Evidence map›Paper›PMID 35008089›Full record

ArticleCells, tissues, organs2023

Rapid Prototypable Biomimetic Peristalsis Bioreactor Capable of Concurrent Shear and Multi-Axial Strain.

Abigail J Clevenger, Logan Z Crawford, Dillon Noltensmeyer, Hamed Babaei, Samuel B Mabbott, Reza Avazmohammadi, Shreya Raghavan

Open access · bronzeAbstract read
In one paragraph

Article in Cells, tissues, organs, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.5field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 7 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Abigail J ClevengerDepartment of Biomedical Engineering, Texas A&M University, College Station, Texas, USA.
Logan Z CrawfordDepartment of Biomedical Engineering, Texas A&M University, College Station, Texas, USA.
Dillon NoltensmeyerDepartment of Biomedical Engineering, Texas A&M University, College Station, Texas, USA.
Hamed BabaeiDepartment of Biomedical Engineering, Texas A&M University, College Station, Texas, USA.
Samuel B MabbottDepartment of Biomedical Engineering, Texas A&M University, College Station, Texas, USA.
Reza AvazmohammadiDepartment of Biomedical Engineering, Texas A&M University, College Station, Texas, USA.
Shreya RaghavanDepartment of Biomedical Engineering, Texas A&M University, College Station, Texas, USA.
Texas A&M University · USHouston Methodist · USTexas A&M University System · US

Funding

The effect of systemic hypertension on prognosis of myocardial infarction: Understanding, prediction and therapy evaluationR00HL138288 · NHLBI · TEXAS ENGINEERING EXPERIMENT STATION · PI AVAZMOHAMMADI, REZA · 2020 to 2022
$727k
NHLBI NIH HHS R00 HL138288
6 · The paper itself

Abstract

Peristalsis is a nuanced mechanical stimulus comprised of multi-axial strain (radial and axial strain) and shear stress. Forces associated with peristalsis regulate diverse biological functions including digestion, reproductive function, and urine dynamics. Given the central role peristalsis plays in physiology and pathophysiology, we were motivated to design a bioreactor capable of holistically mimicking peristalsis. We engineered a novel rotating screw-drive based design combined with a peristaltic pump, in order to deliver multi-axial strain and concurrent shear stress to a biocompatible polydimethylsiloxane (PDMS) membrane "wall." Radial indentation and rotation of the screw drive against the wall demonstrated multi-axial strain evaluated via finite element modeling. Experimental measurements of strain using piezoelectric strain resistors were in close alignment with model-predicted values (15.9 ± 4.2% vs. 15.2% predicted). Modeling of shear stress on the "wall" indicated a uniform velocity profile and a moderate shear stress of 0.4 Pa. Human mesenchymal stem cells (hMSCs) seeded on the PDMS "wall" and stimulated with peristalsis demonstrated dramatic changes in actin filament alignment, proliferation, and nuclear morphology compared to static controls, perfusion, or strain, indicating that hMSCs sensed and responded to peristalsis uniquely. Lastly, significant differences were observed in gene expression patterns of calponin, caldesmon, smooth muscle actin, and transgelin, corroborating the propensity of hMSCs toward myogenic differentiation in response to peristalsis. Collectively, our data suggest that the peristalsis bioreactor is capable of generating concurrent multi-axial strain and shear stress on a "wall." hMSCs experience peristalsis differently than perfusion or strain, resulting in changes in proliferation, actin fiber organization, smooth muscle actin expression, and genetic markers of differentiation. The peristalsis bioreactor device has broad utility in the study of development and disease in several organ systems.

Indexed as

BiomimeticsPeristalsisActinsBioreactorsCell DifferentiationHumansActinsBioreactorHuman mesenchymal stem cellsPeristalsis

Identifiers

PMID35008089
PMCPMC9271135
OpenAlexW4206041469

What Socratic holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.