File:Neurite growth in a microfluidic device.webm
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Original file (WebM audio/video file, VP9, length 20 s, 1,032 × 1,080 pixels, 9.78 Mbps overall, file size: 23.32 MB)
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Captions
Dorsal root ganglion neurons extend neurites in vitro (time lapse over 48 hours)
Summary[edit]
| Description |
English: Neurons were cultured in a microfluidic channel (left) which was connected to a second channel (right) by narrow tunnels. The cell bodies in the left compartment were larger than the tunnels, but neurites are much smaller. The neurons extended neurites through the ~250 µm-long tunnels in less than 24 h. Here, the cells are dorsal root ganglion neurons. The microfluidic device is made of PDMS using soft lithography, then bonded to a glass substrate. The cells were adherent on the glass substrate. The time-lapse video over 48 hours was captured using differential interference contrast microscopy. Time is indicated as days:hours. |
| Date | |
| Source |
https://www.biorxiv.org/content/10.1101/2023.11.06.565744v2 https://doi.org/10.1039/D3LC00963G |
| Author | Peter D. Jones, Beatriz Molina-Martínez, Anita Niedworok and Paolo Cesare |
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| Date/Time | Thumbnail | Dimensions | User | Comment | |
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| current | 22:11, 21 March 2024 | 20 s, 1,032 × 1,080 (23.32 MB) | P2jones (talk | contribs) | Uploaded a work by Peter D. Jones, Beatriz Molina-Martínez, Anita Niedworok and Paolo Cesare from https://www.biorxiv.org/content/10.1101/2023.11.06.565744v2 https://doi.org/10.1039/D3LC00963G with UploadWizard |
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