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Repair after nephron ablation reveals limitations of neonatal neonephrogenesis
Florian Tögel, M. Todd Valerius, Benjamin S. Freedman, Rossella Iatrino, Mor Grinstein, Joseph V. Bonventre
Florian Tögel, M. Todd Valerius, Benjamin S. Freedman, Rossella Iatrino, Mor Grinstein, Joseph V. Bonventre
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Research Article Development Nephrology

Repair after nephron ablation reveals limitations of neonatal neonephrogenesis

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Abstract

The neonatal mouse kidney retains nephron progenitor cells in a nephrogenic zone for 3 days after birth. We evaluated whether de novo nephrogenesis can be induced postnatally beyond 3 days. Given the long-term implications of nephron number for kidney health, it would be useful to enhance nephrogenesis in the neonate. We induced nephron reduction by cryoinjury with or without contralateral nephrectomy during the neonatal period or after 1 week of age. There was no detectable compensatory de novo nephrogenesis, as determined by glomerular counting and lineage tracing. Contralateral nephrectomy resulted in additional adaptive healing, with little or no fibrosis, but did not also stimulate de novo nephrogenesis. In contrast, injury initiated at 1 week of age led to healing with fibrosis. Thus, despite the presence of progenitor cells and ongoing nephron maturation in the newborn mouse kidney, de novo nephrogenesis is not inducible by acute nephron reduction. This indicates that additional nephron progenitors cannot be recruited after birth despite partial renal ablation providing a reparative stimulus and suggests that nephron number in the mouse is predetermined at birth.

Authors

Florian Tögel, M. Todd Valerius, Benjamin S. Freedman, Rossella Iatrino, Mor Grinstein, Joseph V. Bonventre

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Figure 5

Lineage tracing to determine nephron formation.

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Lineage tracing to determine nephron formation.
(A) Breeding strategy of...
(A) Breeding strategy of transgenic animals. Six2 heterozygous (Six2GCE/+) mice were crossed to tdTomato reporter (R26RtdTomato/tdTomato) mice. Injury was induced on the day of birth (P1) followed by tamoxifen injection to induce recombination in Six2+ cells. Kidneys were harvested at P7. tdTomato is expressed permanently in all cells that were Six2+ at the time of tamoxifen injection and their daughter cells. (B) Negative controls injected with tamoxifen at E17.5 showed no recombination, as expected (left). Positive controls injected at E17.5 had approximately 50% of nephrons labeled positive with tdTomato (middle). Animals injected with tamoxifen at P1 had 46% of glomeruli labeled by tdTomato (right). Original magnification, ×4. (C) Podocalyxin staining in combination with tdTomato fluorescence was used to determine the number of tdTomato-labeled glomeruli as surrogate number for labeled nephrons. An overview of a kidney with the red channel on the left side (tdTomato) and the far-red channel (podocalyxin) on the right side (left). Higher-magnification images showing two dual-labeled (tdTomato and podocalyxin) glomeruli (arrowheads) as well as several non-tdTomato-labeled glomeruli. Original magnification left panel, ×4; right panel, ×20. (D) The percentage of tdTomato-labeled glomeruli was not significantly different in animals subjected to cryoinjury (left) compared with uninjured control animals (right). Original magnification, ×4. (E) When tamoxifen was injected at P3 in animals subjected to cryoinjury, we found only single dispersed tdTomato+ cells in the outer cortex. Original magnification, ×10. (F) Determination of tdTomato-labeled glomeruli was done using podocalyxin staining (green). Double-labeled glomeruli (podocalyxin and tdTomato) appear yellow (left). The percentage of tdTomato-labeled glomeruli was not significantly different after injury compared with control animals or contralateral control kidneys (right panel). Original magnification, ×4. n = 6 animals per group. In box-and-whisker plots, whiskers depict the minimum and maximum values, boxes depict 25th to 75th percentiles, and lines depict the median. Ordinary 1-way ANOVA, Tukey’s multiple comparison test.

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