Why the study?
The study was conducted to verify the neurotypicality of AAV-PHP.eB after tail vein injection in adult mice and its efficiency in crossing the blood-brain barrier.
AAV-PHP.eB can effectively cross the blood-brain barrier in adult mice, serving as a potential carrier for CNS gene therapy.
May enable systemic CNS gene delivery in adult mice; hypothesis-generating, requires validation in higher species.
Objective To verify the neurotypicality of AAV-PHP.eB after tail vein injection in adult mice and its efficiency in crossing the blood-brain barrier (BBB). Methods The rAAV-SYN-GFP plasmid was constructed, and adult C57BL mice were injected with AAV-PHP. eB: SYN-GFP in the tail vein (300 nL, virus titer 3 × 10 9 vg) and in the prefrontal lobe (50 L, virus titer 5 × 10 11 vg). The green fluorescent protein (GFP) signal in the brain was observed at two weeks, while the GFP signal in the peripheral organs was observed at four weeks. Results Two weeks after tail vein injection, GFP expression was observed throughout the brain, especially in the cortex, hippocampus, and geniculate nucleus. No GFP signal was observed or detected by western blotting in the peripheral organs after four weeks. GFP signal was observed mainly at the local site after prefrontal lobe injection. Conclusion AAV-PHP.eB: SYN-GFP can effectively cross the BBB in adult mice. Using a neuron-specific promoter allows exogenous gene expression in neurons; therefore, AAV-PHP.eB can be used as an effective carrier for studying diseases in the central nervous system (CNS).
No takes yet. Share an insight, caveat, or question.
Shu et al. (2019) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: