Enabling peristalsis of human colon tumor organoids on microfluidic chips.
- Publisher:
- IOP Publishing Ltd
- Publication Type:
- Journal Article
- Citation:
- Biofabrication, 2022, 14, (1)
- Issue Date:
- 2022-10-25
Closed Access
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20182876_9926412860005671.pdf | 6.93 MB |
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Full metadata record
Field | Value | Language |
---|---|---|
dc.contributor.author | Fang, G | |
dc.contributor.author |
Lu, H |
|
dc.contributor.author | Al-Nakashli, R | |
dc.contributor.author | Chapman, R | |
dc.contributor.author | Zhang, Y | |
dc.contributor.author | Ju, LA | |
dc.contributor.author |
Lin, G |
|
dc.contributor.author | Stenzel, MH | |
dc.contributor.author |
Jin, D |
|
dc.date.accessioned | 2023-01-31T05:19:29Z | |
dc.date.available | 2021-10-12 | |
dc.date.available | 2023-01-31T05:19:29Z | |
dc.date.issued | 2022-10-25 | |
dc.identifier.citation | Biofabrication, 2022, 14, (1) | |
dc.identifier.issn | 1758-5082 | |
dc.identifier.issn | 1758-5090 | |
dc.identifier.uri | http://hdl.handle.net/10453/165678 | |
dc.description.abstract | Peristalsis in the digestive tract is crucial to maintain physiological functions. It remains challenging to mimic the peristaltic microenvironment in gastrointestinal organoid culture. Here, we present a method to model the peristalsis for human colon tumor organoids on a microfluidic chip. The chip contains hundreds of lateral microwells and a surrounding pressure channel. Human colon tumor organoids growing in the microwell were cyclically contracted by pressure channel, mimicking thein vivomechano-stimulus by intestinal muscles. The chip allows the control of peristalsis amplitude and rhythm and the high throughput culture of organoids simultaneously. By applying 8% amplitude with 8 ∼ 10 times min-1, we observed the enhanced expression of Lgr5 and Ki67. Moreover, ellipticine-loaded polymeric micelles showed reduced uptake in the organoids under peristalsis and resulted in compromised anti-tumor efficacy. The results indicate the importance of mechanical stimuli mimicking the physiological environment when usingin vitromodels to evaluate nanoparticles. This work provides a method for attaining more reliable and representative organoids models in nanomedicine. | |
dc.format | Electronic | |
dc.language | eng | |
dc.publisher | IOP Publishing Ltd | |
dc.relation | http://purl.org/au-research/grants/arc/IH150100028 | |
dc.relation | http://purl.org/au-research/grants/arc/LE180100043 | |
dc.relation | http://purl.org/au-research/grants/nhmrc/1160635 | |
dc.relation.ispartof | Biofabrication | |
dc.relation.isbasedon | 10.1088/1758-5090/ac2ef9 | |
dc.rights | info:eu-repo/semantics/closedAccess | |
dc.subject | 0903 Biomedical Engineering, 1004 Medical Biotechnology, 1099 Other Technology | |
dc.subject.mesh | Colonic Neoplasms | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Lab-On-A-Chip Devices | |
dc.subject.mesh | Microfluidics | |
dc.subject.mesh | Organoids | |
dc.subject.mesh | Peristalsis | |
dc.subject.mesh | Tumor Microenvironment | |
dc.subject.mesh | Colonic Neoplasms | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Lab-On-A-Chip Devices | |
dc.subject.mesh | Microfluidics | |
dc.subject.mesh | Organoids | |
dc.subject.mesh | Peristalsis | |
dc.subject.mesh | Tumor Microenvironment | |
dc.subject.mesh | Organoids | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Colonic Neoplasms | |
dc.subject.mesh | Microfluidics | |
dc.subject.mesh | Peristalsis | |
dc.subject.mesh | Lab-On-A-Chip Devices | |
dc.subject.mesh | Tumor Microenvironment | |
dc.title | Enabling peristalsis of human colon tumor organoids on microfluidic chips. | |
dc.type | Journal Article | |
utslib.citation.volume | 14 | |
utslib.location.activity | England | |
utslib.for | 0903 Biomedical Engineering | |
utslib.for | 1004 Medical Biotechnology | |
utslib.for | 1099 Other Technology | |
pubs.organisational-group | /University of Technology Sydney | |
pubs.organisational-group | /University of Technology Sydney/Faculty of Engineering and Information Technology | |
pubs.organisational-group | /University of Technology Sydney/Faculty of Science | |
pubs.organisational-group | /University of Technology Sydney/Faculty of Science/School of Mathematical and Physical Sciences | |
pubs.organisational-group | /University of Technology Sydney/Faculty of Engineering and Information Technology/School of Biomedical Engineering | |
pubs.organisational-group | /University of Technology Sydney/Strength - IBMD - Initiative for Biomedical Devices | |
utslib.copyright.status | closed_access | * |
pubs.consider-herdc | false | |
dc.date.updated | 2023-01-31T05:19:27Z | |
pubs.issue | 1 | |
pubs.publication-status | Published online | |
pubs.volume | 14 | |
utslib.citation.issue | 1 |
Abstract:
Peristalsis in the digestive tract is crucial to maintain physiological functions. It remains challenging to mimic the peristaltic microenvironment in gastrointestinal organoid culture. Here, we present a method to model the peristalsis for human colon tumor organoids on a microfluidic chip. The chip contains hundreds of lateral microwells and a surrounding pressure channel. Human colon tumor organoids growing in the microwell were cyclically contracted by pressure channel, mimicking thein vivomechano-stimulus by intestinal muscles. The chip allows the control of peristalsis amplitude and rhythm and the high throughput culture of organoids simultaneously. By applying 8% amplitude with 8 ∼ 10 times min-1, we observed the enhanced expression of Lgr5 and Ki67. Moreover, ellipticine-loaded polymeric micelles showed reduced uptake in the organoids under peristalsis and resulted in compromised anti-tumor efficacy. The results indicate the importance of mechanical stimuli mimicking the physiological environment when usingin vitromodels to evaluate nanoparticles. This work provides a method for attaining more reliable and representative organoids models in nanomedicine.
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