Magnetic levitation of single cells
Several cellular events cause permanent or transient changes in inherent magnetic and density properties of cells. Characterizing these changes in cell populations is crucial to understand cellular heterogeneity in cancer, immune response, infectious diseases, drug resistance, and evolution. Althoug...
Ausführliche Beschreibung
Autor*in: |
Ahu Arslan Yildiz [verfasserIn] |
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Format: |
Artikel |
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Sprache: |
Englisch |
Erschienen: |
2015 |
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Rechteinformationen: |
Nutzungsrecht: © COPYRIGHT 2015 National Academy of Sciences |
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Schlagwörter: |
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Übergeordnetes Werk: |
Enthalten in: Proceedings of the National Academy of Sciences of the United States of America - Washington, DC : NAS, 1877, 112(2015), 28, Seite E3661-E3668 |
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Übergeordnetes Werk: |
volume:112 ; year:2015 ; number:28 ; pages:E3661-E3668 |
Links: |
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DOI / URN: |
10.1073/pnas.1509250112 |
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OLC1970276215 |
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520 | |a Several cellular events cause permanent or transient changes in inherent magnetic and density properties of cells. Characterizing these changes in cell populations is crucial to understand cellular heterogeneity in cancer, immune response, infectious diseases, drug resistance, and evolution. Although magnetic levitation has previously been used for macroscale objects, its use in life sciences has been hindered by the inability to levitate microscale objects and by the toxicity of metal salts previously applied for levitation. Here, we use magnetic levitation principles for biological characterization and monitoring of cells and cellular events. We demonstrate that each cell type (i.e., cancer, blood, bacteria, and yeast) has a characteristic levitation profile, which we distinguish at an unprecedented resolution of 1 × 10(-4) g ⋅ mL(-1). We have identified unique differences in levitation and density blueprints between breast, esophageal, colorectal, and nonsmall cell lung cancer cell lines, as well as heterogeneity within these seemingly homogenous cell populations. Furthermore, we demonstrate that changes in cellular density and levitation profiles can be monitored in real time at single-cell resolution, allowing quantification of heterogeneous temporal responses of each cell to environmental stressors. These data establish density as a powerful biomarker for investigating living systems and their responses. Thereby, our method enables rapid, density-based imaging and profiling of single cells with intriguing applications, such as label-free identification and monitoring of heterogeneous biological changes under various physiological conditions, including antibiotic or cancer treatment in personalized medicine. | ||
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650 | 4 | |a Bacteria - cytology | |
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650 | 4 | |a Erythrocytes - cytology | |
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650 | 4 | |a Bacteria - drug effects | |
650 | 4 | |a Magnetic suspension | |
650 | 4 | |a Observations | |
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650 | 4 | |a Biomarkers | |
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650 | 4 | |a Drug resistance | |
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700 | 0 | |a Lars M. Steinmetz |4 oth | |
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700 | 0 | |a Naside Gozde Durmus |4 oth | |
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10.1073/pnas.1509250112 doi PQ20160211 (DE-627)OLC1970276215 (DE-599)GBVOLC1970276215 (PRQ)c2518-82436ced3ed995faeafb7f9e5d70ec8252ada5c82eb627494b45e3aaae852e0c3 (KEY)0583363920150000112002803661magneticlevitationofsinglecells DE-627 ger DE-627 rakwb eng 500 DNB 570 AVZ LING fid BIODIV fid Ahu Arslan Yildiz verfasserin aut Magnetic levitation of single cells 2015 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier Several cellular events cause permanent or transient changes in inherent magnetic and density properties of cells. Characterizing these changes in cell populations is crucial to understand cellular heterogeneity in cancer, immune response, infectious