Disparate levels of beta-catenin activity determine nephron progenitor cell fate

Harini Ramalingam, Alicia R. Fessler, Amrita Das, M. Todd Valerius, Jeannine Basta, Lynn Robbins, Aaron C. Brown, Leif Oxburgh, Andrew P. McMahon, Michael Rauchman, Thomas J. Carroll

Research output: Contribution to journalArticlepeer-review

19 Scopus citations


Formation of a functional kidney depends on the balance between renewal and differentiation of nephron progenitors. Failure to sustain this balance can lead to kidney failure or stem cell tumors. For nearly 60 years, we have known that signals from an epithelial structure known as the ureteric bud were essential for maintaining this balance. More recently it was discovered that one molecule, Wnt9b, was necessary for both renewal and differentiation of the nephron progenitor cells. How one ligand signaling through one transcription factor promoted two seemingly contradictory cellular processes was unclear. In this study, we show that Wnt9b/beta-catenin signaling alone is sufficient to promote both renewal and differentiation. Moreover, we show that discrete levels of beta-catenin can promote these two disparate fates, with low levels fostering progenitor renewal and high levels driving differentiation. These results provide insight into how Wnt9b regulates distinct target genes that balance nephron progenitor renewal and differentiation.

Original languageEnglish
Pages (from-to)13-21
Number of pages9
JournalDevelopmental Biology
Issue number1
StatePublished - Aug 1 2018


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