Your browser doesn't support javascript.
loading
Vasculogenesis in kidney organoids upon transplantation.
Koning, Marije; Dumas, Sébastien J; Avramut, M Cristina; Koning, Roman I; Meta, Elda; Lievers, Ellen; Wiersma, Loes E; Borri, Mila; Liang, Xue; Xie, Lin; Liu, Ping; Chen, Fang; Lin, Lin; Luo, Yonglun; Mulder, Jaap; Spijker, H Siebe; Jaffredo, Thierry; van den Berg, Bernard M; Carmeliet, Peter; van den Berg, Cathelijne W; Rabelink, Ton J.
Afiliação
  • Koning M; Department of Internal Medicine - Nephrology, Leiden University Medical Center, Leiden, the Netherlands.
  • Dumas SJ; Einthoven Laboratory of Vascular and Regenerative Medicine, Leiden University Medical Center, Leiden, the Netherlands.
  • Avramut MC; Laboratory of Angiogenesis and Vascular Metabolism, Department of Oncology and Leuven Cancer Institute (LKI), KU Leuven, VIB Center for Cancer Biology, VIB, Leuven, 3000, Belgium.
  • Koning RI; Department of Cell and Chemical Biology, Leiden University Medical Center, Leiden, the Netherlands.
  • Meta E; Department of Cell and Chemical Biology, Leiden University Medical Center, Leiden, the Netherlands.
  • Lievers E; Laboratory of Angiogenesis and Vascular Metabolism, Department of Oncology and Leuven Cancer Institute (LKI), KU Leuven, VIB Center for Cancer Biology, VIB, Leuven, 3000, Belgium.
  • Wiersma LE; Department of Internal Medicine - Nephrology, Leiden University Medical Center, Leiden, the Netherlands.
  • Borri M; Einthoven Laboratory of Vascular and Regenerative Medicine, Leiden University Medical Center, Leiden, the Netherlands.
  • Liang X; Department of Internal Medicine - Nephrology, Leiden University Medical Center, Leiden, the Netherlands.
  • Xie L; Einthoven Laboratory of Vascular and Regenerative Medicine, Leiden University Medical Center, Leiden, the Netherlands.
  • Liu P; Laboratory of Angiogenesis and Vascular Metabolism, Department of Oncology and Leuven Cancer Institute (LKI), KU Leuven, VIB Center for Cancer Biology, VIB, Leuven, 3000, Belgium.
  • Chen F; Lars Bolund Institute of Regenerative Medicine, Qingdao-Europe Advanced Institute for Life Sciences, BGI-Qingdao, BGI-Shenzhen, Qingdao, China.
  • Lin L; MGI, BGI-Shenzhen, Shenzhen, China.
  • Luo Y; MGI, BGI-Shenzhen, Shenzhen, China.
  • Mulder J; MGI, BGI-Shenzhen, Shenzhen, China.
  • Spijker HS; Department of Biomedicine, Aarhus University, Aarhus, Denmark.
  • Jaffredo T; Steno Diabetes Center Aarhus, Aarhus University Hospital, Aarhus, Denmark.
  • van den Berg BM; Lars Bolund Institute of Regenerative Medicine, Qingdao-Europe Advanced Institute for Life Sciences, BGI-Qingdao, BGI-Shenzhen, Qingdao, China.
  • Carmeliet P; Department of Biomedicine, Aarhus University, Aarhus, Denmark.
  • van den Berg CW; Steno Diabetes Center Aarhus, Aarhus University Hospital, Aarhus, Denmark.
  • Rabelink TJ; Department of Pediatrics, Leiden University Medical Center, Leiden, the Netherlands.
NPJ Regen Med ; 7(1): 40, 2022 Aug 19.
Article em En | MEDLINE | ID: mdl-35986027
ABSTRACT
Human induced pluripotent stem cell-derived kidney organoids have potential for disease modeling and to be developed into clinically transplantable auxiliary tissue. However, they lack a functional vasculature, and the sparse endogenous endothelial cells (ECs) are lost upon prolonged culture in vitro, limiting maturation and applicability. Here, we use intracoelomic transplantation in chicken embryos followed by single-cell RNA sequencing and advanced imaging platforms to induce and study vasculogenesis in kidney organoids. We show expansion of human organoid-derived ECs that reorganize into perfused capillaries and form a chimeric vascular network with host-derived blood vessels. Ligand-receptor analysis infers extensive potential interactions of human ECs with perivascular cells upon transplantation, enabling vessel wall stabilization. Perfused glomeruli display maturation and morphogenesis to capillary loop stage. Our findings demonstrate the beneficial effect of vascularization on not only epithelial cell types, but also the mesenchymal compartment, inducing the expansion of ´on target´ perivascular stromal cells, which in turn are required for further maturation and stabilization of the neo-vasculature. The here described vasculogenic capacity of kidney organoids will have to be deployed to achieve meaningful glomerular maturation and kidney morphogenesis in vitro.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article