diseases, drug resistance, and evolution. Although magnetic levitation has previously been used for macroscale objects, its use in life sciences has been hindered by the inability to levitate microscale objects and by the toxicity of metal salts previously applied for levitation. Here, we use magnetic levitation principles for biological characterization and monitoring of cells and cellular events. We demonstrate that each cell type (i.e., cancer, blood, bacteria, and yeast) has a characteristic levitation profile, which we distinguish at an unprecedented resolution of 1 × 10(-4) g ⋅ mL(-1). We have identified unique differences in levitation and density blueprints between breast, esophageal, colorectal, and nonsmall cell lung cancer cell lines, as well as heterogeneity within these seemingly homogenous cell populations. Furthermore, we demonstrate that changes in cellular density and levitation profiles can be monitored in real time at single-cell resolution, allowing quantification of heterogeneous temporal responses of each cell to environmental stressors. These data establish density as a powerful biomarker for investigating living systems and their responses. Thereby, our method enables rapid, density-based imaging and profiling of single cells with intriguing applications, such as label-free identification and monitoring of heterogeneous biological changes under various physiological conditions, including antibiotic or cancer treatment in personalized medicine. Nutzungsrecht: © COPYRIGHT 2015 National Academy of Sciences Bacteria - cytology Anti-Infective Agents - pharmacology Erythrocytes - cytology Leukocytes - cytology Yeasts - cytology Yeasts - drug effects Bacteria - drug effects Magnetic suspension Observations Cell interaction Biomarkers Toxicity Life sciences Cells Drug resistance Gizem Calibasi oth Ionita Ghiran oth Utkan Demirci oth Kaushik Sridhar oth Sinan Guven oth Ronald W. Davis oth Lars M. Steinmetz oth H. Cumhur Tekin oth Naside Gozde Durmus oth Enthalten in Proceedings of the National Academy of Sciences of the United States of America Washington, DC : NAS, 1877 112(2015), 28, Seite E3661-E3668 (DE-627)129505269 (DE-600)209104-5 (DE-576)014909189 0027-8424 nnns volume:112 year:2015 number:28 pages:E3661-E3668 http://dx.doi.org/10.1073/pnas.1509250112 Volltext http://www.pnas.org/content/112/28/E3661.abstract http://www.ncbi.nlm.nih.gov/pubmed/26124131 http://search.proquest.com/docview/1697798544 GBV_USEFLAG_A SYSFLAG_A GBV_OLC FID-LING FID-BIODIV SSG-OLC-PHY SSG-OLC-CHE SSG-OLC-MAT SSG-OLC-FOR SSG-OLC-PHA SSG-OLC-DE-84 SSG-OPC-MAT SSG-OPC-FOR GBV_ILN_40 GBV_ILN_59 AR 112 2015 28 E3661-E3668 |
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10.1073/pnas.1509250112 doi PQ20160211 (DE-627)OLC1970276215 (DE-599)GBVOLC1970276215 (PRQ)c2518-82436ced3ed995faeafb7f9e5d70ec8252ada5c82eb627494b45e3aaae852e0c3 (KEY)0583363920150000112002803661magneticlevitationofsinglecells DE-627 ger DE-627 rakwb eng 500 DNB 570 AVZ LING fid BIODIV fid Ahu Arslan Yildiz verfasserin aut Magnetic levitation of single cells 2015 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier Several cellular events cause permanent or transient changes in inherent magnetic and density properties of cells. Characterizing these changes in cell populations is crucial to understand cellular heterogeneity in cancer, immune response, infectious diseases, drug resistance, and evolution. Although magnetic levitation has previously been used for macroscale objects, its use in life sciences has been hindered by the inability to levitate microscale objects and by the toxicity of metal salts previously applied for levitation. Here, we use magnetic levitation principles for biological characterization and monitoring of cells and cellular events. We demonstrate that each cell type (i.e., cancer, blood, bacteria, and yeast) has a characteristic levitation profile, which we distinguish at an unprecedented resolution of 1 × 10(-4) g ⋅ mL(-1). We have identified unique differences in levitation and density blueprints between breast, esophageal, colorectal, and nonsmall cell lung cancer cell lines, as well as heterogeneity within these seemingly homogenous cell populations. Furthermore, we demonstrate that changes in cellular density and levitation profiles can be monitored in real time at single-cell resolution, allowing quantification of heterogeneous temporal responses of each cell to environmental stressors. These data establish density as a powerful biomarker for investigating living systems and their responses. Thereby, our