Publication: Rocker or pump? Transcriptomic response of endothelial cells exposed to peristaltic pump-based unidirectional flow vs. rocker-induced bidirectional flow
cris.virtual.author-orcid | 0000-0002-0905-6399 | |
cris.virtual.author-orcid | 0000-0003-1103-9712 | |
cris.virtualsource.author-orcid | c7faa7e6-bd8f-471c-9819-520bc4335c94 | |
cris.virtualsource.author-orcid | 55b2e20d-cddd-47a5-9ea4-4fadaf2279b1 | |
cris.virtualsource.author-orcid | a093c8e2-2915-4719-a03e-dd3e7a0586d8 | |
cris.virtualsource.author-orcid | 79bc2168-817a-44ea-be31-b11af4269ff4 | |
cris.virtualsource.author-orcid | 0deca364-5c2f-4c14-8b5c-8952ac805d1b | |
datacite.rights | open.access | |
dc.contributor.author | Vahdani, Negar | |
dc.contributor.author | Arora, Prateek | |
dc.contributor.author | van Os, Lisette | |
dc.contributor.author | Ackermann, Denise | |
dc.contributor.author | Mercader, Nadia | |
dc.contributor.author | Guenat, Olivier T. | |
dc.date.accessioned | 2025-08-04T06:32:06Z | |
dc.date.available | 2025-08-04T06:32:06Z | |
dc.date.issued | 2025 | |
dc.description.abstract | Rocking-platform perfusion systems rely on hydrostatic pressure differences to perfuse cells in organ-on-chip devices. These systems are popular due to their tubing-free design, which facilitates parallelization, an essential feature for drug discovery, precision medicine, and academic research. However, most of these systems generate bidirectional flow, which does not accurately replicate the physiological conditions experienced by endothelial cells (ECs) in the microvasculature. To address this limitation, pump-based systems are often employed to generate unidirectional flow, though they require external tubing, thereby limiting scalability compared to rocking platforms. In this study, under matched average flow rates, we compared the transcriptomic responses of endothelial cells exposed to flow generated either by a rocking platform or a peristaltic pump. Our results revealed distinct transcriptomic profiles induced by the two flow modalities, with hundreds of genes differentially expressed between the two conditions. After 4 hours of flow exposure, we observed an enrichment in signaling pathways including NF-κB, ERK, BMP and MAPK. Furthermore, after 24 hours of flow exposure, we identified significant changes in the genes involved in biological processes such as immune cell migration, angiogenesis and vascular and extracellular matrix remodeling, highlighting how different flow generated by a pump or a rocker can shape endothelial cell behavior at the molecular level. | |
dc.description.sponsorship | Graduate School for Cellular and Biomedical Sciences (GCB) | |
dc.description.sponsorship | Multidisciplinary Center for Infectious Diseases (MCID) | |
dc.description.sponsorship | Institute of Anatomy, Developmental Biology and Regeneration | |
dc.description.sponsorship | ARTORG Center for Biomedical Engineering Research | |
dc.description.sponsorship | Institute of Anatomy | |
dc.description.sponsorship | ARTORG Center - Organs-on-Chip Technologies (OOC) | |
dc.identifier.doi | 10.48620/90491 | |
dc.identifier.pmid | 40746301 | |
dc.identifier.publisherDOI | 10.1039/D5LC00553A | |
dc.identifier.uri | https://boris-portal.unibe.ch/handle/20.500.12422/214456 | |
dc.language.iso | en | |
dc.publisher | Royal Society of Chemistry | |
dc.relation.ispartof | Lab on a Chip | |
dc.relation.issn | 1473-0197 | |
dc.relation.issn | 1473-0189 | |
dc.subject | unidirectional flow | |
dc.subject | bidirectional flow | |
dc.subject | shear stress | |
dc.subject | transcriptomics | |
dc.subject | rocker | |
dc.subject | endothelial cells | |
dc.subject | organs-on-chip | |
dc.subject | pulsatile flow | |
dc.subject.ddc | 600 - Technology::620 - Engineering | |
dc.subject.ddc | 500 - Science::570 - Life sciences; biology | |
dc.subject.ddc | 600 - Technology::610 - Medicine & health | |
dc.title | Rocker or pump? Transcriptomic response of endothelial cells exposed to peristaltic pump-based unidirectional flow vs. rocker-induced bidirectional flow | |
dc.type | article | |
dspace.entity.type | Publication | |
dspace.file.type | text | |
oairecerif.author.affiliation | ARTORG Center for Biomedical Engineering Research | |
oairecerif.author.affiliation | Institute of Anatomy | |
oairecerif.author.affiliation | ARTORG Center - Organs-on-Chip Technologies (OOC) | |
oairecerif.author.affiliation | Institute of Anatomy, Developmental Biology and Regeneration | |
oairecerif.author.affiliation | ARTORG Center - Organs-on-Chip Technologies (OOC) | |
oairecerif.author.affiliation2 | Graduate School for Cellular and Biomedical Sciences (GCB) | |
oairecerif.author.affiliation2 | Institute of Anatomy, Developmental Biology and Regeneration | |
oairecerif.author.affiliation2 | Institute of Anatomy | |
oairecerif.author.affiliation2 | ARTORG Center for Biomedical Engineering Research | |
oairecerif.author.affiliation3 | Multidisciplinary Center for Infectious Diseases (MCID) | |
oairecerif.author.affiliation3 | ARTORG Center - Organs-on-Chip Technologies (OOC) | |
unibe.additional.sponsorship | Graduate School for Cellular and Biomedical Sciences (GCB) | |
unibe.additional.sponsorship | Multidisciplinary Center for Infectious Diseases (MCID) | |
unibe.additional.sponsorship | Institute of Anatomy, Developmental Biology and Regeneration | |
unibe.contributor.orcid | 0000-0002-0905-6399 | |
unibe.contributor.orcid | 0000-0003-1103-9712 | |
unibe.contributor.role | author | |
unibe.contributor.role | author | |
unibe.contributor.role | author | |
unibe.contributor.role | author | |
unibe.contributor.role | author | |
unibe.contributor.role | corresponding author | |
unibe.description.ispublished | inpress | |
unibe.refereed | true | |
unibe.subtype.article | journal |
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