VAPB depletion alters neuritogenesis and phosphoinositide balance in motoneuron-like cells: relevance to VAPB-linked amyotrophic lateral sclerosis.

Abstract

VAPB and VAPA are ubiquitously expressed endoplasmic reticulum membrane proteins that play key roles in lipid exchange at membrane contact sites. A mutant, aggregation-prone, form of VAPB (P56S) is linked to a dominantly inherited form of amyotrophic lateral sclerosis; however, it has been unclear whether its pathogenicity is due to toxic gain of function, to negative dominance, or simply to insufficient levels of the wild-type protein produced from a single allele (haploinsufficiency). To investigate whether reduced levels of functional VAPB, independently from the presence of the mutant form, affect the physiology of mammalian motoneuron-like cells, we generated NSC34 clones, from which VAPB was partially or nearly completely depleted. VAPA levels, determined to be over fourfold higher than those of VAPB in untransfected cells, were unaffected. Nonetheless, cells with even partially depleted VAPB showed an increase in Golgi- and acidic vesicle-localized phosphatidylinositol-4-phosphate (PI4P) and reduced neurite extension when induced to differentiate. Conversely, the PI4 kinase inhibitors PIK93 and IN-10 increased neurite elongation. Thus, for long-term survival, motoneurons might require the full dose of functional VAPB, which may have unique function(s) that VAPA cannot perform.

• Authors: Paola Genevini, Maria Nicol Colombo, Rossella Venditti, Stefania Marcuzzo, Sara Francesca Colombo, Pia Bernasconi, Maria Antonietta De Matteis, Nica Borgese, Francesca Navone
• Journal: Journal of cell science (J Cell Sci) Vol. 132 Issue 7 (04 03 2019) ISSN: 1477-9137 [Electronic] England
• PMID: 30745341 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: © 2019. Published by The Company of Biologists Ltd.

Chemical References

• Phosphatidylinositols
• VAPB protein, human
• Vesicular Transport Proteins

Topics

• Amyotrophic Lateral Sclerosis (genetics, metabolism, pathology)
• Animals
• Endoplasmic Reticulum (metabolism)
• Golgi Apparatus (metabolism)
• HeLa Cells
• Humans
• Motor Neurons (metabolism, pathology)
• Mutation
• Neurites (metabolism, pathology)
• Phosphatidylinositols (metabolism)
• Rats
• Vesicular Transport Proteins (genetics, metabolism)