Evidence map›Paper›PMID 25263687›Full record

ArticleBiomaterials2014

Micro-scale and meso-scale architectural cues cooperate and compete to direct aligned tissue formation.

Christopher L Gilchrist, David S Ruch, Dianne Little, Farshid Guilak

Abstract read
In one paragraph

Article in Biomaterials, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

30 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  16. TRPV4-mediated calcium signaling in mesenchymal stem cells regulates aligned collagen matrix formation and vinculin tension.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  17. Biomaterials: Foreign Bodies or Tuners for the Immune Response?International journal of molecular sciences · 2019
    Review
  18. Review
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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

4 authors.

Christopher L GilchristDepartment of Orthopaedic Surgery, Duke University Medical Center, Durham, NC 27710, USA.
David S RuchDepartment of Orthopaedic Surgery, Duke University Medical Center, Durham, NC 27710, USA.
Dianne LittleDepartment of Orthopaedic Surgery, Duke University Medical Center, Durham, NC 27710, USA.
Farshid GuilakDepartment of Orthopaedic Surgery, Duke University Medical Center, Durham, NC 27710, USA; Department of Biomedical Engineering, Duke University, Durham, NC 27708, USA. Electronic address: guilak@duke.edu.

Funding

Thermally-Triggered Intra-articular Drug Delivery for OAP01AR050245 · NIAMS · DUKE UNIVERSITY · PI SETTON, LORI A. · 2003 to 2012
$11.5M
VISCOELASTIC PROPERTIES OF NORMAL AND OA CHONDRONSR01AG015768 · NIA · WASHINGTON UNIVERSITY · PI GUILAK, FARSHID · 1998 to 2022
$7.7M
OBESITY, BIOMECHANICS, AND INFLAMMATION IN OSTEOARTHRITISR01AG046927 · NIA · WASHINGTON UNIVERSITY · PI GUILAK, FARSHID · 2013 to 2023
$3.2M
Mechanical and Osmotic Signaling in ChondrocytesR01AR048182 · NIAMS · DUKE UNIVERSITY · PI GUILAK, FARSHID · 2003 to 2013
$3.0M
Intrinsic Repair of the Knee MeniscusR01AR048852 · NIAMS · DUKE UNIVERSITY · PI GUILAK, FARSHID · 2007 to 2011
$1.4M
Aligned Tendon or Ligament Derived Matrix Nanoscaffolds for Rotator Cuff RepairK08AR059784 · NIAMS · DUKE UNIVERSITY · PI LITTLE, DIANNE · 2011 to 2015
$491k
Genome Editing of Stem Cells for Analysis of Osteoarthritis Causal VariantsR21AR065956 · NIAMS · DUKE UNIVERSITY · PI GERSBACH, CHARLES A., GUILAK, FARSHID · 2014 to 2015
$382k
Scaffold Microenvironments for Tendon-to-Bone Tissue EngineeringR03AR065764 · NIAMS · PURDUE UNIVERSITY · PI LITTLE, DIANNE · 2014 to 2016
$236k
Microenvironments for Tendon Tissue EngineeringF32AR065888 · NIAMS · DUKE UNIVERSITY · PI GILCHRIST, CHRISTOPHER LEE · 2014 to 2016
$181k
NIAMS NIH HHS AR059784NIAMS NIH HHS AR065764NIAMS NIH HHS AR065888NIAMS NIH HHS AR48182NIAMS NIH HHS AR48852NIAMS NIH HHS AR50245NIAMS NIH HHS F32 AR065888NIAMS NIH HHS K08 AR059784NIAMS NIH HHS P01 AR050245NIAMS NIH HHS R01 AR048182NIAMS NIH HHS R01 AR048852NIAMS NIH HHS R03 AR065764NIAMS NIH HHS R21 AR065956NIA NIH HHS AG15768NIA NIH HHS AG46927NIA NIH HHS R01 AG015768NIA NIH HHS R01 AG046927
6 · The paper itself

Abstract

Tissue and biomaterial microenvironments provide architectural cues that direct important cell behaviors including cell shape, alignment, migration, and resulting tissue formation. These architectural features may be presented to cells across multiple length scales, from nanometers to millimeters in size. In this study, we examined how architectural cues at two distinctly different length scales, "micro-scale" cues on the order of ∼1-2 μm, and "meso-scale" cues several orders of magnitude larger (>100 μm), interact to direct aligned neo-tissue formation. Utilizing a micro-photopatterning (μPP) model system to precisely arrange cell-adhesive patterns, we examined the effects of substrate architecture at these length scales on human mesenchymal stem cell (hMSC) organization, gene expression, and fibrillar collagen deposition. Both micro- and meso-scale architectures directed cell alignment and resulting tissue organization, and when combined, meso cues could enhance or compete against micro-scale cues. As meso boundary aspect ratios were increased, meso-scale cues overrode micro-scale cues and controlled tissue alignment, with a characteristic critical width (∼500 μm) similar to boundary dimensions that exist in vivo in highly aligned tissues. Meso-scale cues acted via both lateral confinement (in a cell-density-dependent manner) and by permitting end-to-end cell arrangements that yielded greater fibrillar collagen deposition. Despite large differences in fibrillar collagen content and organization between μPP architectural conditions, these changes did not correspond with changes in gene expression of key matrix or tendon-related genes. These findings highlight the complex interplay between geometric cues at multiple length scales and may have implications for tissue engineering strategies, where scaffold designs that incorporate cues at multiple length scales could improve neo-tissue organization and resulting functional outcomes.

Indexed as

Batch Cell Culture TechniquesCell AdhesionCell CommunicationCell MovementCell PolarityCell ProliferationCells, CulturedCellular MicroenvironmentGuided Tissue RegenerationHumansMesenchymal Stem CellsNanostructuresParticle SizeSurface PropertiesTissue EngineeringTissue ScaffoldsActinLigamentMesenchymal stem cellMicropatterningNanotopographyTendon

Identifiers

PMID25263687
PMCPMC4345291

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.