Evidence map›Paper›PMID 31875698›Full record

ArticleAmerican journal of physiology. Cell physiology2020

Bioenergetics underlying single-cell migration on aligned nanofiber scaffolds.

Abinash Padhi, Alexander H Thomson, Justin B Perry, Grace N Davis, Ryan P McMillan, Sandra Loesgen, Elizabeth N Kaweesa, Rakesh Kapania, Amrinder S Nain, David A Brown

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Cell physiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

17 citing papers in PubMed, 24 citations in OpenAlex.

  1. Deep learning reveals how cells pull, buckle, and navigate fibrous environments.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  8. Driving adult tissue repair via re-engagement of a pathway required for fetal healing.Molecular therapy : the journal of the American Society of Gene Therapy · 2023
    Article
  9. Sculpting Rupture-Free Nuclear Shapes in Fibrous Environments.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2022
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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

10 authors at 2 institutions in 1 country.

Abinash PadhiDepartment of Mechanical Engineering, Virginia Tech, Blacksburg, Virginia.
Alexander H ThomsonDepartment of Human Nutrition, Foods, and Exercise, Virginia Tech, Blacksburg, Virginia.
Justin B PerryDepartment of Human Nutrition, Foods, and Exercise, Virginia Tech, Blacksburg, Virginia.
Grace N DavisDepartment of Human Nutrition, Foods, and Exercise, Virginia Tech, Blacksburg, Virginia.
Ryan P McMillanDepartment of Human Nutrition, Foods, and Exercise, Virginia Tech, Blacksburg, Virginia.
Sandra LoesgenDepartment of Chemistry, Oregon State University, Corvallis, Oregon.
Elizabeth N KaweesaDepartment of Chemistry, Oregon State University, Corvallis, Oregon.
Rakesh KapaniaDepartment of Aerospace and Ocean Engineering, Virginia Tech, Blacksburg, Virginia.
Amrinder S NainDepartment of Mechanical Engineering, Virginia Tech, Blacksburg, Virginia.
David A BrownDepartment of Human Nutrition, Foods, and Exercise, Virginia Tech, Blacksburg, Virginia.
Virginia Tech · USOregon State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell migration is centrally involved in a myriad of physiological processes, including morphogenesis, wound healing, tissue repair, and metastatic growth. The bioenergetics that underlie migratory behavior are not fully understood, in part because of variations in cell culture media and utilization of experimental cell culture systems that do not model physiological connective extracellular fibrous networks. In this study, we evaluated the bioenergetics of C2C12 myoblast migration and force production on fibronectin-coated nanofiber scaffolds of controlled diameter and alignment, fabricated using a nonelectrospinning spinneret-based tunable engineered parameters (STEP) platform. The contribution of various metabolic pathways to cellular migration was determined using inhibitors of cellular respiration, ATP synthesis, glycolysis, or glucose uptake. Despite immediate effects on oxygen consumption, mitochondrial inhibition only modestly reduced cell migration velocity, whereas inhibitors of glycolysis and cellular glucose uptake led to striking decreases in migration. The migratory metabolic sensitivity was modifiable based on the substrates present in cell culture media. Cells cultured in galactose (instead of glucose) showed substantial migratory sensitivity to mitochondrial inhibition. We used nanonet force microscopy to determine the bioenergetic factors responsible for single-cell force production and observed that neither mitochondrial nor glycolytic inhibition altered single-cell force production. These data suggest that myoblast migration is heavily reliant on glycolysis in cells grown in conventional media. These studies have wide-ranging implications for the causes, consequences, and putative therapeutic treatments aimed at cellular migration.

Indexed as

NanofibersAnimalsAnthracenesCell MovementCells, CulturedEnergy MetabolismGalactoseGlycolysisMiceAnthracenesGalactosemensacarcinbioenergeticsglycolysismigrationmitochondriasingle cell

Identifiers

PMID31875698
PMCPMC7099521
OpenAlexW2998617141

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.