Evidence map›Paper›PMID 20643054›Full record

ArticleBiophysical journal2010

Bimodal analysis reveals a general scaling law governing nondirected and chemotactic cell motility.

J Scott Gruver, Alka A Potdar, Junhwan Jeon, Jiqing Sai, Bridget Anderson, Donna Webb, Ann Richmond, Vito Quaranta, Peter T Cummings, Chang Y Chung

Open access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 2010. 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
0.5field-weighted citation impact, top 36% 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, 10 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

10 authors at 2 institutions in 1 country.

J Scott GruverDepartment of Pharmacology, Vanderbilt University, Nashville, Tennessee, USA.
Alka A Potdar
Junhwan Jeon
Jiqing Sai
Bridget Anderson
Donna Webb
Ann Richmond
Vito Quaranta
Peter T Cummings
Chang Y Chung
Vanderbilt University · USVanderbilt University Medical Center · US

Funding

TrainingU54CA113007 · NCI · VANDERBILT UNIVERSITY · PI ESTRADA-RODGERS, LOURDES · 2004 to 2014
$19.2M
MELANOMA GROWTH STIMULATORY ACTIVITYR01CA034590 · NCI · VANDERBILT UNIVERSITY · PI RICHMOND, ANN · 1986 to 2017
$5.2M
Spatial Regulation of Cytoskeleton During ChemotaxisR01GM068097 · NIGMS · VANDERBILT UNIVERSITY · PI CHUNG, CHANG Y · 2003 to 2012
$2.7M
BLRD VA IK6 BX005225NCI NIH HHS CA113007NCI NIH HHS R01 CA034590NCI NIH HHS U54 CA113007NIGMS NIH HHS GM68097NIGMS NIH HHS R01 GM068097
6 · The paper itself

Abstract

Cell motility is a fundamental process with relevance to embryonic development, immune response, and metastasis. Cells move either spontaneously, in a nondirected fashion, or in response to chemotactic signals, in a directed fashion. Even though they are often studied separately, both forms of motility share many complex processes at the molecular and subcellular scale, e.g., orchestrated cytoskeletal rearrangements and polarization. In addition, at the cellular level both types of motility include persistent runs interspersed with reorientation pauses. Because there is a great range of variability in motility among different cell types, a key challenge in the field is to integrate these multiscale processes into a coherent framework. We analyzed the motility of Dictyostelium cells with bimodal analysis, a method that compares time spent in persistent versus reorientation mode. Unexpectedly, we found that reorientation time is coupled with persistent time in an inverse correlation and, surprisingly, the inverse correlation holds for both nondirected and chemotactic motility, so that the full range of Dictyostelium motility can be described by a single scaling relationship. Additionally, we found an identical scaling relationship for three human cell lines, indicating that the coupling of reorientation and persistence holds across species and making it possible to describe the complexity of cell motility in a surprisingly general and simple manner. With this new perspective, we analyzed the motility of Dictyostelium mutants, and found four in which the coupling between two modes was altered. Our results point to a fundamental underlying principle, described by a simple scaling law, unifying mechanisms of eukaryotic cell motility at several scales.

Indexed as

ChemotaxisModels, BiologicalCell LineDictyosteliumEukaryotic CellsHumansMutationTime Factors

Identifiers

PMID20643054
PMCPMC2905119
OpenAlexW2068094180

What OpenQuestion holds

Textmetadata
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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.