A microfabricated deformability-based flow cytometer with application to malaria

Malaria resulting from Plasmodium falciparum infection is a major cause of human suffering and mortality. Red blood cell (RBC) deformability plays a major role in the pathogenesis of malaria. Here we introduce an automated microfabricated “deformability cytometer” that measures dynamic mechanical re...

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Main Authors: Bow, Hansen, Pivkin, Igor V., Diez Silva, Monica, Goldfless, Stephen Jacob, Dao, Ming, Niles, Jacquin, Suresh, Subra, Han, Jongyoon
Other Authors: Massachusetts Institute of Technology. Department of Biological Engineering
Format: Article
Language:en_US
Published: Royal Society of Chemistry 2012
Online Access:http://hdl.handle.net/1721.1/73098
https://orcid.org/0000-0002-6223-6831
https://orcid.org/0000-0001-7215-1439
https://orcid.org/0000-0002-6250-8796
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author Bow, Hansen
Pivkin, Igor V.
Diez Silva, Monica
Goldfless, Stephen Jacob
Dao, Ming
Niles, Jacquin
Suresh, Subra
Han, Jongyoon
author2 Massachusetts Institute of Technology. Department of Biological Engineering
author_facet Massachusetts Institute of Technology. Department of Biological Engineering
Bow, Hansen
Pivkin, Igor V.
Diez Silva, Monica
Goldfless, Stephen Jacob
Dao, Ming
Niles, Jacquin
Suresh, Subra
Han, Jongyoon
author_sort Bow, Hansen
collection MIT
description Malaria resulting from Plasmodium falciparum infection is a major cause of human suffering and mortality. Red blood cell (RBC) deformability plays a major role in the pathogenesis of malaria. Here we introduce an automated microfabricated “deformability cytometer” that measures dynamic mechanical responses of 10[superscript 3] to 10[superscript 4] individual RBCs in a cell population. Fluorescence measurements of each RBC are simultaneously acquired, resulting in a population-based correlation between biochemical properties, such as cell surface markers, and dynamic mechanical deformability. This device is especially applicable to heterogeneous cell populations. We demonstrate its ability to mechanically characterize a small number of P. falciparum-infected (ring stage) RBCs in a large population of uninfected RBCs. Furthermore, we are able to infer quantitative mechanical properties of individual RBCs from the observed dynamic behavior through a dissipative particle dynamics (DPD) model. These methods collectively provide a systematic approach to characterize the biomechanical properties of cells in a high-throughput manner.
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spelling mit-1721.1/730982022-10-01T23:01:02Z A microfabricated deformability-based flow cytometer with application to malaria Bow, Hansen Pivkin, Igor V. Diez Silva, Monica Goldfless, Stephen Jacob Dao, Ming Niles, Jacquin Suresh, Subra Han, Jongyoon Massachusetts Institute of Technology. Department of Biological Engineering Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science Massachusetts Institute of Technology. Department of Materials Science and Engineering Bow, Hansen Pivkin, Igor V. Diez Silva, Monica Goldfless, Stephen Jacob Dao, Ming Niles, Jacquin Suresh, Subra Han, Jongyoon Malaria resulting from Plasmodium falciparum infection is a major cause of human suffering and mortality. Red blood cell (RBC) deformability plays a major role in the pathogenesis of malaria. Here we introduce an automated microfabricated “deformability cytometer” that measures dynamic mechanical responses of 10[superscript 3] to 10[superscript 4] individual RBCs in a cell population. Fluorescence measurements of each RBC are simultaneously acquired, resulting in a population-based correlation between biochemical properties, such as cell surface markers, and dynamic mechanical deformability. This device is especially applicable to heterogeneous cell populations. We demonstrate its ability to mechanically characterize a small number of P. falciparum-infected (ring stage) RBCs in a large population of uninfected RBCs. Furthermore, we are able to infer quantitative mechanical properties of individual RBCs from the observed dynamic behavior through a dissipative particle dynamics (DPD) model. These methods collectively provide a systematic approach to characterize the biomechanical properties of cells in a high-throughput manner. National Institutes of Health (U.S.) (Grant R01 HL094270-01A1) National Institutes of Health (U.S.) (Grant 1-R01-GM076689-01) Singapore-MIT Alliance for Research and Technology Center 2012-09-21T16:00:29Z 2012-09-21T16:00:29Z 2011-02 2010-10 Article http://purl.org/eprint/type/JournalArticle 1473-0197 1473-0189 http://hdl.handle.net/1721.1/73098 Bow, Hansen et al. “A Microfabricated Deformability-based Flow Cytometer with Application to Malaria.” Lab on a Chip 11.6 (2011): 1065. https://orcid.org/0000-0002-6223-6831 https://orcid.org/0000-0001-7215-1439 https://orcid.org/0000-0002-6250-8796 en_US http://dx.doi.org/10.1039/c0lc00472c Lab on a Chip Creative Commons Attribution-Noncommercial-Share Alike 3.0 http://creativecommons.org/licenses/by-nc-sa/3.0/ application/pdf Royal Society of Chemistry PubMed Central
spellingShingle Bow, Hansen
Pivkin, Igor V.
Diez Silva, Monica
Goldfless, Stephen Jacob
Dao, Ming
Niles, Jacquin
Suresh, Subra
Han, Jongyoon
A microfabricated deformability-based flow cytometer with application to malaria
title A microfabricated deformability-based flow cytometer with application to malaria
title_full A microfabricated deformability-based flow cytometer with application to malaria
title_fullStr A microfabricated deformability-based flow cytometer with application to malaria
title_full_unstemmed A microfabricated deformability-based flow cytometer with application to malaria
title_short A microfabricated deformability-based flow cytometer with application to malaria
title_sort microfabricated deformability based flow cytometer with application to malaria
url http://hdl.handle.net/1721.1/73098
https://orcid.org/0000-0002-6223-6831
https://orcid.org/0000-0001-7215-1439
https://orcid.org/0000-0002-6250-8796
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