Evidence map›Paper›PMID 33643464›Full record

ArticleCellular and molecular bioengineering2021

3D Microwell Platforms for Control of Single Cell 3D Geometry and Intracellular Organization.

Robin E Wilson, Aleksandra K Denisin, Alexander R Dunn, Beth L Pruitt

Open access · greenAbstract read
In one paragraph

Article in Cellular and molecular bioengineering, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. 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

4 authors at 3 institutions in 1 country.

Robin E WilsonDepartment of Mechanical Engineering, Stanford University, Stanford, CA USA.
Aleksandra K DenisinDepartment of Bioengineering, Stanford University, Stanford, CA USA.
Alexander R DunnDepartment of Chemical Engineering, Stanford University, Stanford, CA USA.
Beth L PruittDepartment of Mechanical Engineering, University of California at Santa Barbara, BioEngineering Building 2002, 494 UCen Rd, Santa Barbara, CA 93106-5170 USA.ORCID 0000-0002-4861-2124
Stanford University · USCardiovascular Institute of the South · USUniversity of California, Santa Barbara · US

Funding

From proteins to cells to tissues: A multi-scale assessment of biomechanical regulation by the myosin molecular motorRM1GM131981 · NIGMS · STANFORD UNIVERSITY · PI BERNSTEIN, DANIEL, MACK, DAVID LEE · 2019 to 2023
$10.3M
Molecular mechanisms underlying force transduction at cellular adhesion complexesR35GM130332 · NIGMS · STANFORD UNIVERSITY · PI Alexander R Dunn · 2019 to 2026
$4.9M
Effect of Microgravity on Drug Responses Using Engineered Heart TissuesUG3TR002588 · NCATS · STANFORD UNIVERSITY · PI PRUITT, BETH L, WU, JOSEPH C. · 2018 to 2019
$1.5M
NCATS NIH HHS UG3 TR002588NIGMS NIH HHS R35 GM130332NIGMS NIH HHS RM1 GM131981
6 · The paper itself

Abstract

introductionCell structure and migration is impacted by the mechanical properties and geometry of the cell adhesive environment. Most studies to date investigating the effects of 3D environments on cells have not controlled geometry at the single-cell level, making it difficult to understand the influence of 3D environmental cues on single cells. Here, we developed microwell platforms to investigate the effects of 2D vs. 3D geometries on single-cell F-actin and nuclear organization.

methodsWe used microfabrication techniques to fabricate three polyacrylamide platforms: 3D microwells with a 3D adhesive environment (

resultsWe tuned the mechanical characteristics of the microfabricated platforms by manipulating the gel formulation. Crosslinker ratio strongly influenced geometric swelling whereas total polymer content primarily affected Young's modulus. When comparing cells in these platforms, we found significant effects on F-actin and nuclear structures. Our analysis showed that a 3D/3D environment was necessary to increase actin and nuclear height. A 3D/2D environment was sufficient to increase actin alignment and nuclear aspect ratio compared to a 2D/2D environment.

conclusionsUsing our novel polyacrylamide platforms, we were able to decouple the effects of 3D confinement and adhesive environment, finding that both influenced actin and nuclear structure.

Indexed as

Cell biomechanicsIntracellular structureMechanobiologyMicrowellPolyacrylamide

Identifiers

PMID33643464
PMCPMC7878614
OpenAlexW3050020305

What OpenQuestion holds

Textmetadata
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.