Augmented and accelerated nephrogenesis in TGF-beta2 heterozygous mutant mice

Sunder Sims-Lucus, Georgina Caruana, John P Dowling, Michelle Monica Kett, John Frederick Bertram

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Several members of the transforming growth factor-beta (TGF-beta) super family play key roles in kidney development, either directly or indirectly regulating nephron number. Whilst low nephron number is a risk factor for cardiovascular and renal disease, the implications of increased nephron number has not been examined due to the absence of appropriate animal models. Here, using unbiased stereology we demonstrated that kidneys from TGF-beta2 heterozygous (TGF-beta2) mice have approximately 60 more nephrons than wild type (WT) mice at postnatal day 30 (P30). To determine if augmented nephron number involved accelerated ureteric branching morphogenesis, embryonic day 11.5 (E11.5) metanephroi were analyzed via confocal microscopy. A 40 increase in total ureteric branch length was observed in TGF-beta2 kidneys, together with an extra generation of branching. In E12.5 metanephroi cultured for 48 hours the numbers of both ureteric tree tips and glomeruli were significantly greater in TGF-beta2 kidneys. These findings suggest that augmented nephron number in TGF-beta2+/- kidneys results from accelerated ureteric branching morphogenesis and nephron formation. Manipulation of TGF-beta2 signaling in vivo may provide avenues for protection or rescue of nephron endowment in fetuses at risk.
Original languageEnglish
Pages (from-to)607 - 612
Number of pages6
JournalPediatric Research
Issue number6
Publication statusPublished - 2008

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