A mechanical pacemaker sets rhythmic nephron formation in the kidney
Description
The mammalian kidney achieves massive parallelization of function by exponentially duplicating nephron-forming niches during development. Each niche caps a tip of the ureteric bud epithelium (the future urinary collecting duct tree) as it undergoes branching morphogenesis, while nephron progenitors within niches balance self-renewal and differentiation to early nephron cells. Nephron formation rate approximately matches branching rate over a large fraction of mouse gestation, yet the nature of this apparent pace-maker is unknown. Here we correlate spatial transcriptomics data with branching ‘life-cycle’ to discover rhythmically alternating signatures of nephron progenitor differentiation and renewal across Wnt, Hippo/Yap, retinoic acid (RA), and other pathways. Our data bring temporal resolution to the renewal vs. differentiation balance in the nephrogenic niche and inform new strategies to achieve self-sustaining nephron formation in synthetic human kidney tissues. tar.gz files correspond to directories containing processed xenium and other data files relating to rhythmic nephron formation in the developing mouse and human kidney. "..._index.xlsx" files within each directory provide brief descriptions of file content and directory organization. "rhythm_Mendeley_supplement_Jan2026_v1.pdf" contains secondary Xenium analyses similar to data in main manuscript Figs. 2C and 3A, but for all human and mouse tissue slices. This data is organized as Figs. M1-M9, which are also provided as full resolution .ai files.
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Institutions
- University of PennsylvaniaPA, Philadelphia