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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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 |
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