TY - JOUR
T1 - Integrin-activating Yersinia protein Invasin sustains long-term expansion of primary epithelial cells as 2D organoid sheets
AU - Wijnakker, Joost J A P M
AU - van Son, Gijs J F
AU - Krueger, Daniel
AU - van de Wetering, Willine J
AU - Lopez-Iglesias, Carmen
AU - Schreurs, Robin
AU - van Rijt, Fenna
AU - Lim, Sangho
AU - Lin, Lin
AU - Peters, Peter J
AU - Isberg, Ralph R
AU - Janda, Claudia Y
AU - de Lau, Wim
AU - Clevers, Hans
AU - Janda, Claudia Y.
PY - 2025/1/7
Y1 - 2025/1/7
N2 - Matrigel®/BME®, a basement membrane-like preparation, supports long-term growth of epithelial 3D organoids from adult stem cells [T. Sato et al., Nature 459, 262-265 (2009); T. Sato et al., Gastroenterology 141, 1762-1772 (2011)]. Here, we show that interaction between Matrigel's major component laminin-111 with epithelial α6β1-integrin is crucial for this process. The outer membrane protein Invasin of Yersinia is known to activate multiple integrin-β1 complexes, including integrin α6β1. A C-terminal integrin-binding fragment of Invasin, coated on culture plates, mediated gut epithelial cell adhesion. Addition of organoid growth factors allowed multipassage expansion in 2D. Polarization, junction formation, and generation of enterocytes, goblet cells, Paneth cells, and enteroendocrine cells were stable over time. Sustained expansion of other human, mouse, and even snake epithelia was accomplished under comparable conditions. The 2D "organoid sheet" format holds advantages over the 3D "in gel" format in terms of imaging, accessibility of basal and apical domains, and automation for high-throughput screening. Invasin represents a fully defined, affordable, versatile, and animal-free complement to Matrigel®/BME®.
AB - Matrigel®/BME®, a basement membrane-like preparation, supports long-term growth of epithelial 3D organoids from adult stem cells [T. Sato et al., Nature 459, 262-265 (2009); T. Sato et al., Gastroenterology 141, 1762-1772 (2011)]. Here, we show that interaction between Matrigel's major component laminin-111 with epithelial α6β1-integrin is crucial for this process. The outer membrane protein Invasin of Yersinia is known to activate multiple integrin-β1 complexes, including integrin α6β1. A C-terminal integrin-binding fragment of Invasin, coated on culture plates, mediated gut epithelial cell adhesion. Addition of organoid growth factors allowed multipassage expansion in 2D. Polarization, junction formation, and generation of enterocytes, goblet cells, Paneth cells, and enteroendocrine cells were stable over time. Sustained expansion of other human, mouse, and even snake epithelia was accomplished under comparable conditions. The 2D "organoid sheet" format holds advantages over the 3D "in gel" format in terms of imaging, accessibility of basal and apical domains, and automation for high-throughput screening. Invasin represents a fully defined, affordable, versatile, and animal-free complement to Matrigel®/BME®.
KW - Humans
KW - Animals
KW - Organoids/metabolism
KW - Mice
KW - Epithelial Cells/metabolism
KW - Laminin/metabolism
KW - Adhesins, Bacterial/metabolism
KW - Integrin alpha6beta1/metabolism
KW - Drug Combinations
KW - Proteoglycans/metabolism
KW - Collagen/metabolism
KW - Cell Adhesion
U2 - 10.1073/pnas.2420595121
DO - 10.1073/pnas.2420595121
M3 - Article
C2 - 39793062
SN - 0027-8424
VL - 122
SP - e2420595121
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 1
ER -