| Literature DB >> 29870722 |
Nils O Lindström1, Guilherme De Sena Brandine2, Tracy Tran1, Andrew Ransick1, Gio Suh1, Jinjin Guo1, Albert D Kim1, Riana K Parvez1, Seth W Ruffins1, Elisabeth A Rutledge1, Matthew E Thornton3, Brendan Grubbs3, Jill A McMahon1, Andrew D Smith4, Andrew P McMahon5.
Abstract
Mammalian nephrons arise from a limited nephron progenitor pool through a reiterative inductive process extending over days (mouse) or weeks (human) of kidney development. Here, we present evidence that human nephron patterning reflects a time-dependent process of recruitment of mesenchymal progenitors into an epithelial nephron precursor. Progressive recruitment predicted from high-resolution image analysis and three-dimensional reconstruction of human nephrogenesis was confirmed through direct visualization and cell fate analysis of mouse kidney organ cultures. Single-cell RNA sequencing of the human nephrogenic niche provided molecular insights into these early patterning processes and predicted developmental trajectories adopted by nephron progenitor cells in forming segment-specific domains of the human nephron. The temporal-recruitment model for nephron polarity and patterning suggested by direct analysis of human kidney development provides a framework for integrating signaling pathways driving mammalian nephrogenesis.Entities:
Keywords: fate; human; kidney; lineage; nephron; patterning; precursor; single-cell; time
Mesh:
Year: 2018 PMID: 29870722 PMCID: PMC6510587 DOI: 10.1016/j.devcel.2018.05.010
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270