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整合素激活蛋白侵袭素可使原代表皮细胞作为二维类器官片长期扩增。

Integrin-activating protein Invasin sustains long-term expansion of primary epithelial cells as 2D organoid sheets.

作者信息

Wijnakker Joost J A P M, van Son Gijs J F, Krueger Daniel, van de Wetering Willine J, Lopez-Iglesias Carmen, Schreurs Robin, van Rijt Fenna, Lim Sangho, Lin Lin, Peters Peter J, Isberg Ralph R, Janda Claudia Y, de Lau Wim, Clevers Hans

机构信息

Oncode Institute, Hubrecht Institute-Royal Netherlands Academy of Arts and Science, Utrecht 3584 CT, The Netherlands.

University Medical Centre, Utrecht 3584 CT, The Netherlands.

出版信息

Proc Natl Acad Sci U S A. 2025 Jan 7;122(1):e2420595121. doi: 10.1073/pnas.2420595121. Epub 2024 Dec 30.

DOI:10.1073/pnas.2420595121
PMID:39793062
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11725944/
Abstract

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 α6β1-integrin is crucial for this process. The outer membrane protein Invasin of 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.

摘要

基质胶/基底膜提取物(Matrigel/BME)是一种类似基底膜的制剂,可支持成体干细胞来源的上皮3D类器官长期生长[T. 佐藤, ,262 - 265(2009年);T. 佐藤, ,1762 - 1772(2011年)]。在此,我们表明基质胶的主要成分层粘连蛋白-111与上皮α6β1整合素之间的相互作用对这一过程至关重要。已知耶尔森菌的外膜蛋白侵袭素可激活多种整合素-β1复合物,包括整合素α6β1。包被在培养板上的侵袭素C端整合素结合片段介导肠道上皮细胞黏附。添加类器官生长因子可实现二维条件下的多次传代扩增。随着时间推移,极化、连接形成以及肠细胞、杯状细胞、潘氏细胞和肠内分泌细胞的生成保持稳定。在类似条件下实现了其他人类、小鼠甚至蛇类上皮细胞的持续扩增。二维“类器官片”形式在成像、基底和顶端结构域的可及性以及高通量筛选自动化方面比三维“凝胶内”形式具有优势。侵袭素是一种完全明确、价格低廉、用途广泛且无动物成分的基质胶/基底膜提取物替代品。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abe5/11725944/d6ba6a772ab4/pnas.2420595121fig05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abe5/11725944/dca514b0b57d/pnas.2420595121fig01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abe5/11725944/d05e2ce00754/pnas.2420595121fig02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abe5/11725944/ed18fdf122ed/pnas.2420595121fig03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abe5/11725944/3faaa70e6a7b/pnas.2420595121fig04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abe5/11725944/d6ba6a772ab4/pnas.2420595121fig05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abe5/11725944/dca514b0b57d/pnas.2420595121fig01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abe5/11725944/d05e2ce00754/pnas.2420595121fig02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abe5/11725944/ed18fdf122ed/pnas.2420595121fig03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abe5/11725944/3faaa70e6a7b/pnas.2420595121fig04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abe5/11725944/d6ba6a772ab4/pnas.2420595121fig05.jpg

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