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
PY - 2024/12/30
Y1 - 2024/12/30
N2 - Matrigel /BME , a basement membrane-like preparation, supports long-term growth of epithelial 3D organoids from adult stem cells [T. Sato , , 262-265 (2009); T. Sato , , 1762-1772 (2011)]. Here, we show that interaction between Matrigel's major component laminin-111 with epithelial a6ß1-integrin is crucial for this process. The outer membrane protein Invasin of is known to activate multiple integrin-ß1 complexes, including integrin a6ß1. 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 , , 262-265 (2009); T. Sato , , 1762-1772 (2011)]. Here, we show that interaction between Matrigel's major component laminin-111 with epithelial a6ß1-integrin is crucial for this process. The outer membrane protein Invasin of is known to activate multiple integrin-ß1 complexes, including integrin a6ß1. 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 - Invasin
KW - integrin
KW - matrigel
KW - organoid
KW - stem cells
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
SN - 0027-8424
VL - 122
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
M1 - e2420595121
ER -