Ex Vivo Expanded 3D Human Kidney Spheres Engraft Long Term and Repair Chronic Renal Injury in Mice
Author(s) -
Orit HarariSteinberg,
Dorit Omer,
Yehudit Gnatek,
Oren Pleniceanu,
Sanja Goldberg,
Osnat Cohen-Zontag,
Sara PriChen,
Itamar Kanter,
Nissim Haim,
Eli Becker,
Roi Ankawa,
Yaron Fuchs,
Tomer Kalisky,
Zohar Dotan,
Benjamin Dekel
Publication year - 2020
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2019.12.047
Subject(s) - paracrine signalling , kidney , transplantation , ex vivo , nephron , renal stem cell , kidney disease , biology , progenitor cell , cancer research , kidney transplantation , xenotransplantation , dialysis , renal replacement therapy , pathology , microbiology and biotechnology , immunology , medicine , stem cell , receptor , endocrinology , in vivo
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.
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