Evidence map›Paper›PMID 34413578›Full record

ArticleJournal of micromechanics and microengineering : structures, devices, and systems2020

MEMS device for applying shear and tension to an epithelium combined with fluorescent live cell imaging.

Miguel A Garcia, Ehsan Sadeghipour, Leeya Engel, W James Nelson, Beth L Pruitt

Open access · greenAbstract read
In one paragraph

Article in Journal of micromechanics and microengineering : structures, devices, and systems, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 41% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Review
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

5 authors at 2 institutions in 1 country.

Miguel A Garcia *Department of Biology, Stanford University, Stanford, CA 94305, United States of America.ORCID 0000-0003-4181-5372
Ehsan Sadeghipour *Department of Mechanical Engineering, Stanford University, Stanford, CA 94305, United States of America.
Leeya EngelDepartment of Mechanical Engineering, Stanford University, Stanford, CA 94305, United States of America.
W James NelsonDepartment of Biology, Stanford University, Stanford, CA 94305, United States of America.
Beth L PruittDepartment of Mechanical Engineering, University of California, Santa Barbara, CA 93106, United States of America.
Stanford University · USUniversity of California, Santa Barbara · US

Funding

Supplement to Enhance Wellness and Resiliency in the Graduate EnvironmentT32GM007276 · NIGMS · STANFORD UNIVERSITY · PI MORRISON, ASHBY J. · 1985 to 2023
$32.9M
Cell-Cell Junctions and Epithelial HomeostasisR35GM118064 · NIGMS · STANFORD UNIVERSITY · PI STEARNS, TIM · 2016 to 2018
$2.6M
NIGMS NIH HHS R35 GM118064NIGMS NIH HHS T32 GM007276
6 · The paper itself

Abstract

Mechanical forces play important roles in the biological function of cells and tissues. While numerous studies have probed the force response of cells and measured cell-generated forces, they have primarily focused on tensile, but not shear forces. Here, we describe the design, fabrication, and application of a silicon micromachined device that is capable of independently applying and sensing both tensile and shear forces in an epithelial cell monolayer. We integrated the device with an upright microscope to enable live cell brightfield and fluorescent imaging of cells over many hours following mechanical perturbation. Using devices of increasing stiffness and the same displacement input, we demonstrate that epithelia exhibit concomitant higher maximum resistive tensile forces and quicker force relaxation. In addition, we characterized the force response of the epithelium to cyclic shear loading. While the maximum resistive forces of epithelia under cyclic shear perturbation remained unchanged between cycles, cyclic loading led to faster relaxation of the resistive forces. The device presented here can be applied to studying the force response of other monolayer-forming cell types and is compatible with pharmacological perturbation of cell structures and functions.

Indexed as

cyclic shear loadingepithelial cell monolayerlive cell imagingmechanobiologyMEMSsheartension

Identifiers

PMID34413578
PMCPMC8372846
OpenAlexW3081337334

What OpenQuestion 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 OpenQuestion graph.