Evidence map›Paper›PMID 30641263›Full record

ArticleBiomaterials2019

Injectable mineralized microsphere-loaded composite hydrogels for bone repair in a sheep bone defect model.

Ganesh C Ingavle, Marissa Gionet-Gonzales, Charlotte E Vorwald, Laurie K Bohannon, Kaitlin Clark, Larry D Galuppo, J Kent Leach

Abstract read
In one paragraph

Article in Biomaterials, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing 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

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

  1. Pooled it
  2. ROS-responsive HBioactive materials · 2027
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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

7 authors.

Ganesh C IngavleDepartment of Biomedical Engineering, University of California, Davis, Davis, CA 95616, USA; Symbiosis Center for Stem Cell Research, Symbiosis International University, Pune 412115, India.
Marissa Gionet-GonzalesDepartment of Biomedical Engineering, University of California, Davis, Davis, CA 95616, USA.
Charlotte E VorwaldDepartment of Biomedical Engineering, University of California, Davis, Davis, CA 95616, USA.
Laurie K BohannonDepartment of Surgical & Radiological Sciences, UC Davis School of Veterinary Medicine, Davis, CA 95616, USA.
Kaitlin ClarkDepartment of Surgical & Radiological Sciences, UC Davis School of Veterinary Medicine, Davis, CA 95616, USA.
Larry D GaluppoDepartment of Surgical & Radiological Sciences, UC Davis School of Veterinary Medicine, Davis, CA 95616, USA.
J Kent LeachDepartment of Biomedical Engineering, University of California, Davis, Davis, CA 95616, USA; Department of Orthopaedic Surgery, School of Medicine, UC Davis Health, Sacramento, CA 95817, USA. Electronic address: jkleach@ucdavis.edu.

Funding

Training Program In Basic & Translational Cardiovascular ScienceT32HL086350 · NHLBI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Martin Cadeiras, David A. Liem · 2008 to 2026
$7.1M
Dual peptide presentation from bioengineered carriers to potentiate stromal cell function and tissue repairR01DE025899 · NIDCR · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LEACH, J. KENT · 2017 to 2021
$2.5M
Biomaterial regulation of cell spheroids to synergistically enhance bone healingR01DE025475 · NIDCR · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LEACH, J. KENT · 2015 to 2019
$1.9M
NHLBI NIH HHS T32 HL086350NIDCR NIH HHS R01 DE025475NIDCR NIH HHS R01 DE025899
6 · The paper itself

Abstract

The efficacy of cell-based therapies as an alternative to autologous bone grafts requires biomaterials to localize cells at the defect and drive osteogenic differentiation. Hydrogels are ideal cell delivery vehicles that can provide instructional cues via their composition or mechanical properties but commonly lack osteoconductive components that nucleate mineral. To address this challenge, we entrapped mesenchymal stromal cells (MSCs) in a composite hydrogel based on two naturally-derived polymers (alginate and hyaluronate) containing biomineralized polymeric microspheres. Mechanical properties of the hydrogels were dependent upon composition. The presentation of the adhesive tripeptide Arginine-Glycine-Aspartic Acid (RGD) from both polymers induced greater osteogenic differentiation of ovine MSCs in vitro compared to gels formed of RGD-alginate or RGD-alginate/hyaluronate alone. We then evaluated the capacity of this construct to stimulate bone healing when transplanting autologous, culture-expanded MSCs into a surgical induced, critical-sized ovine iliac crest bone defect. At 12 weeks post-implantation, defects treated with MSCs transplanted in composite gels exhibited significant increases in blood vessel density, osteoid formation, and bone formation compared to acellular gels or untreated defects. These findings demonstrate the capacity of osteoconductive hydrogels to promote bone formation with autologous MSCs in a large animal bone defect model and provide a promising vehicle for cell-based therapies of bone healing.

Indexed as

AlginatesAnimalsBiocompatible MaterialsBone and BonesHyaluronic AcidHydrogelsInjectionsMesenchymal Stem CellsMesenchymal Stem Cell TransplantationOligopeptidesOsteogenesisSheepAlginatesarginyl-glycyl-aspartic acidBiocompatible Materialshyaluronate alginateHyaluronic AcidHydrogelsOligopeptidesAlginateBiomineralizationHyaluronateHydrogelOsteoconductiveOsteogenesis

Identifiers

PMID30641263
PMCPMC6363840

What OpenQuestion holds

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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.