Comparative mapping of crawling-cell morphodynamics in deep learning-based feature space.

Navigation of fast migrating cells such as amoeba Dictyostelium and immune cells are tightly associated with their morphologies that range from steady polarized forms that support high directionality to those more complex and variable when making frequent turns. Model simulations are essential for q...

Full description

Bibliographic Details
Main Authors: Daisuke Imoto, Nen Saito, Akihiko Nakajima, Gen Honda, Motohiko Ishida, Toyoko Sugita, Sayaka Ishihara, Koko Katagiri, Chika Okimura, Yoshiaki Iwadate, Satoshi Sawai
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2021-08-01
Series:PLoS Computational Biology
Online Access:https://doi.org/10.1371/journal.pcbi.1009237
id doaj-209d54d962e84374aebd4258c6fc93b1
record_format Article
spelling doaj-209d54d962e84374aebd4258c6fc93b12021-08-17T04:32:22ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582021-08-01178e100923710.1371/journal.pcbi.1009237Comparative mapping of crawling-cell morphodynamics in deep learning-based feature space.Daisuke ImotoNen SaitoAkihiko NakajimaGen HondaMotohiko IshidaToyoko SugitaSayaka IshiharaKoko KatagiriChika OkimuraYoshiaki IwadateSatoshi SawaiNavigation of fast migrating cells such as amoeba Dictyostelium and immune cells are tightly associated with their morphologies that range from steady polarized forms that support high directionality to those more complex and variable when making frequent turns. Model simulations are essential for quantitative understanding of these features and their origins, however systematic comparisons with real data are underdeveloped. Here, by employing deep-learning-based feature extraction combined with phase-field modeling framework, we show that a low dimensional feature space for 2D migrating cell morphologies obtained from the shape stereotype of keratocytes, Dictyostelium and neutrophils can be fully mapped by an interlinked signaling network of cell-polarization and protrusion dynamics. Our analysis links the data-driven shape analysis to the underlying causalities by identifying key parameters critical for migratory morphologies both normal and aberrant under genetic and pharmacological perturbations. The results underscore the importance of deciphering self-organizing states and their interplay when characterizing morphological phenotypes.https://doi.org/10.1371/journal.pcbi.1009237
collection DOAJ
language English
format Article
sources DOAJ
author Daisuke Imoto
Nen Saito
Akihiko Nakajima
Gen Honda
Motohiko Ishida
Toyoko Sugita
Sayaka Ishihara
Koko Katagiri
Chika Okimura
Yoshiaki Iwadate
Satoshi Sawai
spellingShingle Daisuke Imoto
Nen Saito
Akihiko Nakajima
Gen Honda
Motohiko Ishida
Toyoko Sugita
Sayaka Ishihara
Koko Katagiri
Chika Okimura
Yoshiaki Iwadate
Satoshi Sawai
Comparative mapping of crawling-cell morphodynamics in deep learning-based feature space.
PLoS Computational Biology
author_facet Daisuke Imoto
Nen Saito
Akihiko Nakajima
Gen Honda
Motohiko Ishida
Toyoko Sugita
Sayaka Ishihara
Koko Katagiri
Chika Okimura
Yoshiaki Iwadate
Satoshi Sawai
author_sort Daisuke Imoto
title Comparative mapping of crawling-cell morphodynamics in deep learning-based feature space.
title_short Comparative mapping of crawling-cell morphodynamics in deep learning-based feature space.
title_full Comparative mapping of crawling-cell morphodynamics in deep learning-based feature space.
title_fullStr Comparative mapping of crawling-cell morphodynamics in deep learning-based feature space.
title_full_unstemmed Comparative mapping of crawling-cell morphodynamics in deep learning-based feature space.
title_sort comparative mapping of crawling-cell morphodynamics in deep learning-based feature space.
publisher Public Library of Science (PLoS)
series PLoS Computational Biology
issn 1553-734X
1553-7358
publishDate 2021-08-01
description Navigation of fast migrating cells such as amoeba Dictyostelium and immune cells are tightly associated with their morphologies that range from steady polarized forms that support high directionality to those more complex and variable when making frequent turns. Model simulations are essential for quantitative understanding of these features and their origins, however systematic comparisons with real data are underdeveloped. Here, by employing deep-learning-based feature extraction combined with phase-field modeling framework, we show that a low dimensional feature space for 2D migrating cell morphologies obtained from the shape stereotype of keratocytes, Dictyostelium and neutrophils can be fully mapped by an interlinked signaling network of cell-polarization and protrusion dynamics. Our analysis links the data-driven shape analysis to the underlying causalities by identifying key parameters critical for migratory morphologies both normal and aberrant under genetic and pharmacological perturbations. The results underscore the importance of deciphering self-organizing states and their interplay when characterizing morphological phenotypes.
url https://doi.org/10.1371/journal.pcbi.1009237
work_keys_str_mv AT daisukeimoto comparativemappingofcrawlingcellmorphodynamicsindeeplearningbasedfeaturespace
AT nensaito comparativemappingofcrawlingcellmorphodynamicsindeeplearningbasedfeaturespace
AT akihikonakajima comparativemappingofcrawlingcellmorphodynamicsindeeplearningbasedfeaturespace
AT genhonda comparativemappingofcrawlingcellmorphodynamicsindeeplearningbasedfeaturespace
AT motohikoishida comparativemappingofcrawlingcellmorphodynamicsindeeplearningbasedfeaturespace
AT toyokosugita comparativemappingofcrawlingcellmorphodynamicsindeeplearningbasedfeaturespace
AT sayakaishihara comparativemappingofcrawlingcellmorphodynamicsindeeplearningbasedfeaturespace
AT kokokatagiri comparativemappingofcrawlingcellmorphodynamicsindeeplearningbasedfeaturespace
AT chikaokimura comparativemappingofcrawlingcellmorphodynamicsindeeplearningbasedfeaturespace
AT yoshiakiiwadate comparativemappingofcrawlingcellmorphodynamicsindeeplearningbasedfeaturespace
AT satoshisawai comparativemappingofcrawlingcellmorphodynamicsindeeplearningbasedfeaturespace
_version_ 1721205404211347456