| Literature DB >> 31968258 |
Orit Harari-Steinberg1, Dorit Omer1, Yehudit Gnatek1, Oren Pleniceanu1, Sanja Goldberg1, Osnat Cohen-Zontag1, Sara Pri-Chen2, Itamar Kanter3, Nissim Ben Haim3, Eli Becker3, Roi Ankawa4, Yaron Fuchs4, Tomer Kalisky3, Zohar Dotan5, Benjamin Dekel6.
Abstract
End-stage renal disease is a worldwide epidemic requiring renal replacement therapy. Harvesting tissue from failing kidneys and autotransplantation of tissue progenitors could theoretically delay the need for dialysis. Here we use healthy and end-stage human adult kidneys to robustly expand proliferative kidney epithelial cells and establish 3D kidney epithelial cultures termed "nephrospheres." Formation of nephrospheres reestablishes renal identity and function in primary cultures. Transplantation into NOD/SCID mice shows that nephrospheres restore self-organogenetic properties lost in monolayer cultures, allowing long-term engraftment as tubular structures, potentially adding nephron segments and demonstrating self-organization as critical to survival. Furthermore, long-term tubular engraftment of nephrospheres is functionally beneficial in murine models of chronic kidney disease. Remarkably, nephrospheres inhibit pro-fibrotic collagen production in cultured fibroblasts via paracrine modulation, while transplanted nephrospheres induce transcriptional signatures of proliferation and release from quiescence, suggesting re-activation of endogenous repair. These data support the use of human nephrospheres for renal cell therapy.Entities:
Keywords: 3D culture; 5/6 nephrectomy; antifibrotic effect; autologous treatment; in vivo differentiation; kidney regeneration; kidney stem cells; mouse CKD model; nephrospheres; renal epithelial differentiation
Mesh:
Year: 2020 PMID: 31968258 DOI: 10.1016/j.celrep.2019.12.047
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423