Reversion of the biochemical defects in murine embryonic Sandhoff neurons using a bicistronic lentiviral vector encoding hexosaminidase α and β

Sandhoff disease, a neurodegenerative disorder characterized by the intracellular accumulation of GM2 ganglioside, is caused by mutations in the hexosaminidase β‐chain gene resulting in a hexosaminidase A (αβ) and B (ββ) deficiency. A bicistronic lentiviral vector encoding both the hexosaminidase α and β chains (SIV.ASB) has previously been shown to correct the β‐hexosaminidase deficiency and to reduce GM2 levels both in transduced and cross‐corrected human Sandhoff fibroblasts. Recent advances in determining the neuropathophysiological mechanisms in Sandhoff disease have shown a mechanistic link between GM2 accumulation, neuronal cell death, reduction of sarcoplasmic/endoplasmic reticulum Ca 2+ ‐ATPase (SERCA) activity, and axonal outgrowth. To examine the ability of the SIV.ASB vector to reverse these pathophysiological events, hippocampal neurons from embryonic Sandhoff mice were transduced with the lentivector. Normal axonal growth rates were restored, as was the rate of Ca 2+ uptake via the SERCA and the sensitivity of the neurons to thapsigargin‐induced cell death, concomitant with a decrease in GM2 and GA2 levels. Thus, we have demonstrated that the bicistronic vector can reverse the biochemical defects and down‐stream consequences in Sandhoff neurons, reinforcing its potential for Sandhoff disease in vivo gene therapy.