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. 2015 May 20;35(20):7878–7891. doi: 10.1523/JNEUROSCI.2179-14.2015

Table 1.

Timeline of experiments and analysis

Pou4f3 expression
    Tissue collected P2, P5, P22, and P75
    Analysis Cochlea and brainstem tissue labeled for Pou4f3
Hair cell survival in vitro
    Age harvested P2–P3
    Time in culture before treatment 24 h
    Days of treatment before fixing 3
    Analysis Cultured cochlea labeled and imaged
Neonatal in vivo (cochlear, SGN, and CN changes)
    Age at time of DT injection P2 (4 ng/g) or P5 (5 ng/g)
    Tissue collected 2, 4, 6–8, 10, 14, 21, and 70+ dpi
    Analysis Cochlea labeled and hair cells counted, Rosenthal's canal labeled and SGNs counted, cochlear nucleus labeled and neurons counted
Mature in vivo (ABR testing)
    Age at time of DT injection P28–P35 (25 ng/g)
    Mice tested Immediately before and 1, 3, 5, 8, and 21 dpi
    Tissue collected Immediately after ABR testing at each time point
    Analysis ABR threshold identified, cochlea labeled, and hair cells counted
Mature in vivo (dose response)
    Age at time of DT injection P30–P42 (5, 15, or 25 ng/g)
    Tissue collected 8 and 21 dpi
    Analysis Cochlea labeled and hair cells counted
Mature in vivo (cochlear, SGN, and CN changes)
    Age at time of DT injection P21–P42 (25 ng/g)
    Tissue collected 2, 4, 6–8, 10, 14, 21, and 70+ dpi
    Analysis Cochlea labeled and hair cells counted, Rosenthal's canal labeled and SGNs counted, cochlear nucleus labeled and neurons counted