Please use this identifier to cite or link to this item:
https://hdl.handle.net/2445/214200
Title: | Natural Hydrogels Support Kidney Organoid Generation and Promote in vitro Angiogenesis |
Author: | Garreta, Elena Moya Rull, Daniel Marco, Andrés Amato, Gaia Ullate Agote, Asier Tarantino, Carolina Gallo, Maria Esporrín Ubieto, David Centeno, Alberto Vilas Zornoza, Amaia Mestre, Rafael Kalil, Maria Gorroñogoitia, Izar Zaldua, Ane Miren Sánchez, Samuel Izquierdo Reyes, Laura Fernández Santos, M. Eugenia Prosper, Felipe Montserrat, Núria |
Keywords: | Angiogènesi Malalties del ronyó Cèl·lules mare Neovascularization Kidney diseases Stem cells |
Issue Date: | 19-May-2024 |
Publisher: | Wiley |
Citation: | E. Garreta, D. Moya-Rull, A. Marco, G. Amato, A. Ullate-Agote, C. Tarantino, M. Gallo, D. Esporrín-Ubieto, A. Centeno, A. Vilas-Zornoza, R. Mestre, M. Kalil, I. Gorroñogoitia, A. M. Zaldua, S. Sanchez, L. I. Reyes, M. E. Fernández-Santos, F. Prosper, N. Montserrat, Natural Hydrogels Support Kidney Organoid Generation and Promote in vitro Angiogenesis. Adv. Mater. 2024, 2400306. https://doi.org/10.1002/adma.202400306 |
Abstract: | To date strategies aiming to modulate cell to extracellular matrix (ECM) interactions during organoid derivation remain largely unexplored. Here renal decellularized extracellular matrix (dECM) hydrogels are fabricated from porcine and human renal cortex as biomaterials to enrich cell-to-ECM crosstalk during the onset of kidney organoid differentiation from human pluripotent stem cells (hPSCs). Renal dECM-derived hydrogels are used in combination with hPSC-derived renal progenitor cells to define new approaches for 2D and 3D kidney organoid differentiation, demonstrating that in the presence of these biomaterials the resulting kidney organoids exhibit renal differentiation features, and the formation of an endogenous vascular component. Based on these observations, a new method to produce kidney organoids with vascular-like structures is achieved through the assembly of hPSC-derived endothelial-like organoids with kidney organoids in 3D. Major readouts of kidney differentiation and renal cell morphology are assessed exploiting these culture platforms as new models of nephrogenesis. Overall, this work shows that exploiting cell-to-ECM interactions during the onset of kidney differentiation from hPSCs facilitates and optimizes current approaches for kidney organoid derivation thereby increasing the utility of these unique culture cell platforms for personalized medicine. |
Note: | Reproducció del document publicat a: https://doi.org/10.1002/adma.202400306 |
It is part of: | Advanced Materials, 2024, vol. 36 |
URI: | https://hdl.handle.net/2445/214200 |
Related resource: | https://doi.org/10.1002/adma.202400306 |
DOI: | https://doi.org/10.1002/adma.202400306 |
ISSN: | 1521-4095 |
Appears in Collections: | Articles publicats en revistes (Institut de Bioenginyeria de Catalunya (IBEC)) |
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AdvancedMaterials2024Garreta.pdf | 10.16 MB | Adobe PDF | View/Open |
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