Evidence map›Paper›PMID 24751534›Full record

ArticleActa biomaterialia2014

Degradable hydrogels for spatiotemporal control of mesenchymal stem cells localized at decellularized bone allografts.

Michael D Hoffman, Amy H Van Hove, Danielle S W Benoit

Abstract read
In one paragraph

Article in Acta biomaterialia, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
–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

35 citing papers in PubMed.

  1. Article
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  19. Degradable poly(ethylene glycol) (PEG)-based hydrogels for spatiotemporal control of siRNA/nanoparticle delivery.Journal of controlled release : official journal of the Controlled Release Society · 2018
    Article
  20. Development of controlled drug delivery systems for bone fracture-targeted therapeutic delivery: A review.European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V · 2018
    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

3 authors.

Michael D HoffmanUniversity of Rochester, Department of Biomedical Engineering, University of Rochester, 207 Robert B. Goergen Hall, Box 270168, Rochester, NY 14627-0168, USA; University of Rochester, Department of Orthopaedics and Center for Musculoskeletal Research, University of Rochester Medical Center, 207 Robert B. Goergen Hall, Box 270168, Rochester, NY 14627-0168, USA.
Amy H Van HoveUniversity of Rochester, Department of Biomedical Engineering, University of Rochester, 207 Robert B. Goergen Hall, Box 270168, Rochester, NY 14627-0168, USA.
Danielle S W BenoitUniversity of Rochester, Department of Biomedical Engineering, University of Rochester, 207 Robert B. Goergen Hall, Box 270168, Rochester, NY 14627-0168, USA; University of Rochester, Department of Orthopaedics and Center for Musculoskeletal Research, University of Rochester Medical Center, 207 Robert B. Goergen Hall, Box 270168, Rochester, NY 14627-0168, USA; University of Rochester, Department of Chemical Engineering, University of Rochester, 207 Robert B. Goergen Hall, Box 270168, Rochester, NY 14627-0168, USA. Electronic address: benoit@bme.rochester.edu.

Funding

VISUAL INDICES OF NEUROTOXICITYP30ES001247 · NIEHS · UNIVERSITY OF ROCHESTER · PI Martha Susiarjo · 1985 to 2026
$42.8M
PREPARATION AND DISTRUBUTION OF ADULT STEM CELLS: HUMAN &RODENTP40RR017447 · NCRR · TULANE UNIVERSITY OF LOUISIANA · PI PROCKOP, DARWIN JOHNSON · 2003 to 2011
$8.9M
Tissue Engineering Strategies to Revitalize Bone AllograftsR01AR064200 · NIAMS · UNIVERSITY OF ROCHESTER · PI Danielle S. Benoit · 2013 to 2026
$4.0M
Training in Orthopaedic Researchhttps://apps.era.nih.gov/grantfolder/viewInternalGF.era?applId=8841318&folderId=90T32AR053459 · NIAMS · UNIVERSITY OF ROCHESTER · PI ZUSCIK, MICHAEL J · 2006 to 2017
$3.4M
The University of Rochester Core Center for Musculoskeletal Biology and MedicineP30AR061307 · NIAMS · UNIVERSITY OF ROCHESTER · PI SCHWARZ, EDWARD M. · 2011 to 2015
$3.0M
Molecular Multispectral ImagingS10RR026542 · NCRR · UNIVERSITY OF ROCHESTER · PI AWAD, HANI A · 2010 to 2010
$370k
Olympus NanoZoomer RS Whole Slide Imaging SystemS10RR027340 · NCRR · UNIVERSITY OF ROCHESTER · PI BOYCE, BRENDAN F · 2010 to 2010
$340k
NCRR NIH HHS P40 RR017447NCRR NIH HHS P40-RR017447NCRR NIH HHS S10 RR026542NCRR NIH HHS S10-RR026542-01NCRR NIH HHS S10 RR027340NCRR NIH HHS S10-RR027340-01NIAMS NIH HHS P30 AR061307NIAMS NIH HHS P30-AR061307NIAMS NIH HHS R01 AR064200NIAMS NIH HHS R01-AR064200NIAMS NIH HHS T32 AR053459NIAMS NIH HHS T32-AR053459NIEHS NIH HHS P30 ES001247
6 · The paper itself

Abstract

The transplantation of cells, such as mesenchymal stem cells (MSCs), has numerous applications in the field of regenerative medicine. For cell transplantation strategies to be successful therapeutically, cellular localization and persistence must be controlled to maximize cell-mediated contributions to healing. Herein, we demonstrate that hydrolytic degradation of poly(ethylene glycol) (PEG) hydrogels can be used to spatiotemporally control encapsulated MSC localization to decellularized bone allografts, both in vitro and in vivo. By altering the number of hydrolytically degradable lactide repeat units within PEG-d,l-lactide-methacrylate macromers, a series of hydrogels was synthesized that degraded over ∼1, 2 and 3weeks. MSCs were encapsulated within these hydrogels formed around decellularized bone allografts, and non-invasive, longitudinal fluorescence imaging was used to track cell persistence both in vitro and in vivo. Spatiotemporal localization of MSCs to the exterior of bone allograft surfaces was similar to in vitro hydrogel degradation kinetics despite hydrogel mesh sizes being ∼2-3 orders of magnitude smaller than MSC size throughout the degradation process. Thus, localized, cell-mediated degradation and MSC migration from the hydrogels are suspected, particularly as ∼10% of the total transplanted MSC population was shown to persist in close proximity (within ∼650μm) to grafts 7weeks after complete hydrogel degradation. This work demonstrates the therapeutic utility of PEG-based hydrogels for controlling spatiotemporal cell transplantation for a myriad of regenerative medicine strategies.

Indexed as

Absorbable ImplantsAllograftsAnimalsBiocompatible MaterialsBone TransplantationCell-Free SystemEquipment Failure AnalysisFemoral FracturesHydrogelsMaterials TestingMesenchymal Stem CellsMesenchymal Stem Cell TransplantationMiceMice, Inbred C57BLProsthesis DesignSpatio-Temporal AnalysisBiocompatible MaterialsHydrogelsBone allograftsCell transplantationHydrogelsMesenchymal stem cellsTissue engineering

Identifiers

PMID24751534
PMCPMC4085794

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Registered trials

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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.