A single-chain derivative of an integrin-activating antibody potentiates organoid growth in Matrigel and collagen hydrogels

Current methods of culturing human epithelial organoids from adult stem cells may not be compatible with clinical applications as they rely on xenogeneic, chemically undefined or non-standardized components such as the basement membrane extract Matrigel. Matrigel provides a source of extracellular matrix molecules, including laminins and collagen IV, which interact with β1 integrins expressed on organoid cells. Here we describe a single-chain (sc) version of antibody TS2/16 that allosterically activates integrin β1 function in organoids. The addition of monomeric scTS2/16 to organoid medium results in up to a fivefold increase in the yield of all gastrointestinal organoids grown in Matrigel. Moreover, scTS2/16 supports a six- to sevenfold increase in the yield of these organoids when cultured in collagen I hydrogels, both in 3D and 2D. Collagen I is well defined, available in clinical-grade formulations and, when combined with scTS2/16, may support the clinical application of epithelial organoids derived from gastrointestinal tissues and other epithelial sources.

Authors

Institutions

Publication Details

Journal
Nature Biotechnology
Published
2025-10-28
DOI
https://doi.org/10.1038/s41587-025-02874-8
Citations
2
Primary Topic
Cell Adhesion Molecules Research
Type
article
Field-Weighted Citation Impact
3.24
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

A single-chain derivative of an integrin-activating antibody potentiates organoid growth in Matrigel and collagen hydrogels

Timothy A. Springer, Johan H. van Es, Claudia Y. Janda, Daniel Krueger et al.
2 citations
Nature Biotechnology
Cell Adhesion Molecules Research
3.24
article

A single-chain derivative of an integrin-activating antibody potentiates organoid growth in Matrigel and collagen hydrogels

Timothy A. Springer, Johan H. van Es, Claudia Y. Janda, Daniel Krueger, Daisong Wang, Arnoud Sonnenberg, Matthijs S. Abendroth, Hans Clevers, Benjamin Chalopin, Gijs J. F. van Son, Emma Bokobza, Robin Schreurs, Joost J.A.P.M. Wijnakker, Wim B. M. de Lau, Fenna L. H. van Rijt
article en
2 citations

Abstract

Current methods of culturing human epithelial organoids from adult stem cells may not be compatible with clinical applications as they rely on xenogeneic, chemically undefined or non-standardized components such as the basement membrane extract Matrigel. Matrigel provides a source of extracellular matrix molecules, including laminins and collagen IV, which interact with β1 integrins expressed on organoid cells. Here we describe a single-chain (sc) version of antibody TS2/16 that allosterically activates integrin β1 function in organoids. The addition of monomeric scTS2/16 to organoid medium results in up to a fivefold increase in the yield of all gastrointestinal organoids grown in Matrigel. Moreover, scTS2/16 supports a six- to sevenfold increase in the yield of these organoids when cultured in collagen I hydrogels, both in 3D and 2D. Collagen I is well defined, available in clinical-grade formulations and, when combined with scTS2/16, may support the clinical application of epithelial organoids derived from gastrointestinal tissues and other epithelial sources.

Nature Biotechnology
Roche (Switzerland) (CH), Boston Children's Hospital (US), Royal Netherlands Academy of Arts and Sciences (NL), Harvard University (US), The Netherlands Cancer Institute (NL), Princess Máxima Center (NL), Lonza (Switzerland) (CH)
Openalex Percentile: Top 8%
Cell Adhesion Molecules Research
3.24
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.