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Senescence chips for ultrahigh‐throughput isolation and removal of senescent cells

Cellular senescence plays an important role in organismal aging and age‐related diseases. However, it is challenging to isolate low numbers of senescent cells from small volumes of biofluids for downstream analysis. Furthermore, there is no technology that could selectively remove senescent cells in...

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Autores principales: Chen, Yuchao, Mao, Pan, Snijders, Antoine M., Wang, Daojing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5847876/
https://www.ncbi.nlm.nih.gov/pubmed/29336105
http://dx.doi.org/10.1111/acel.12722
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author Chen, Yuchao
Mao, Pan
Snijders, Antoine M.
Wang, Daojing
author_facet Chen, Yuchao
Mao, Pan
Snijders, Antoine M.
Wang, Daojing
author_sort Chen, Yuchao
collection PubMed
description Cellular senescence plays an important role in organismal aging and age‐related diseases. However, it is challenging to isolate low numbers of senescent cells from small volumes of biofluids for downstream analysis. Furthermore, there is no technology that could selectively remove senescent cells in a high‐throughput manner. In this work, we developed a novel microfluidic chip platform, termed senescence chip, for ultrahigh‐throughput isolation and removal of senescent cells. The core component of our senescence chip is a slanted and tunable 3D micropillar array with a variety of shutters in the vertical direction for rapid cell sieving, taking advantage of the characteristic cell size increase during cellular senescence. The 3D configuration achieves high throughput, high recovery rate, and device robustness with minimum clogging. We demonstrated proof‐of‐principle applications in isolation and enumeration of senescent mesenchymal stem cells (MSCs) from undiluted human whole blood, and senescent cells from mouse bone marrow after total body irradiation, with the single‐cell resolution. After scale‐up to a multilayer and multichannel structure, our senescence chip achieved ultrahigh‐throughput removal of senescent cells from human whole blood with an efficiency of over 70% at a flow rate of 300 ml/hr. Sensitivity and specificity of our senescence chips could be augmented with implementation of multiscale size separation, and identification of background white blood cells using their cell surface markers such as CD45. With the advantages of high throughput, robustness, and simplicity, our senescence chips may find wide applications and contribute to diagnosis and therapeutic targeting of cellular senescence.
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spelling pubmed-58478762018-04-01 Senescence chips for ultrahigh‐throughput isolation and removal of senescent cells Chen, Yuchao Mao, Pan Snijders, Antoine M. Wang, Daojing Aging Cell Original Articles Cellular senescence plays an important role in organismal aging and age‐related diseases. However, it is challenging to isolate low numbers of senescent cells from small volumes of biofluids for downstream analysis. Furthermore, there is no technology that could selectively remove senescent cells in a high‐throughput manner. In this work, we developed a novel microfluidic chip platform, termed senescence chip, for ultrahigh‐throughput isolation and removal of senescent cells. The core component of our senescence chip is a slanted and tunable 3D micropillar array with a variety of shutters in the vertical direction for rapid cell sieving, taking advantage of the characteristic cell size increase during cellular senescence. The 3D configuration achieves high throughput, high recovery rate, and device robustness with minimum clogging. We demonstrated proof‐of‐principle applications in isolation and enumeration of senescent mesenchymal stem cells (MSCs) from undiluted human whole blood, and senescent cells from mouse bone marrow after total body irradiation, with the single‐cell resolution. After scale‐up to a multilayer and multichannel structure, our senescence chip achieved ultrahigh‐throughput removal of senescent cells from human whole blood with an efficiency of over 70% at a flow rate of 300 ml/hr. Sensitivity and specificity of our senescence chips could be augmented with implementation of multiscale size separation, and identification of background white blood cells using their cell surface markers such as CD45. With the advantages of high throughput, robustness, and simplicity, our senescence chips may find wide applications and contribute to diagnosis and therapeutic targeting of cellular senescence. John Wiley and Sons Inc. 2018-01-16 2018-04 /pmc/articles/PMC5847876/ /pubmed/29336105 http://dx.doi.org/10.1111/acel.12722 Text en © 2018 The Authors. Aging Cell published by the Anatomical Society and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Chen, Yuchao
Mao, Pan
Snijders, Antoine M.
Wang, Daojing
Senescence chips for ultrahigh‐throughput isolation and removal of senescent cells
title Senescence chips for ultrahigh‐throughput isolation and removal of senescent cells
title_full Senescence chips for ultrahigh‐throughput isolation and removal of senescent cells
title_fullStr Senescence chips for ultrahigh‐throughput isolation and removal of senescent cells
title_full_unstemmed Senescence chips for ultrahigh‐throughput isolation and removal of senescent cells
title_short Senescence chips for ultrahigh‐throughput isolation and removal of senescent cells
title_sort senescence chips for ultrahigh‐throughput isolation and removal of senescent cells
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5847876/
https://www.ncbi.nlm.nih.gov/pubmed/29336105
http://dx.doi.org/10.1111/acel.12722
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