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Microphysiological sensing platform for an in-situ detection of tissue-secreted cytokines
Understanding the protein-secretion dynamics from single, specific tissues is critical toward the advancement of disease detection and treatments. However, such secretion dynamics remain difficult to measure in vivo due to the uncontrolled contributions from other tissue populations. Here, we descri...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7453918/ https://www.ncbi.nlm.nih.gov/pubmed/32904308 http://dx.doi.org/10.1016/j.biosx.2019.100025 |
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author | Hernández-Albors, Alejandro Castaño, Albert G. Fernández-Garibay, Xiomara Ortega, María Alejandra Balaguer, Jordina Ramón-Azcón, Javier |
author_facet | Hernández-Albors, Alejandro Castaño, Albert G. Fernández-Garibay, Xiomara Ortega, María Alejandra Balaguer, Jordina Ramón-Azcón, Javier |
author_sort | Hernández-Albors, Alejandro |
collection | PubMed |
description | Understanding the protein-secretion dynamics from single, specific tissues is critical toward the advancement of disease detection and treatments. However, such secretion dynamics remain difficult to measure in vivo due to the uncontrolled contributions from other tissue populations. Here, we describe an integrated platform designed for the reliable, near real-time measurements of cytokines secreted from an in vitro single-tissue model. In our setup, we grow 3D biomimetic tissues to discretize cytokine source, and we separate them from a magnetic microbead-based biosensing system using a Transwell insert. This design integrates physiochemically controlled biological activity, high-sensitivity protein detection (LOD < 20 pg mL(−1)), and rapid protein diffusion to enable non-invasive, near real-time measurements. To showcase the specificity and sensitivity of the system, we use our setup to probe the inflammatory process related to the protein Interleukine 6 (IL-6) and to the Tumor Necrosis Factor (TNF-α). We show that our setup can monitor the time-dependence profile of IL-6 and TNF-α secretion that results from the electrical and chemical stimulation of 3D skeletal muscle tissues. We demonstrate a novel and affordable methodology for discretizing the secretion kinetics of specific tissues for advancing metabolic-disorder studies and drug-screening applications. |
format | Online Article Text |
id | pubmed-7453918 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier B.V |
record_format | MEDLINE/PubMed |
spelling | pubmed-74539182020-09-02 Microphysiological sensing platform for an in-situ detection of tissue-secreted cytokines Hernández-Albors, Alejandro Castaño, Albert G. Fernández-Garibay, Xiomara Ortega, María Alejandra Balaguer, Jordina Ramón-Azcón, Javier Biosens Bioelectron X Article Understanding the protein-secretion dynamics from single, specific tissues is critical toward the advancement of disease detection and treatments. However, such secretion dynamics remain difficult to measure in vivo due to the uncontrolled contributions from other tissue populations. Here, we describe an integrated platform designed for the reliable, near real-time measurements of cytokines secreted from an in vitro single-tissue model. In our setup, we grow 3D biomimetic tissues to discretize cytokine source, and we separate them from a magnetic microbead-based biosensing system using a Transwell insert. This design integrates physiochemically controlled biological activity, high-sensitivity protein detection (LOD < 20 pg mL(−1)), and rapid protein diffusion to enable non-invasive, near real-time measurements. To showcase the specificity and sensitivity of the system, we use our setup to probe the inflammatory process related to the protein Interleukine 6 (IL-6) and to the Tumor Necrosis Factor (TNF-α). We show that our setup can monitor the time-dependence profile of IL-6 and TNF-α secretion that results from the electrical and chemical stimulation of 3D skeletal muscle tissues. We demonstrate a novel and affordable methodology for discretizing the secretion kinetics of specific tissues for advancing metabolic-disorder studies and drug-screening applications. Elsevier B.V 2019-10-01 /pmc/articles/PMC7453918/ /pubmed/32904308 http://dx.doi.org/10.1016/j.biosx.2019.100025 Text en © 2019 The Author(s) http://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 Hernández-Albors, Alejandro Castaño, Albert G. Fernández-Garibay, Xiomara Ortega, María Alejandra Balaguer, Jordina Ramón-Azcón, Javier Microphysiological sensing platform for an in-situ detection of tissue-secreted cytokines |
title | Microphysiological sensing platform for an in-situ detection of tissue-secreted cytokines |
title_full | Microphysiological sensing platform for an in-situ detection of tissue-secreted cytokines |
title_fullStr | Microphysiological sensing platform for an in-situ detection of tissue-secreted cytokines |
title_full_unstemmed | Microphysiological sensing platform for an in-situ detection of tissue-secreted cytokines |
title_short | Microphysiological sensing platform for an in-situ detection of tissue-secreted cytokines |
title_sort | microphysiological sensing platform for an in-situ detection of tissue-secreted cytokines |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7453918/ https://www.ncbi.nlm.nih.gov/pubmed/32904308 http://dx.doi.org/10.1016/j.biosx.2019.100025 |
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