Your browser doesn't support javascript.
loading
A microfluidic platform integrating functional vascularized organoids-on-chip.
Quintard, Clément; Tubbs, Emily; Jonsson, Gustav; Jiao, Jie; Wang, Jun; Werschler, Nicolas; Laporte, Camille; Pitaval, Amandine; Bah, Thierno-Sidy; Pomeranz, Gideon; Bissardon, Caroline; Kaal, Joris; Leopoldi, Alexandra; Long, David A; Blandin, Pierre; Achard, Jean-Luc; Battail, Christophe; Hagelkruys, Astrid; Navarro, Fabrice; Fouillet, Yves; Penninger, Josef M; Gidrol, Xavier.
Affiliation
  • Quintard C; Univ. Grenoble Alpes, CEA, IRIG/BGE, BIOMICS, 38000, Grenoble, France.
  • Tubbs E; Univ. Grenoble Alpes, CEA, LETI, DTBS, 38000, Grenoble, France.
  • Jonsson G; Department of Medical Genetics, Life Sciences Institute, University of British Columbia, Vancouver, British Columbia (BC), Canada.
  • Jiao J; Univ. Grenoble Alpes, CEA, IRIG/BGE, BIOMICS, 38000, Grenoble, France.
  • Wang J; Institute of Molecular Biotechnology of the Austrian Academy of Sciences, IMBA, Dr. Bohr-Gasse 3, 1030, Vienna, Austria.
  • Werschler N; Vienna BioCenter PhD Program, Doctoral School of the University of Vienna and Medical University of Vienna, 1030, Vienna, Austria.
  • Laporte C; Eric Kandel Institute, Department of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.
  • Pitaval A; Department of Medical Genetics, Life Sciences Institute, University of British Columbia, Vancouver, British Columbia (BC), Canada.
  • Bah TS; Department of Medical Genetics, Life Sciences Institute, University of British Columbia, Vancouver, British Columbia (BC), Canada.
  • Pomeranz G; School of Biomedical Engineering, University of British Columbia, Vancouver, British Columbia (BC), Canada.
  • Bissardon C; Univ. Grenoble Alpes, CEA, IRIG/BGE, BIOMICS, 38000, Grenoble, France.
  • Kaal J; Univ. Grenoble Alpes, CEA, LETI, DTBS, 38000, Grenoble, France.
  • Leopoldi A; Univ. Grenoble Alpes, CEA, IRIG/BGE, BIOMICS, 38000, Grenoble, France.
  • Long DA; Univ. Grenoble Alpes, CEA, IRIG, BGE, Gen&Chem, 38000, Grenoble, France.
  • Blandin P; Developmental Biology and Cancer Programme, UCL Great Ormond Street Institute of Child Health, London, UK.
  • Achard JL; Univ. Grenoble Alpes, CEA, LETI, DTBS, 38000, Grenoble, France.
  • Battail C; Univ. Grenoble Alpes, CEA, LETI, DTBS, 38000, Grenoble, France.
  • Hagelkruys A; Institute of Molecular Biotechnology of the Austrian Academy of Sciences, IMBA, Dr. Bohr-Gasse 3, 1030, Vienna, Austria.
  • Navarro F; Eric Kandel Institute, Department of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.
  • Fouillet Y; Developmental Biology and Cancer Programme, UCL Great Ormond Street Institute of Child Health, London, UK.
  • Penninger JM; Univ. Grenoble Alpes, CEA, LETI, DTBS, 38000, Grenoble, France.
  • Gidrol X; Université Grenoble Alpes, CNRS, Grenoble INP, LEGI, 38000, Grenoble, France.
Nat Commun ; 15(1): 1452, 2024 Feb 16.
Article de En | MEDLINE | ID: mdl-38365780
ABSTRACT
The development of vascular networks in microfluidic chips is crucial for the long-term culture of three-dimensional cell aggregates such as spheroids, organoids, tumoroids, or tissue explants. Despite rapid advancement in microvascular network systems and organoid technologies, vascularizing organoids-on-chips remains a challenge in tissue engineering. Most existing microfluidic devices poorly reflect the complexity of in vivo flows and require complex technical set-ups. Considering these constraints, we develop a platform to establish and monitor the formation of endothelial networks around mesenchymal and pancreatic islet spheroids, as well as blood vessel organoids generated from pluripotent stem cells, cultured for up to 30 days on-chip. We show that these networks establish functional connections with the endothelium-rich spheroids and vascular organoids, as they successfully provide intravascular perfusion to these structures. We find that organoid growth, maturation, and function are enhanced when cultured on-chip using our vascularization method. This microphysiological system represents a viable organ-on-chip model to vascularize diverse biological 3D tissues and sets the stage to establish organoid perfusions using advanced microfluidics.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Ilots pancréatiques / Microfluidique Langue: En Journal: Nat Commun Sujet du journal: BIOLOGIA / CIENCIA Année: 2024 Type de document: Article Pays d'affiliation: France

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Ilots pancréatiques / Microfluidique Langue: En Journal: Nat Commun Sujet du journal: BIOLOGIA / CIENCIA Année: 2024 Type de document: Article Pays d'affiliation: France
...