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Merck
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  • The generation of kidney organoids by differentiation of human pluripotent cells to ureteric bud progenitor-like cells.

The generation of kidney organoids by differentiation of human pluripotent cells to ureteric bud progenitor-like cells.

Nature protocols (2014-10-24)
Yun Xia, Ignacio Sancho-Martinez, Emmanuel Nivet, Concepcion Rodriguez Esteban, Josep Maria Campistol, Juan Carlos Izpisua Belmonte
摘要

This protocol presents recently developed methodologies for the differentiation of human pluripotent stem cells (hPSCs) into ureteric bud (UB) progenitor-like cells. Differentiation of human PSCs to UB progenitor-like cells allows for the generation of chimeric kidney cultures in which the human cells can self-assemble into chimeric 3D structures in combination with embryonic mouse kidney cells over a period of 18 d. UB progenitor-like cells are generated by a two-step process that combines in vitro commitment of human PSCs, whether embryonic stem cells (ESCs) or induced PSCs (iPSCs), under chemically defined culture conditions, with ex vivo cultures for the induction of 3D organogenesis. The models described here provide new opportunities for investigating human kidney development, modeling disease, evaluating regenerative medicine strategies, as well as for toxicology studies.

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Sigma-Aldrich
胰岛素 溶液 人, sterile-filtered, BioXtra, suitable for cell culture
Roche
重组DNase I,无RNase, from bovine pancreas, expressed in Pichia pastoris
Sigma-Aldrich
甘氨酸, suitable for electrophoresis, ≥99%
Sigma-Aldrich
全转铁蛋白 人, powder, BioReagent, suitable for cell culture, ≥97%
Sigma-Aldrich
亚硒酸钠, BioReagent, suitable for cell culture, ≥98%
Sigma-Aldrich
γ-氨基丁酸, ≥99%
Sigma-Aldrich
抗核抗体,克隆235-1, clone 235-1, Chemicon®, from mouse