High-Content Quantification of Single-Cell Immune Dynamics

Cells receive time-varying signals from the environment and generate functional responses by secreting their own signaling molecules. Characterizing dynamic input-output relationships in single cells is crucial for understanding and modeling cellular systems. We developed an automated microfluidic s...

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Main Authors: Michael Junkin, Alicia J. Kaestli, Zhang Cheng, Christian Jordi, Cem Albayrak, Alexander Hoffmann, Savaş Tay
Format: Article
Language:English
Published: Elsevier 2016-04-01
Series:Cell Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2211124716302893
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spelling doaj-619ce72e58da408cb4e9ef3555df91392020-11-25T00:18:32ZengElsevierCell Reports2211-12472016-04-0115241142210.1016/j.celrep.2016.03.033High-Content Quantification of Single-Cell Immune DynamicsMichael Junkin0Alicia J. Kaestli1Zhang Cheng2Christian Jordi3Cem Albayrak4Alexander Hoffmann5Savaş Tay6Department of Biosystems Science and Engineering, ETH Zürich, 4058 Basel, SwitzerlandDepartment of Biosystems Science and Engineering, ETH Zürich, 4058 Basel, SwitzerlandInstitute for Quantitative and Computational Biosciences and Department of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, Los Angeles, CA 90025, USADepartment of Biosystems Science and Engineering, ETH Zürich, 4058 Basel, SwitzerlandDepartment of Biosystems Science and Engineering, ETH Zürich, 4058 Basel, SwitzerlandInstitute for Quantitative and Computational Biosciences and Department of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, Los Angeles, CA 90025, USADepartment of Biosystems Science and Engineering, ETH Zürich, 4058 Basel, SwitzerlandCells receive time-varying signals from the environment and generate functional responses by secreting their own signaling molecules. Characterizing dynamic input-output relationships in single cells is crucial for understanding and modeling cellular systems. We developed an automated microfluidic system that delivers precisely defined dynamical inputs to individual living cells and simultaneously measures key immune parameters dynamically. Our system combines nanoliter immunoassays, microfluidic input generation, and time-lapse microscopy, enabling study of previously untestable aspects of immunity by measuring time-dependent cytokine secretion and transcription factor activity from single cells stimulated with dynamic inflammatory inputs. Employing this system to analyze macrophage signal processing under pathogen inputs, we found that the dynamics of TNF secretion are highly heterogeneous and surprisingly uncorrelated with the dynamics of NF-κB, the transcription factor controlling TNF production. Computational modeling of the LPS/TLR4 pathway shows that post-transcriptional regulation by TRIF is a key determinant of noisy and uncorrelated TNF secretion dynamics in single macrophages.http://www.sciencedirect.com/science/article/pii/S2211124716302893single-cell analysisdynamicscytokineNF-κBmicrofluidicinput
collection DOAJ
language English
format Article
sources DOAJ
author Michael Junkin
Alicia J. Kaestli
Zhang Cheng
Christian Jordi
Cem Albayrak
Alexander Hoffmann
Savaş Tay
spellingShingle Michael Junkin
Alicia J. Kaestli
Zhang Cheng
Christian Jordi
Cem Albayrak
Alexander Hoffmann
Savaş Tay
High-Content Quantification of Single-Cell Immune Dynamics
Cell Reports
single-cell analysis
dynamics
cytokine
NF-κB
microfluidic
input
author_facet Michael Junkin
Alicia J. Kaestli
Zhang Cheng
Christian Jordi
Cem Albayrak
Alexander Hoffmann
Savaş Tay
author_sort Michael Junkin
title High-Content Quantification of Single-Cell Immune Dynamics
title_short High-Content Quantification of Single-Cell Immune Dynamics
title_full High-Content Quantification of Single-Cell Immune Dynamics
title_fullStr High-Content Quantification of Single-Cell Immune Dynamics
title_full_unstemmed High-Content Quantification of Single-Cell Immune Dynamics
title_sort high-content quantification of single-cell immune dynamics
publisher Elsevier
series Cell Reports
issn 2211-1247
publishDate 2016-04-01
description Cells receive time-varying signals from the environment and generate functional responses by secreting their own signaling molecules. Characterizing dynamic input-output relationships in single cells is crucial for understanding and modeling cellular systems. We developed an automated microfluidic system that delivers precisely defined dynamical inputs to individual living cells and simultaneously measures key immune parameters dynamically. Our system combines nanoliter immunoassays, microfluidic input generation, and time-lapse microscopy, enabling study of previously untestable aspects of immunity by measuring time-dependent cytokine secretion and transcription factor activity from single cells stimulated with dynamic inflammatory inputs. Employing this system to analyze macrophage signal processing under pathogen inputs, we found that the dynamics of TNF secretion are highly heterogeneous and surprisingly uncorrelated with the dynamics of NF-κB, the transcription factor controlling TNF production. Computational modeling of the LPS/TLR4 pathway shows that post-transcriptional regulation by TRIF is a key determinant of noisy and uncorrelated TNF secretion dynamics in single macrophages.
topic single-cell analysis
dynamics
cytokine
NF-κB
microfluidic
input
url http://www.sciencedirect.com/science/article/pii/S2211124716302893
work_keys_str_mv AT michaeljunkin highcontentquantificationofsinglecellimmunedynamics
AT aliciajkaestli highcontentquantificationofsinglecellimmunedynamics
AT zhangcheng highcontentquantificationofsinglecellimmunedynamics
AT christianjordi highcontentquantificationofsinglecellimmunedynamics
AT cemalbayrak highcontentquantificationofsinglecellimmunedynamics
AT alexanderhoffmann highcontentquantificationofsinglecellimmunedynamics
AT savastay highcontentquantificationofsinglecellimmunedynamics
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