Direct Isolation and Characterization of Human Nephron Progenitors

Author:

Da Sacco Stefano1,Thornton Matthew E.2,Petrosyan Astgik1,Lavarreda-Pearce Maria1,Sedrakyan Sargis1,Grubbs Brendan H.2,De Filippo Roger E.13,Perin Laura13

Affiliation:

1. a GOFARR Laboratory for Organ Regenerative Research and Cell Therapeutics, Saban Research Institute, Division of Urology, Children's Hospital Los Angeles, Los Angeles, California, USA

2. b Maternal-Fetal Medicine Division, Department of Obstetrics and Gynecology, Keck School of Medicine, University of Southern California, Los Angeles, California, USA

3. c Department of Urology, Keck School of Medicine, University of Southern California, Los Angeles, California, USA

Abstract

Abstract Mature nephrons originate from a small population of uninduced nephrogenic progenitor cells (NPs) within the cap mesenchyme. These cells are characterized by the coexpression of SIX2 and CITED1. Many studies on mouse models as well as on human pluripotent stem cells have advanced our knowledge of NPs, but very little is known about this population in humans, since it is exhausted before birth and strategies for its direct isolation are still limited. Here we report an efficient protocol for direct isolation of human NPs without genetic manipulation or stepwise induction procedures. With the use of RNA-labeling probes, we isolated SIX2+CITED1+ cells from human fetal kidney for the first time. We confirmed their nephrogenic state by gene profiling and evaluated their nephrogenic capabilities in giving rise to mature renal cells. We also evaluated the ability to culture these cells without complete loss of SIX2 and CITED1 expression over time. In addition to defining the gene profile of human NPs, this in vitro system facilitates studies of human renal development and provides a novel tool for renal regeneration and bioengineering purposes.

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,General Medicine

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