method enables rapid, density-based imaging and profiling of single cells with intriguing applications, such as label-free identification and monitoring of heterogeneous biological changes under various physiological conditions, including antibiotic or cancer treatment in personalized medicine. Nutzungsrecht: © COPYRIGHT 2015 National Academy of Sciences Bacteria - cytology Anti-Infective Agents - pharmacology Erythrocytes - cytology Leukocytes - cytology Yeasts - cytology Yeasts - drug effects Bacteria - drug effects Magnetic suspension Observations Cell interaction Biomarkers Toxicity Life sciences Cells Drug resistance Gizem Calibasi oth Ionita Ghiran oth Utkan Demirci oth Kaushik Sridhar oth Sinan Guven oth Ronald W. Davis oth Lars M. Steinmetz oth H. Cumhur Tekin oth Naside Gozde Durmus oth Enthalten in Proceedings of the National Academy of Sciences of the United States of America Washington, DC : NAS, 1877 112(2015), 28, Seite E3661-E3668 (DE-627)129505269 (DE-600)209104-5 (DE-576)014909189 0027-8424 nnns volume:112 year:2015 number:28 pages:E3661-E3668 http://dx.doi.org/10.1073/pnas.1509250112 Volltext http://www.pnas.org/content/112/28/E3661.abstract http://www.ncbi.nlm.nih.gov/pubmed/26124131 http://search.proquest.com/docview/1697798544 GBV_USEFLAG_A SYSFLAG_A GBV_OLC FID-LING FID-BIODIV SSG-OLC-PHY SSG-OLC-CHE SSG-OLC-MAT SSG-OLC-FOR SSG-OLC-PHA SSG-OLC-DE-84 SSG-OPC-MAT SSG-OPC-FOR GBV_ILN_40 GBV_ILN_59 AR 112 2015 28 E3661-E3668 |
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10.1073/pnas.1509250112 doi PQ20160211 (DE-627)OLC1970276215 (DE-599)GBVOLC1970276215 (PRQ)c2518-82436ced3ed995faeafb7f9e5d70ec8252ada5c82eb627494b45e3aaae852e0c3 (KEY)0583363920150000112002803661magneticlevitationofsinglecells DE-627 ger DE-627 rakwb eng 500 DNB 570 AVZ LING fid BIODIV fid Ahu Arslan Yildiz verfasserin aut Magnetic levitation of single cells 2015 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier Several cellular events cause permanent or transient changes in inherent magnetic and density properties of cells. Characterizing these changes in cell populations is crucial to understand cellular heterogeneity in cancer, immune response, infectious diseases, drug resistance, and evolution. Although magnetic levitation has previously been used for macroscale objects, its use in life sciences has been hindered by the inability to levitate microscale objects and by the toxicity of metal salts previously applied for levitation. Here, we use magnetic levitation principles for biological characterization and monitoring of cells and cellular events. We demonstrate that each cell type (i.e., cancer, blood, bacteria, and yeast) has a characteristic levitation profile, which we distinguish at an unprecedented resolution of 1 × 10(-4) g ⋅ mL(-1). We have identified unique differences in levitation and density blueprints between breast, esophageal, colorectal, and nonsmall cell lung cancer cell lines, as well as heterogeneity within these seemingly homogenous cell populations. Furthermore, we demonstrate that changes in cellular density and levitation profiles can be monitored in real time at single-cell resolution, allowing quantification of heterogeneous temporal responses of each cell to environmental stressors. These data establish density as a powerful biomarker for investigating living systems and their responses. Thereby, our method enables rapid, density-based imaging and profiling of single cells with intriguing applications, such as label-free identification and monitoring of heterogeneous biological changes under various physiological conditions, including antibiotic or cancer treatment in personalized medicine. Nutzungsrecht: © COPYRIGHT 2015 National Academy of Sciences Bacteria - cytology Anti-Infective Agents - pharmacology Erythrocytes - cytology Leukocytes - cytology Yeasts - cytology Yeasts - drug effects Bacteria - drug effects Magnetic suspension Observations Cell interaction Biomarkers Toxicity Life sciences Cells Drug resistance Gizem Calibasi oth Ionita Ghiran oth Utkan Demirci oth Kaushik Sridhar oth Sinan Guven oth Ronald W. Davis oth Lars M. Steinmetz oth H. Cumhur Tekin oth Naside Gozde Durmus oth Enthalten in Proceedings of the National Academy of Sciences of the United States of America Washington, DC : NAS, 1877 112(2015), 28, Seite E3661-E3668 (DE-627)129505269 (DE-600)209104-5 (DE-576)014909189 0027-8424 nnns volume:112 year:2015 number:28 pages:E3661-E3668 http://dx.doi.org/10.1073/pnas.1509250112 Volltext http://www.pnas.org/content/112/28/E3661.abstract http://www.ncbi.nlm.nih.gov/pubmed/26124131 http://search.proquest.com/docview/1697798544 GBV_USEFLAG_A SYSFLAG_A GBV_OLC FID-LING FID-BIODIV SSG-OLC-PHY SSG-OLC-CHE SSG-OLC-MAT SSG-OLC-FOR SSG-OLC-PHA SSG-OLC-DE-84 SSG-OPC-MAT SSG-OPC-FOR GBV_ILN_40 GBV_ILN_59 AR 112 2015 28 E3661-E3668 |
