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. 2011 Aug 10;31(32):11587–11596. doi: 10.1523/JNEUROSCI.0614-11.2011

Table 1.

Expression patterns of fluorescent proteins in the glomerular layer in transgenic mouse lines used in this study

Markers VGAT-Venus
TH-Cre;Rosa26R-CFP
TH-GFP
Marker+ [%] Venus+ [%] Marker+ [%] CFP+ [%] Marker+ [%] GFP+ [%]
TH 20.0 ± 0.3 98.1 ± 0.7 72.1 ± 1.5 64.5 ± 1.1 82.7 ± 1.4 98.1 ± 0.6
(n = 2120) (n = 432) (n = 1571) (n = 1762) (n = 804) (n = 676)
CB 15.0 ± 0.3 98.9 ± 0.2 0 ± 0 0 ± 0 0.27 ± 0.1 0.57 ± 0.3
(n = 2274) (n = 344) (n = 713) (n = 404) (n = 760) (n = 350)
CR 34.5 ± 3.2 79.5 ± 3.9 0.13 ± 0.1 0.05 ± 0.1 0 ± 0 0 ± 0
(n = 1142) (n = 495) (n = 763) (n = 1943) (n = 368) (n = 934)
GAD67 99.4 ± 0.2 99.2 ± 0.2 98.5 ± 0.03 19.0 ± 0.2 95.1 ± 0.7 22.9 ± 1.2
(n = 1166) (n = 1169) (n = 783) (n = 4055) (n = 362) (n = 1508)

The table shows the percentage of fluorescently-labeled PGCs that expressed TH, CB, CR, or the GABAergic neuron marker, GAD67 (Marker+ [%]) and the percentage of PGCs expressing each neuronal marker that also expressed a fluorescent protein (Venus+, CFP+, or GFP+ [%]). Both TH−/CFP + cells in TH-Cre;Rosa26R-CFP and TH−/GFP + cells in TH-GFP mice express Pax6 (100 ± 0% and 95.7 ± 0.8%, respectively), which is an early marker for DAergic PGC differentiation (Hack et al., 2005; Kohwi et al., 2005; Haba et al., 2009), but not CB or CR, suggesting that they are immature DAergic PGCs. “n” indicates the number of cells (from three animals) analyzed here.