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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 3

No increase in proliferation with cryoablation.

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No increase in proliferation with cryoablation.
(A) Numbers of prolifera...
(A) Numbers of proliferating cells (Ki67 positive, red) were not different around injured areas compared with remote cortical areas of the injured or contralateral control kidneys as well as sham animals of the same age. Original magnification, ×20. LTL+ proximal tubules, green. (B) Analysis of the number of proliferating cells per high-power field (original magnification, ×20) was done at P3, P4, P6, and P8 and showed no significant difference between injured kidneys, sham operated kidneys, or contralateral control kidneys (10 high-power fields, n = 3–5 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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