Literature DB >> 31793877

Junction Mapper is a novel computer vision tool to decipher cell-cell contact phenotypes.

Helena Brezovjakova1, Chris Tomlinson2, Noor Mohd Naim1, Pamela Swiatlowska1, Jennifer C Erasmus1, Stephan Huveneers3, Julia Gorelik1, Susann Bruche1, Vania Mm Braga1.   

Abstract

Stable cell-cell contacts underpin tissue architecture and organization. Quantification of junctions of mammalian epithelia requires laborious manual measurements that are a major roadblock for mechanistic studies. We designed Junction Mapper as an open access, semi-automated software that defines the status of adhesiveness via the simultaneous measurement of pre-defined parameters at cell-cell contacts. It identifies contacting interfaces and corners with minimal user input and quantifies length, area and intensity of junction markers. Its ability to measure fragmented junctions is unique. Importantly, junctions that considerably deviate from the contiguous staining and straight contact phenotype seen in epithelia are also successfully quantified (i.e. cardiomyocytes or endothelia). Distinct phenotypes of junction disruption can be clearly differentiated among various oncogenes, depletion of actin regulators or stimulation with other agents. Junction Mapper is thus a powerful, unbiased and highly applicable software for profiling cell-cell adhesion phenotypes and facilitate studies on junction dynamics in health and disease.
© 2019, Brezovjakova et al.

Entities:  

Keywords:  cancer biology; cell biology; cell-cell contacts; computer vision; human; image analysis; junction regulation; software development; tissue cohesion

Mesh:

Substances:

Year:  2019        PMID: 31793877      PMCID: PMC7034980          DOI: 10.7554/eLife.45413

Source DB:  PubMed          Journal:  Elife        ISSN: 2050-084X            Impact factor:   8.713


  46 in total

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Review 5.  Sensing of Cytoskeletal Forces by Asymmetric Adherens Junctions.

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Review 6.  New aspects of pathogenesis of atrial fibrillation: remodelling of intercalated discs.

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8.  PAK is required for the disruption of E-cadherin adhesion by the small GTPase Rac.

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9.  Quantification of dynamic morphological drug responses in 3D organotypic cell cultures by automated image analysis.

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Review 10.  Scanning ion conductance microscopy: a convergent high-resolution technology for multi-parametric analysis of living cardiovascular cells.

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Journal:  J R Soc Interface       Date:  2011-02-16       Impact factor: 4.118

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  3 in total

1.  Rac1-PAK1 regulation of Rab11 cycling promotes junction destabilization.

Authors:  Jennifer C Erasmus; Kasia Smolarczyk; Helena Brezovjakova; Noor F Mohd-Naim; Encarnación Lozano; Karl Matter; Vania M M Braga
Journal:  J Cell Biol       Date:  2021-06-07       Impact factor: 10.539

2.  Intrinsic cell rheology drives junction maturation.

Authors:  K Sri-Ranjan; J L Sanchez-Alonso; P Swiatlowska; S Rothery; P Novak; S Gerlach; D Koeninger; B Hoffmann; R Merkel; M M Stevens; S X Sun; J Gorelik; Vania M M Braga
Journal:  Nat Commun       Date:  2022-08-17       Impact factor: 17.694

3.  Dynamic Python-Based Method Provides Quantitative Analysis of Intercellular Junction Organization During S. pneumoniae Infection of the Respiratory Epithelium.

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Journal:  Front Cell Infect Microbiol       Date:  2022-06-10       Impact factor: 6.073

  3 in total

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