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. 2015 Mar 31;10:8. doi: 10.1186/s13064-015-0037-7

Table 1.

Confocal analysis of Fgf lineage cells at E18.5 and P40

Fgf8 CreER/+ Fgf17 CreER/+
Structure Age Marker Double positive/βgal + Double positive/marker + n Double positive/βgal + Double positive/marker + n
Cortex P40 PV (medial) 2% 10% 2 0% 0% 2
P40 PV (lateral) 4% 12% 2 3% 1% 2
P40 SS (medial) 2% 6% 2 0% 0% 2
P40 SS (lateral) 6% 17% 2 0% 0% 2
Septum E18.5 Calbindin 2% 60% 1 17% 23% 1
E18.5 Calretinin 16% 58% 1 24% 19% 1
E18.5 Ctip2 24% 69% 1 15% 9% 1
E18.5 Nkx2.1 5% 74% 1 19% 20% 1
P40 ChAT (MS) 8% 77% 2 17% 33% 4
Diagonal band of Broca E18.5 Calbindin 10% 50% 1 6% 19% 1
E18.5 Nkx2.1 2% 33% 1 9% 26% 1
E18.5 Tbr1 34% 95% 1 59% 41% 1
P40 ChAT 13% 80% 2 28% 44% 4
Striatum P40 ChAT 23% 66% 3 64% 16% 3
P40 Ctip2 70% 9% 3 nd nd nd
P40 PV 1% 14% 2 0% 0% 2
P40 SS 2% 29% 2 nd nd nd
Globus pallidus E18.5 Ctip2 96% 35% 1 71% 3% 1
E18.5 Nkx2.1 92% 37% 1 89% 4% 1
P40 Npas1 72% 28% 3 88% 5% 2
P40 PV 46% 38% 2 0% 0% 2
Nucleus basalis of Meynert P40 ChAT 49% 75% 3 92% 43% 3
Ventral pallidum P40 ChAT 42% 76% 3 95% 45% 3

Quantification of confocal studies examining co-localization of βgal with cell type-specific markers in Fgf8 CreER/+; TauR and Fgf17 CreER/+; TauR animals (Tm E8.5). Parenthetical descriptors (lateral, medial, MS) indicate regional location within the structure. See also Additional file 4: Figures S4 and Additional file 5: Figure S5. Cortical interneuron counts are overestimates, as quantification was done only in regions containing βgal+ cells.