

Publisher

NATL ACAD SCIENCES
DOI: 10.1073/pnas.0702275104

Keywords

Fab1; PIKfyve; PtdInsl(3,5)P-2; spongiform; endosomal traffic

Funding

  1. NIDDK NIH HHS [P50 DK52617, P50 DK052617] Funding Source: Medline
  2. NIGMS NIH HHS [R01 GM50403, T32 GM07544, R01 GM024872, R01 GM24872, R01 GM050403, T32 GM007544] Funding Source: Medline
  3. NINDS NIH HHS [R01 NS064015] Funding Source: Medline

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The signaling lipid, phosphatidylinositol 3,5-bisphosphate (PI(3,5)P-2), likely functions in multiple signaling pathways. Here, we report the characterization of a mouse mutant lacking Vac14, a regulator of PI(3,S)P-2 synthesis. The mutant mice exhibit massive neurodegeneration, particularly in the midbrain and in peripheral sensory neurons. Cell bodies of affected neurons are vacuolated, and apparently empty spaces are present in areas where neurons should be present. Similar vacuoles are found in cultured neurons and fibroblasts. Selective membrane trafficking pathways, especially endosome-to-TGN retrograde trafficking, are defective. This report, along with a recent report on a mouse with a null mutation in Fig4, presents the unexpected finding that the housekeeping lipid, PI(3,5)P-2, is critical for the survival of neural cells.

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