File:Regulation-of-T-Cell-Motility-In-Vitro-and-In-Vivo-by-LPA-and-LPA2-pone.0101655.s001.ogv
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Regulation-of-T-Cell-Motility-In-Vitro-and-In-Vivo-by-LPA-and-LPA2-pone.0101655.s001.ogv (Ogg Theora video file, length 12 s, 256 × 256 pixels, 200 kbps, file size: 293 KB)
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[edit]DescriptionRegulation-of-T-Cell-Motility-In-Vitro-and-In-Vivo-by-LPA-and-LPA2-pone.0101655.s001.ogv |
English: Lpa2-deficiency results in early defects in T cell migration at the HEV (Supplemental to Figure 5). Representative two-photon microscopic images obtained from the popliteal lymph node of wild-type mice. Wild-type and lpa2−/− CD4+ T cells were labeled with CFSE and CMTMR, respectively and (5–10)×106 cells mixed in a 1∶1 ratio together with Texas Red Dextran were injected into wild-type recipients through the orbital sinus. MP-IVM was performed on a microsurgically exposed popliteal lymph node to visualize T cell motility during extravasation at the HEV. The video shows the first 31 minutes of imaging, which is representative of migration over the course of an hour. |
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Source | Movie S1 from Knowlden S, Capece T, Popovic M, Chapman T, Rezaee F, Kim M, Georas S (2014). "Regulation of T Cell Motility In Vitro and In Vivo by LPA and LPA2". PLOS ONE. DOI:10.1371/journal.pone.0101655. PMID 25003200. PMC: 4086949. | ||
Author | Knowlden S, Capece T, Popovic M, Chapman T, Rezaee F, Kim M, Georas S | ||
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This file is licensed under the Creative Commons Attribution 4.0 International license.
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Date/Time | Thumbnail | Dimensions | User | Comment | |
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current | 01:54, 17 July 2014 | 12 s, 256 × 256 (293 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 | Knowlden S, Capece T, Popovic M, Chapman T, Rezaee F, Kim M, Georas S |
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Usage terms | http://creativecommons.org/licenses/by/4.0/ |
Image title | Lpa2-deficiency results in early defects in T cell migration at the HEV (Supplemental to Figure 5). Representative two-photon microscopic images obtained from the popliteal lymph node of wild-type mice. Wild-type and lpa2−/− CD4+ T cells were labeled with CFSE and CMTMR, respectively and (5–10)×106 cells mixed in a 1∶1 ratio together with Texas Red Dextran were injected into wild-type recipients through the orbital sinus. MP-IVM was performed on a microsurgically exposed popliteal lymph node to visualize T cell motility during extravasation at the HEV. The video shows the first 31 minutes of imaging, which is representative of migration over the course of an hour. |
Software used | Xiph.Org libtheora 1.1 20090822 (Thusnelda) |
Date and time of digitizing | 2014 |