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OrgaSegment: deep-learning based organoid segmentation to quantify CFTR dependent fluid secretion.

Authors :
Lefferts, Juliet W.
Kroes, Suzanne
Smith, Matthew B.
Niemöller, Paul J.
Nieuwenhuijze, Natascha D. A.
Sonneveld van Kooten, Heleen N.
van der Ent, Cornelis K.
Beekman, Jeffrey M.
van Beuningen, Sam F. B.
Source :
Communications Biology; 3/13/2024, Vol. 7 Issue 1, p1-9, 9p
Publication Year :
2024

Abstract

Epithelial ion and fluid transport studies in patient-derived organoids (PDOs) are increasingly being used for preclinical studies, drug development and precision medicine applications. Epithelial fluid transport properties in PDOs can be measured through visual changes in organoid (lumen) size. Such organoid phenotypes have been highly instrumental for the studying of diseases, including cystic fibrosis (CF), which is characterized by genetic mutations of the CF transmembrane conductance regulator (CFTR) ion channel. Here we present OrgaSegment, a MASK-RCNN based deep-learning segmentation model allowing for the segmentation of individual intestinal PDO structures from bright-field images. OrgaSegment recognizes spherical structures in addition to the oddly-shaped organoids that are a hallmark of CF organoids and can be used in organoid swelling assays, including the new drug-induced swelling assay that we show here. OrgaSegment enabled easy quantification of organoid swelling and could discriminate between organoids with different CFTR mutations, as well as measure responses to CFTR modulating drugs. The easy-to-apply label-free segmentation tool can help to study CFTR-based fluid secretion and possibly other epithelial ion transport mechanisms in organoids. A deep learning model—OrgaSegment—is presented for segmentation of individual intestinal patient-derived organoid structures from bright-field images. This enables quantification of organoid swelling and discrimination between organoids with different levels CFTR function and response to therapy. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
23993642
Volume :
7
Issue :
1
Database :
Complementary Index
Journal :
Communications Biology
Publication Type :
Academic Journal
Accession number :
176032548
Full Text :
https://doi.org/10.1038/s42003-024-05966-4