Both promoters are known for broad expression, and the overall transduction patterns that they produced were similar. AAV8-EF1α expression saturated slightly earlier than AAV8-CBA, whereas the latter continued to increase in intensity and extent throughout the first 2 weeks after injection

(Fig. 4). The most notable differences between the two promoters were subtle biases in the pattern of transduction. AAV8-CBA produced slightly more consistent transduction of the neocortex compared with the caudal bias of AAV8-EF1α, whereas AAV8-EF1α was superior in transducing cerebellar Purkinje neurons. Although each combination of serotype and promoter resulted in different transduction patterns IWR-1 ic50 throughout the brain, they all shared a bias towards neuronal expression. Cells expressing virally-delivered YFP or tdTomato could often be identified as neurons based on their morphology and location, and this was further confirmed by immunostaining for the pan-neuronal marker NeuN (9–10 sections/brain from two animals for each serotype, Fig. 4). When intraventricular injection

of AAV1 is delayed past P0, the virus does not transfect brain parenchyma efficiently (Chakrabarty et al., 2010). To determine if the timing of injection similarly affected the pattern of AAV8 transduction, 2.0 × 109 particles/ventricle of AAV8-YFP was injected into the lateral ventricles of littermate

mice at P0, P1, P2 or P3. Mice were then killed after 4 weeks and analysed for transgene this website expression (n = 5 for each condition). Surprisingly, delayed ifenprodil AAV8 injections resulted in substantial transduction throughout the whole brain, although the efficiency decreased at later ages. The transduction attained by P1 injection was nearly identical to that seen after P0 injection. Delayed injection of AAV8 resulted in a diminished spread of virus, particularly in brain structures farthest from the lateral ventricles such as the superficial layers of the cerebral cortex, olfactory bulbs, and cerebellum (Figs 5A, C and E). Interestingly, delayed injection of AAV8 transduced a large number of non-neuronal cells, which rarely occurred following P0 injection (Figs 5B, D and F). The extent of non-neuron transduction increased with the age at injection. Labeled non-neuronal cells were detected in most brain structures with the exception of the olfactory bulb. Immunofluorescence staining for the pan-neuronal marker NeuN confirmed that the majority of cells transduced by AAV8 at P0 were neurons (n = 3, Fig. 5G). Within several areas, including the piriform cortex, amygdala, pons, medulla, and stratum oriens of the hippocampus, a few S100β-positive astrocytes were found expressing the viral label, but these were a small fraction of the transduced cell population (< 1%).