File:Calcium-sensing-receptors-signal-constitutive-macropinocytosis-and-facilitate-the-uptake-of-NOD2-ncomms11284-s2.ogv
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[edit]DescriptionCalcium-sensing-receptors-signal-constitutive-macropinocytosis-and-facilitate-the-uptake-of-NOD2-ncomms11284-s2.ogv |
English: Supplementary Movie 1 Persistence of macropinosomes and limited mixing with late endosomal/lysosomal contents during the first 15 minutes after uptake 70 kDa dextran. hMDMs were pulsed with Alexa 647-labeled 10 kDa dextran (0.025 mg/mL) for 1 hour followed by a chase at 37°C to label the late endosomal/lysosomal compartment (cyan, upper panel). The hMDMs were then incubated with rhodamine-labeled 70 kDa dextran (0.025 mg/mL) for 1 min at 37°C, in the presence of M-CSF (200 ng/mL) to label newly formed macropinosomes (red, middle panel). The cells were then washed and imaged on a heated stage acquiring an image every 30 seconds for 15 min. The video is displayed at 7 frames per sec. Scale bar = 10 μm. |
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Source | Video file from Canton J, Schlam D, Breuer C, Gütschow M, Glogauer M, Grinstein S (2016). "Calcium-sensing receptors signal constitutive macropinocytosis and facilitate the uptake of NOD2 ligands in macrophages". Nature Communications. DOI:10.1038/ncomms11284. PMID 27050483. PMC: 4823870. | ||
Author | Canton J, Schlam D, Breuer C, Gütschow M, Glogauer M, Grinstein S | ||
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This file is licensed under the Creative Commons Attribution 4.0 International license.
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current | 10:15, 28 October 2016 | 4.4 s, 508 × 609 (709 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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Short title | Supplementary Movie 1 |
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Author | Canton J, Schlam D, Breuer C, Gütschow M, Glogauer M, Grinstein S |
Usage terms | http://creativecommons.org/licenses/by/4.0/ |
Image title | Persistence of macropinosomes and limited mixing with late endosomal/lysosomal contents during the first 15 minutes after uptake 70 kDa dextran. hMDMs were pulsed with Alexa 647-labeled 10 kDa dextran (0.025 mg/mL) for 1 hour followed by a chase at 37°C to label the late endosomal/lysosomal compartment (cyan, upper panel). The hMDMs were then incubated with rhodamine-labeled 70 kDa dextran (0.025 mg/mL) for 1 min at 37°C, in the presence of M-CSF (200 ng/mL) to label newly formed macropinosomes (red, middle panel). The cells were then washed and imaged on a heated stage acquiring an image every 30 seconds for 15 min. The video is displayed at 7 frames per sec. Scale bar |
Software used | Xiph.Org libtheora 1.1 20090822 (Thusnelda) |
Date and time of digitizing | 2016-04-06 |