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10.1073/pnas.1509250112 doi PQ20160211 (DE-627)OLC1970276215 (DE-599)GBVOLC1970276215 (PRQ)c2518-82436ced3ed995faeafb7f9e5d70ec8252ada5c82eb627494b45e3aaae852e0c3 (KEY)0583363920150000112002803661magneticlevitationofsinglecells DE-627 ger DE-627 rakwb eng 500 DNB 570 AVZ LING fid BIODIV fid Ahu Arslan Yildiz verfasserin aut Magnetic levitation of single cells 2015 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier Several cellular events cause permanent or transient changes in inherent magnetic and density properties of cells. Characterizing these changes in cell populations is crucial to understand cellular heterogeneity in cancer, immune response, infectious diseases, drug resistance, and evolution. Although magnetic levitation has previously been used for macroscale objects, its use in life sciences has been hindered by the inability to levitate microscale objects and by the toxicity of metal salts previously applied for levitation. Here, we use magnetic levitation principles for biological characterization and monitoring of cells and cellular events. We demonstrate that each cell type (i.e., cancer, blood, bacteria, and yeast) has a characteristic levitation profile, which we distinguish at an unprecedented resolution of 1 × 10(-4) g ⋅ mL(-1). We have identified unique differences in levitation and density blueprints between breast, esophageal, colorectal, and nonsmall cell lung cancer cell lines, as well as heterogeneity within these seemingly homogenous cell populations. Furthermore, we demonstrate that changes in cellular density and levitation profiles can be monitored in real time at single-cell resolution, allowing quantification of heterogeneous temporal responses of each cell to environmental stressors. These data establish density as a powerful biomarker for investigating living systems and their responses. Thereby, our method enables rapid, density-based imaging and profiling of single cells with intriguing applications, such as label-free identification and monitoring of heterogeneous biological changes under various physiological conditions, including antibiotic or cancer treatment in personalized medicine. Nutzungsrecht: © COPYRIGHT 2015 National Academy of Sciences Bacteria - cytology Anti-Infective Agents - pharmacology Erythrocytes - cytology Leukocytes - cytology Yeasts - cytology Yeasts - drug effects Bacteria - drug effects Magnetic suspension Observations Cell interaction Biomarkers Toxicity Life sciences Cells Drug resistance Gizem Calibasi oth Ionita Ghiran oth Utkan Demirci oth Kaushik Sridhar oth Sinan Guven oth Ronald W. Davis oth Lars M. Steinmetz oth H. Cumhur Tekin oth Naside Gozde Durmus oth Enthalten in Proceedings of the National Academy of Sciences of the United States of America Washington, DC : NAS, 1877 112(2015), 28, Seite E3661-E3668 (DE-627)129505269 (DE-600)209104-5 (DE-576)014909189 0027-8424 nnns volume:112 year:2015 number:28 pages:E3661-E3668 http://dx.doi.org/10.1073/pnas.1509250112 Volltext http://www.pnas.org/content/112/28/E3661.abstract http://www.ncbi.nlm.nih.gov/pubmed/26124131 http://search.proquest.com/docview/1697798544 GBV_USEFLAG_A SYSFLAG_A GBV_OLC FID-LING FID-BIODIV SSG-OLC-PHY SSG-OLC-CHE SSG-OLC-MAT SSG-OLC-FOR SSG-OLC-PHA SSG-OLC-DE-84 SSG-OPC-MAT SSG-OPC-FOR GBV_ILN_40 GBV_ILN_59 AR 112 2015 28 E3661-E3668 |
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10.1073/pnas.1509250112 doi PQ20160211 (DE-627)OLC1970276215 (DE-599)GBVOLC1970276215 (PRQ)c2518-82436ced3ed995faeafb7f9e5d70ec8252ada5c82eb627494b45e3aaae852e0c3 (KEY)0583363920150000112002803661magneticlevitationofsinglecells DE-627 ger DE-627 rakwb eng 500 DNB 570 AVZ LING fid BIODIV fid Ahu Arslan Yildiz verfasserin aut Magnetic levitation of single cells 2015 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier Several cellular events cause permanent or transient changes in inherent magnetic and density properties of cells. Characterizing these changes in cell populations is crucial to understand cellular heterogeneity in cancer, immune response, infectious diseases, drug resistance, and evolution. Although magnetic levitation has previously been used for macroscale objects, its use in life sciences has been