File:A-Quantitative-Comparison-of-Human-HT-1080-Fibrosarcoma-Cells-and-Primary-Human-Dermal-Fibroblasts-pone.0081689.s012.ogv
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A-Quantitative-Comparison-of-Human-HT-1080-Fibrosarcoma-Cells-and-Primary-Human-Dermal-Fibroblasts-pone.0081689.s012.ogv (Ogg Theora video file, length 4.8 s, 500 × 250 pixels, 458 kbps, file size: 268 KB)
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[edit]DescriptionA-Quantitative-Comparison-of-Human-HT-1080-Fibrosarcoma-Cells-and-Primary-Human-Dermal-Fibroblasts-pone.0081689.s012.ogv |
English: Treatment with matrix metalloproteinase inhibitor (GM6001) blocks migration for HT-1080 fibrosarcoma cells in synthetic ECM. Time-lapse images (15 min / frame) illustrating HT-1080s migrating in synthetic ECM (220 Pa, 1000 μM CRGDS) after treatment with DMSO (control, left) or matrix metalloproteinase (MMP) inhibitor (GM6001, right). Images represent minimum intensity z-projections (middle 500 μm of ~1000 μm thick matrix). HT-1080s are shown for the same time frame used for tracking and quantification of motility. No HT-1080s moved more than one cell length after treatment with MMP-inhibitor, demonstrating that proteolysis is required for migration in synthetic ECM. Time shown in Hr:Min. Scale bar = 100 μm. |
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Source | Movie S1 from Schwartz M, Rogers R, Singh S, Lee J, Loveland S, Koepsel J, Witze E, Montanez-Sauri S, Sung K, Tokuda E, Sharma Y, Everhart L, Nguyen E, Zaman M, Beebe D, Ahn N, Murphy W, Anseth K (2013). "A Quantitative Comparison of Human HT-1080 Fibrosarcoma Cells and Primary Human Dermal Fibroblasts Identifies a 3D Migration Mechanism with Properties Unique to the Transformed Phenotype". PLOS ONE. DOI:10.1371/journal.pone.0081689. PMID 24349113. PMC: 3857815. | ||
Author | Schwartz M, Rogers R, Singh S, Lee J, Loveland S, Koepsel J, Witze E, Montanez-Sauri S, Sung K, Tokuda E, Sharma Y, Everhart L, Nguyen E, Zaman M, Beebe D, Ahn N, Murphy W, Anseth K | ||
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This file is licensed under the Creative Commons Attribution 3.0 Unported license.
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Date/Time | Thumbnail | Dimensions | User | Comment | |
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current | 05:08, 20 December 2013 | 4.8 s, 500 × 250 (268 KB) | Open Access Media Importer Bot (talk | contribs) | Automatically uploaded media file from Open Access source. Please report problems or suggestions here. |
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Author | Schwartz M, Rogers R, Singh S, Lee J, Loveland S, Koepsel J, Witze E, Montanez-Sauri S, Sung K, Tokuda E, Sharma Y, Everhart L, Nguyen E, Zaman M, Beebe D, Ahn N, Murphy W, Anseth K |
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Usage terms | http://creativecommons.org/licenses/by/3.0/ |
Image title | Treatment with matrix metalloproteinase inhibitor (GM6001) blocks migration for HT-1080 fibrosarcoma cells in synthetic ECM. Time-lapse images (15 min / frame) illustrating HT-1080s migrating in synthetic ECM (220 Pa, 1000 ?M CRGDS) after treatment with DMSO (control, left) or matrix metalloproteinase (MMP) inhibitor (GM6001, right). Images represent minimum intensity z-projections (middle 500 ?m of ~1000 ?m thick matrix). HT-1080s are shown for the same time frame used for tracking and quantification of motility. No HT-1080s moved more than one cell length after treatment with MMP-inhibitor, demonstrating that proteolysis is required for migration in synthetic ECM. Time shown in Hr:Min. Scale bar |
Software used | Xiph.Org libtheora 1.1 20090822 (Thusnelda) |
Date and time of digitizing | 2013 |