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. 2020 Nov 16;473(1):79–93. doi: 10.1007/s00424-020-02491-1

Fig. 1.

Fig. 1

Characterization of NCC-cre-ERT2 mice. A Schematic representation of insertion of the tamoxifen-inducible creERT2 in the untranslated region (UTR) of the last exon of the Slc12a3/NCC gene. B Immunostaining for NCC, cre, and calbindin D28K (CB28) on consecutive cryosections from NCC-cre-ERT2 mice. Tamoxifen induces strong nuclear localization of the cre recombinase in NCC-positive DCT1 (1) and in DCT2 (2) with strong NCC and CB28-immunostaining. C Overviews on kidneys from NCC-cre-ERT2/tomato-flox mice (upper panel) show a strong tomato-related fluorescence in a kidney of tamoxifen-induced but not in the kidney of an uninduced mouse. High-power magnification (lower panel) demonstrate that the tomato-related fluorescence is strictly limited to the DCT (D) and is not found in the preceding NKCC2-positive TAL (T) and the downstream localized AQP2-positive CNT (CN). The segment transitions are indicated by double-headed arrows. Two pairs of consecutive cryosections. D and E Immunoblots and densitometry reveal that the creERT2 transgene does not interfere with NCC abundance and phosphorylation. Data are mean ± SEM, n = 3