Abstract
Generating kidney organoids using human stem cells could offer promising prospects for research and therapeutic purposes.However, no cell-based strategy has generated nephrons displaying an intact threedimensional epithelial filtering barrier. Here, we generated organoids using murine embryonic kidney cells, and documented that these tissues recapitulated the complex three-dimensional filtering structure of glomerular slits in vivo and accomplished selective glomerular filtration and tubular reabsorption. Exploiting this technology, we mixed human amniotic fluid stem cells with mouse embryonic kidney cells to establish three-dimensional chimeric organoids that engrafted in vivo and grew to form vascularized glomeruli and tubular structures. Human cells contributed to the formation of glomerular structures, differentiated into podocytes with slit diaphragms, and internalized exogenously infused BSA, thus attaining in vivo degrees of specialization and function unprecedented for donor stem cells. In conclusion, human amniotic fluid stem cell chimeric organoids may offer new paths for studying renal development and human podocyte disease, and for facilitating drug discovery and translational research.
| Original language | English |
|---|---|
| Pages (from-to) | 1400-1411 |
| Number of pages | 12 |
| Journal | Journal of the American Society of Nephrology |
| Volume | 27 |
| Issue number | 5 |
| DOIs | |
| Publication status | Published - May 2016 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
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