Cargando…

C-MORE: A high-content single-cell morphology recognition methodology for liquid biopsies toward personalized cardiovascular medicine

Cellular morphology has the capacity to serve as a surrogate for cellular state and functionality. However, primary cardiomyocytes, the standard model in cardiovascular research, are highly heterogeneous cells and therefore impose methodological challenges to analysis. Hence, we aimed to devise a ro...

Descripción completa

Detalles Bibliográficos
Autores principales: Furkel, Jennifer, Knoll, Maximilian, Din, Shabana, Bogert, Nicolai V., Seeger, Timon, Frey, Norbert, Abdollahi, Amir, Katus, Hugo A., Konstandin, Mathias H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8606902/
https://www.ncbi.nlm.nih.gov/pubmed/34841289
http://dx.doi.org/10.1016/j.xcrm.2021.100436
_version_ 1784602437702647808
author Furkel, Jennifer
Knoll, Maximilian
Din, Shabana
Bogert, Nicolai V.
Seeger, Timon
Frey, Norbert
Abdollahi, Amir
Katus, Hugo A.
Konstandin, Mathias H.
author_facet Furkel, Jennifer
Knoll, Maximilian
Din, Shabana
Bogert, Nicolai V.
Seeger, Timon
Frey, Norbert
Abdollahi, Amir
Katus, Hugo A.
Konstandin, Mathias H.
author_sort Furkel, Jennifer
collection PubMed
description Cellular morphology has the capacity to serve as a surrogate for cellular state and functionality. However, primary cardiomyocytes, the standard model in cardiovascular research, are highly heterogeneous cells and therefore impose methodological challenges to analysis. Hence, we aimed to devise a robust methodology to deconvolute cardiomyocyte morphology on a single-cell level: C-MORE (cellular morphology recognition) is a workflow from bench to data analysis tailored for heterogeneous primary cells using our R package cmoRe. We demonstrate its utility in proof-of-principle applications such as modulation of canonical hypertrophy pathways and linkage of genotype-phenotype in human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs). In our pilot study, exposure of cardiomyocytes to blood plasma prior to versus after aortic valve replacement allows identification of a disease fingerprint and reflects partial reversibility following therapeutic intervention. C-MORE is a valuable tool for cardiovascular research with possible fields of application in basic research and personalized medicine.
format Online
Article
Text
id pubmed-8606902
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-86069022021-11-26 C-MORE: A high-content single-cell morphology recognition methodology for liquid biopsies toward personalized cardiovascular medicine Furkel, Jennifer Knoll, Maximilian Din, Shabana Bogert, Nicolai V. Seeger, Timon Frey, Norbert Abdollahi, Amir Katus, Hugo A. Konstandin, Mathias H. Cell Rep Med Article Cellular morphology has the capacity to serve as a surrogate for cellular state and functionality. However, primary cardiomyocytes, the standard model in cardiovascular research, are highly heterogeneous cells and therefore impose methodological challenges to analysis. Hence, we aimed to devise a robust methodology to deconvolute cardiomyocyte morphology on a single-cell level: C-MORE (cellular morphology recognition) is a workflow from bench to data analysis tailored for heterogeneous primary cells using our R package cmoRe. We demonstrate its utility in proof-of-principle applications such as modulation of canonical hypertrophy pathways and linkage of genotype-phenotype in human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs). In our pilot study, exposure of cardiomyocytes to blood plasma prior to versus after aortic valve replacement allows identification of a disease fingerprint and reflects partial reversibility following therapeutic intervention. C-MORE is a valuable tool for cardiovascular research with possible fields of application in basic research and personalized medicine. Elsevier 2021-11-03 /pmc/articles/PMC8606902/ /pubmed/34841289 http://dx.doi.org/10.1016/j.xcrm.2021.100436 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Furkel, Jennifer
Knoll, Maximilian
Din, Shabana
Bogert, Nicolai V.
Seeger, Timon
Frey, Norbert
Abdollahi, Amir
Katus, Hugo A.
Konstandin, Mathias H.
C-MORE: A high-content single-cell morphology recognition methodology for liquid biopsies toward personalized cardiovascular medicine
title C-MORE: A high-content single-cell morphology recognition methodology for liquid biopsies toward personalized cardiovascular medicine
title_full C-MORE: A high-content single-cell morphology recognition methodology for liquid biopsies toward personalized cardiovascular medicine
title_fullStr C-MORE: A high-content single-cell morphology recognition methodology for liquid biopsies toward personalized cardiovascular medicine
title_full_unstemmed C-MORE: A high-content single-cell morphology recognition methodology for liquid biopsies toward personalized cardiovascular medicine
title_short C-MORE: A high-content single-cell morphology recognition methodology for liquid biopsies toward personalized cardiovascular medicine
title_sort c-more: a high-content single-cell morphology recognition methodology for liquid biopsies toward personalized cardiovascular medicine
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8606902/
https://www.ncbi.nlm.nih.gov/pubmed/34841289
http://dx.doi.org/10.1016/j.xcrm.2021.100436
work_keys_str_mv AT furkeljennifer cmoreahighcontentsinglecellmorphologyrecognitionmethodologyforliquidbiopsiestowardpersonalizedcardiovascularmedicine
AT knollmaximilian cmoreahighcontentsinglecellmorphologyrecognitionmethodologyforliquidbiopsiestowardpersonalizedcardiovascularmedicine
AT dinshabana cmoreahighcontentsinglecellmorphologyrecognitionmethodologyforliquidbiopsiestowardpersonalizedcardiovascularmedicine
AT bogertnicolaiv cmoreahighcontentsinglecellmorphologyrecognitionmethodologyforliquidbiopsiestowardpersonalizedcardiovascularmedicine
AT seegertimon cmoreahighcontentsinglecellmorphologyrecognitionmethodologyforliquidbiopsiestowardpersonalizedcardiovascularmedicine
AT freynorbert cmoreahighcontentsinglecellmorphologyrecognitionmethodologyforliquidbiopsiestowardpersonalizedcardiovascularmedicine
AT abdollahiamir cmoreahighcontentsinglecellmorphologyrecognitionmethodologyforliquidbiopsiestowardpersonalizedcardiovascularmedicine
AT katushugoa cmoreahighcontentsinglecellmorphologyrecognitionmethodologyforliquidbiopsiestowardpersonalizedcardiovascularmedicine
AT konstandinmathiash cmoreahighcontentsinglecellmorphologyrecognitionmethodologyforliquidbiopsiestowardpersonalizedcardiovascularmedicine