hindered by the inability to levitate microscale objects and by the toxicity of metal salts previously applied for levitation. Here, we use magnetic levitation principles for biological characterization and monitoring of cells and cellular events. We demonstrate that each cell type (i.e., cancer, blood, bacteria, and yeast) has a characteristic levitation profile, which we distinguish at an unprecedented resolution of 1 × 10(-4) g ⋅ mL(-1). We have identified unique differences in levitation and density blueprints between breast, esophageal, colorectal, and nonsmall cell lung cancer cell lines, as well as heterogeneity within these seemingly homogenous cell populations. Furthermore, we demonstrate that changes in cellular density and levitation profiles can be monitored in real time at single-cell resolution, allowing quantification of heterogeneous temporal responses of each cell to environmental stressors. These data establish density as a powerful biomarker for investigating living systems and their responses. Thereby, our method enables rapid, density-based imaging and profiling of single cells with intriguing applications, such as label-free identification and monitoring of heterogeneous biological changes under various physiological conditions, including antibiotic or cancer treatment in personalized medicine. Nutzungsrecht: © COPYRIGHT 2015 National Academy of Sciences Bacteria - cytology Anti-Infective Agents - pharmacology Erythrocytes - cytology Leukocytes - cytology Yeasts - cytology Yeasts - drug effects Bacteria - drug effects Magnetic suspension Observations Cell interaction Biomarkers Toxicity Life sciences Cells Drug resistance Gizem Calibasi oth Ionita Ghiran oth Utkan Demirci oth Kaushik Sridhar oth Sinan Guven oth Ronald W. Davis oth Lars M. Steinmetz oth H. Cumhur Tekin oth Naside Gozde Durmus oth Enthalten in Proceedings of the National Academy of Sciences of the United States of America Washington, DC : NAS, 1877 112(2015), 28, Seite E3661-E3668 (DE-627)129505269 (DE-600)209104-5 (DE-576)014909189 0027-8424 nnns volume:112 year:2015 number:28 pages:E3661-E3668 http://dx.doi.org/10.1073/pnas.1509250112 Volltext http://www.pnas.org/content/112/28/E3661.abstract http://www.ncbi.nlm.nih.gov/pubmed/26124131 http://search.proquest.com/docview/1697798544 GBV_USEFLAG_A SYSFLAG_A GBV_OLC FID-LING FID-BIODIV SSG-OLC-PHY SSG-OLC-CHE SSG-OLC-MAT SSG-OLC-FOR SSG-OLC-PHA SSG-OLC-DE-84 SSG-OPC-MAT SSG-OPC-FOR GBV_ILN_40 GBV_ILN_59 AR 112 2015 28 E3661-E3668 |
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Ahu Arslan Yildiz @@aut@@ Gizem Calibasi @@oth@@ Ionita Ghiran @@oth@@ Utkan Demirci @@oth@@ Kaushik Sridhar @@oth@@ Sinan Guven @@oth@@ Ronald W. Davis @@oth@@ Lars M. Steinmetz @@oth@@ H. Cumhur Tekin @@oth@@ Naside Gozde Durmus @@oth@@ |
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Several cellular events cause permanent or transient changes in inherent magnetic and density properties of cells. Characterizing these changes in cell populations is crucial to understand cellular heterogeneity in cancer, immune response, infectious diseases, drug resistance, and evolution. Although magnetic levitation has previously been used for macroscale objects, its use in life sciences has been hindered by the inability to levitate microscale objects and by the toxicity of metal salts previously applied for levitation. Here, we use magnetic levitation principles for biological characterization and monitoring of cells and cellular events. We demonstrate that each cell type (i.e., cancer, blood, bacteria, and yeast) has a characteristic levitation profile, which we distinguish at an unprecedented resolution of 1 × 10(-4) g ⋅ mL(-1). We have identified unique differences in levitation and density blueprints between breast, esophageal, colorectal, and nonsmall cell lung cancer cell lines, as well as heterogeneity within these seemingly homogenous cell populations. Furthermore, we demonstrate that changes in cellular density and levitation profiles can be monitored in real time at single-cell resolution, allowing quantification of heterogeneous temporal responses of each cell to environmental stressors. These data establish density as a powerful biomarker for investigating living systems and their responses. Thereby, our method enables rapid, density-based imaging and profiling of single cells with intriguing applications, such as label-free identification and monitoring of heterogeneous biological changes under various physiological conditions, including antibiotic or cancer treatment in personalized medicine. |
