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Updated: Aug 11, 2026

Dissection and Culture of Mouse Embryonic Kidney
Published on: May 17, 2017
Developmental changes in the expression of tight junction protein claudins in murine metanephroi and embryonic
Hiroshi Ohta1, Hirokazu Adachi, Mutsumi Inaba
1Laboratory of Molecular Medicine, Department of Veterinary Clinical Sciences, Graduate School of Veterinary Medicine, Hokkaido University, Sapporo 060-0818, Japan.
Abstract:
Claudins are the major constituents of tight junction (TJ) strands and participate in the cell-cell adhesion and permeability barrier in epithelial cell layers. To investigate the suitability of metanephroi for analysis of the function of the TJ protein claudins in renal tubular formation, mouse metanephroi from embryos at day 12 of gestation were cultured and expression of claudins was compared with that in embryonic kidneys. During in vitro culture for 8 days, the metanephroi showed expression patterns very similar to those observed in embryonic kidneys in reverse transcription-polymerase chain reaction for the claudins examined, including claudins 1-4, 8, 10, 11, and 16, and the TJ proteins occludin and ZO-1. Immunofluorescence microscopy for claudins 1-4, 8, 10, and 16 showed localization of these claudins at the TJ with occludin and ZO-1 in some restricted tubular segments. These findings indicate that the metanephroi show developmental changes in the expression of the TJ protein claudins, representing those in embryonic kidneys, and thus suggest that the mouse metanephros is suitable to examine the functions of specific claudins in the kidney.
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