From: Stable, neuron-specific gene expression in the mouse brain
Methods for transgene delivery into the mouse brain | |||||
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Gene delivery method | Routes | Expression regions | Advantages | Disadvantages | References |
Retro-orbital injection | Retina | Retina and brain | Direct route to the brainbypassing the BBB; efficient and effective for delivering drugs | Disruptive to the pups; potential vision damage; possible anesthesia's systemic effect; special training on anaesthetization | |
Intravenous injection | Tail vein | Brain and other tissues | No special equipment needed | Injected substance needs to be able to cross the BBB; larger volumes of virus needs; low transgene expression; diffusion to other tissues; laborious to perform; high failure rate | [3] |
In-vivo electroporation | Ventricle/desired brain parenchyma | Whole brain or specific brain region | Direct delivery of DNA; strong expression of transgenes; rapid and efficient | Need optimization; specialized voltage for widespread delivery; high cost; germline modifications; surgical procedures | |
Intravascular injection | Temporal facial vein | CNS and peripheral organs | Stable and global transgene expression; efficient; minimal stress and quick recovery | Specialized handling skill; possible damage to BBB; injected substance needs to be able to cross the BBB | [15] |
Transverse sinus | Transverse sinus | Whole brain | Efficient; fast and simple; less equipment | Specialized handling skill; not enough applications | [14] |
Intracerebroventricular injection | Ventricular system | Whole brain | Can be adapted for cell type-specific expression; direct delivery into the mouse brain; no need to cross the BBB; cost-effective; rapid; no surgery needed; no undesirable side effects in neonatal mice; quick recovery in neonatal mice | Non-uniform expression across the brain | Current study |