TY - JOUR
T1 - Culture and analysis of kidney tubuloids and perfused tubuloid cells-on-a-chip
AU - Gijzen, Linda
AU - Yousef Yengej, Fjodor A.
AU - Schutgens, Frans
AU - Vormann, Marianne K.
AU - Ammerlaan, Carola M.E.
AU - Nicolas, Arnaud
AU - Kurek, Dorota
AU - Vulto, Paul
AU - Rookmaaker, Maarten B.
AU - Lanz, Henriette L.
AU - Verhaar, Marianne C.
AU - Clevers, Hans
N1 - Publisher Copyright:
© 2021, The Author(s), under exclusive licence to Springer Nature Limited.
PY - 2021/4
Y1 - 2021/4
N2 - Advanced in vitro kidney models are of great importance to the study of renal physiology and disease. Kidney tubuloids can be established from primary cells derived from adult kidney tissue or urine. Tubuloids are three-dimensional multicellular structures that recapitulate tubular function and have been used to study infectious, malignant, metabolic, and genetic diseases. For tubuloids to more closely represent the in vivo kidney, they can be integrated into an organ-on-a-chip system that has a more physiological tubular architecture and allows flow and interaction with vasculature or epithelial and mesenchymal cells from other organs. Here, we describe a detailed protocol for establishing tubuloid cultures from tissue and urine (1–3 weeks), as well as for generating and characterizing tubuloid cell–derived three-dimensional tubular structures in a perfused microfluidic multi-chip platform (7 d). The combination of the two systems yields a powerful in vitro tool that better recapitulates the complexity of the kidney tubule with donor-specific properties.
AB - Advanced in vitro kidney models are of great importance to the study of renal physiology and disease. Kidney tubuloids can be established from primary cells derived from adult kidney tissue or urine. Tubuloids are three-dimensional multicellular structures that recapitulate tubular function and have been used to study infectious, malignant, metabolic, and genetic diseases. For tubuloids to more closely represent the in vivo kidney, they can be integrated into an organ-on-a-chip system that has a more physiological tubular architecture and allows flow and interaction with vasculature or epithelial and mesenchymal cells from other organs. Here, we describe a detailed protocol for establishing tubuloid cultures from tissue and urine (1–3 weeks), as well as for generating and characterizing tubuloid cell–derived three-dimensional tubular structures in a perfused microfluidic multi-chip platform (7 d). The combination of the two systems yields a powerful in vitro tool that better recapitulates the complexity of the kidney tubule with donor-specific properties.
UR - http://www.scopus.com/inward/record.url?scp=85102210759&partnerID=8YFLogxK
U2 - 10.1038/s41596-020-00479-w
DO - 10.1038/s41596-020-00479-w
M3 - Article
C2 - 33674788
AN - SCOPUS:85102210759
SN - 1754-2189
VL - 16
SP - 2023
EP - 2050
JO - Nature Protocols
JF - Nature Protocols
IS - 4
ER -