Evidence map›Paper›PMID 18620486›Full record

ArticleTissue engineering. Part A2008

A neural network model for cell classification based on single-cell biomechanical properties.

Eric M Darling, Farshid Guilak

Open access · greenAbstract read
In one paragraph

Article in Tissue engineering. Part A, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

10 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. High-Throughput Assessment of Cellular Mechanical Properties.Annual review of biomedical engineering · 2015
    Review
  7. Article
  8. Article
  9. Cellular mechanical properties reflect the differentiation potential of adipose-derived mesenchymal stem cells.Proceedings of the National Academy of Sciences of the United States of America · 2012
    Article
  10. Article
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

2 authors at 1 institution in 1 country.

Eric M DarlingDepartment of Surgery, Duke University Medical Center, Durham, North Carolina, USA.
Farshid Guilak
Duke Medical Center · US

Funding

Pilot Project for the DTMI CRA ProgramUL1RR024128 · NCRR · DUKE UNIVERSITY · PI CALIFF, ROBERT M · 2006 to 2010
$48.1M
Thermally-Triggered Intra-articular Drug Delivery for OAP01AR050245 · NIAMS · DUKE UNIVERSITY · PI KRAUS, VIRGINIA · 2003 to 2012
$11.5M
VISCOELASTIC PROPERTIES OF NORMAL AND OA CHONDRONSR01AG015768 · NIA · WASHINGTON UNIVERSITY · PI GUILAK, FARSHID · 1998 to 2022
$7.7M
Mechanical and Osmotic Signaling in ChondrocytesR01AR048182 · NIAMS · DUKE UNIVERSITY · PI GUILAK, FARSHID · 2003 to 2013
$3.0M
Training in Biomolecular and Tissue EngineeringT32EB001630 · NIBIB · DUKE UNIVERSITY · PI GUILAK, FARSHID · 2003 to 2007
$1.7M
Intrinsic Repair of the Knee MeniscusR01AR048852 · NIAMS · DUKE UNIVERSITY · PI GUILAK, FARSHID · 2007 to 2011
$1.4M
Adult Stem Cell Enrichment via Biomechanical CharacterizationR00AR054673 · NIAMS · BROWN UNIVERSITY · PI DARLING, ERIC M · 2009 to 2011
$829k
Adult Stem Cell Enrichment via Biomechanical CharacterizationK99AR054673 · NIAMS · DUKE UNIVERSITY · PI DARLING, ERIC M · 2007 to 2007
$81k
Stem cell characterization using atomic force microscopyF32AR053448 · NIAMS · DUKE UNIVERSITY · PI DARLING, ERIC M · 2006 to 2006
$49k
NCRR NIH HHS RR024128NCRR NIH HHS UL1 RR024128NIAMS NIH HHS AR48182NIAMS NIH HHS AR48852NIAMS NIH HHS AR50245NIAMS NIH HHS AR53448NIAMS NIH HHS AR54673NIAMS NIH HHS F32 AR053448NIAMS NIH HHS K99 AR054673NIAMS NIH HHS P01 AR050245NIAMS NIH HHS R00 AR054673NIAMS NIH HHS R01 AR048182NIAMS NIH HHS R01 AR048852NIA NIH HHS AG15768NIA NIH HHS R01 AG015768NIBIB NIH HHS T32 EB001630
6 · The paper itself

Abstract

The potential success of tissue engineering or other cell-based therapies is dependent on factors such as the purity and homogeneity of the source cell populations. The ability to enrich cell harvests for specific phenotypes can have significant effects on the overall success of such therapies. While most techniques for cell sorting or enrichment have relied on cell surface markers, recent studies have shown that single-cell mechanical properties can serve as identifying markers of phenotype. In this study, a neural network modeling approach was developed to classify mesenchymal-derived primary and stem cells based on their biomechanical properties. Cell sorting was simulated using previously published data characterizing the mechanical properties of several different cell types as measured by atomic force microscopy. Neural networks were trained using combined data sets, with the resultant groupings analyzed for their purity, efficiency, and enrichment. Heterogeneous populations of zonal chondrocytes, chondrosarcoma cells, and mesenchymal-lineage cells, respectively, could all be classified into enriched subpopulations. Additionally, adult stem cells (adipose-derived or bone marrow-derived) separated disproportionately into nodes associated with the three primary mesenchymal lineages examined. These findings suggest that mathematical approaches such as neural network modeling, in combination with novel measures of cell properties, may provide a means of classifying and eventually sorting mixed populations of cells that are otherwise difficult to identify using more established techniques. In this respect, the identification of biomechanically based cell properties that increase the percentage of stem cells capable of differentiating into predictable lineages may improve the overall success of cell-based therapies.

Indexed as

Models, BiologicalNeural Networks, ComputerAnimalsBiomechanical PhenomenaCell SeparationEukaryotic CellsHumans

Identifiers

PMID18620486
PMCPMC2748927
OpenAlexW1985380531

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.