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Several cellular events cause permanent or transient changes in inherent magnetic and density properties of cells. Characterizing these changes in cell populations is crucial to understand cellular heterogeneity in cancer, immune response, infectious diseases, drug resistance, and evolution. Although magnetic levitation has previously been used for macroscale objects, its use in life sciences has been hindered by the inability to levitate microscale objects and by the toxicity of metal salts previously applied for levitation. Here, we use magnetic levitation principles for biological characterization and monitoring of cells and cellular events. We demonstrate that each cell type (i.e., cancer, blood, bacteria, and yeast) has a characteristic levitation profile, which we distinguish at an unprecedented resolution of 1 × 10(-4) g ⋅ mL(-1). We have identified unique differences in levitation and density blueprints between breast, esophageal, colorectal, and nonsmall cell lung cancer cell lines, as well as heterogeneity within these seemingly homogenous cell populations. Furthermore, we demonstrate that changes in cellular density and levitation profiles can be monitored in real time at single-cell resolution, allowing quantification of heterogeneous temporal responses of each cell to environmental stressors. These data establish density as a powerful biomarker for investigating living systems and their responses. Thereby, our method enables rapid, density-based imaging and profiling of single cells with intriguing applications, such as label-free identification and monitoring of heterogeneous biological changes under various physiological conditions, including antibiotic or cancer treatment in personalized medicine. |
abstract_unstemmed |
Several cellular events cause permanent or transient changes in inherent magnetic and density properties of cells. Characterizing these changes in cell populations is crucial to understand cellular heterogeneity in cancer, immune response, infectious diseases, drug resistance, and evolution. Although magnetic levitation has previously been used for macroscale objects, its use in life sciences has been hindered by the inability to levitate microscale objects and by the toxicity of metal salts previously applied for levitation. Here, we use magnetic levitation principles for biological characterization and monitoring of cells and cellular events. We demonstrate that each cell type (i.e., cancer, blood, bacteria, and yeast) has a characteristic levitation profile, which we distinguish at an unprecedented resolution of 1 × 10(-4) g ⋅ mL(-1). We have identified unique differences in levitation and density blueprints between breast, esophageal, colorectal, and nonsmall cell lung cancer cell lines, as well as heterogeneity within these seemingly homogenous cell populations. Furthermore, we demonstrate that changes in cellular density and levitation profiles can be monitored in real time at single-cell resolution, allowing quantification of heterogeneous temporal responses of each cell to environmental stressors. These data establish density as a powerful biomarker for investigating living systems and their responses. Thereby, our method enables rapid, density-based imaging and profiling of single cells with intriguing applications, such as label-free identification and monitoring of heterogeneous biological changes under various physiological conditions, including antibiotic or cancer treatment in personalized medicine. |
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Magnetic levitation of single cells |
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http://dx.doi.org/10.1073/pnas.1509250112 http://www.pnas.org/content/112/28/E3661.abstract http://www.ncbi.nlm.nih.gov/pubmed/26124131 http://search.proquest.com/docview/1697798544 |
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Gizem Calibasi Ionita Ghiran Utkan Demirci Kaushik Sridhar Sinan Guven Ronald W. Davis Lars M. Steinmetz H. Cumhur Tekin Naside Gozde Durmus |
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Furthermore, we demonstrate that changes in cellular density and levitation profiles can be monitored in real time at single-cell resolution, allowing quantification of heterogeneous temporal responses of each cell to environmental stressors. These data establish density as a powerful biomarker for investigating living systems and their responses. 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