Evidence map›Paper›PMID 26283165›Full record

ArticleActa biomaterialia2015

Engineered composite fascia for stem cell therapy in tissue repair applications.

Perla Ayala, Jeffrey Caves, Erbin Dai, Layla Siraj, Liying Liu, Ovijit Chaudhuri, Carolyn A Haller, David J Mooney, Elliot L Chaikof

Abstract read
In one paragraph

Article in Acta biomaterialia, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

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

  1. Pooled it
  2. Review
  3. Review
  4. Engineering Functional Rat Ovarian Spheroids Using Granulosa and Theca Cells.Reproductive sciences (Thousand Oaks, Calif.) · 2021
    Article
  5. Review
  6. Biofabrication of thick vascularized neo-pedicle flaps for reconstructive surgery.Translational research : the journal of laboratory and clinical medicine · 2019
    Review
  7. Article
  8. Review
  9. Article
  10. 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

9 authors.

Perla AyalaDepartment of Surgery, Harvard Medical School, Beth Israel Deaconess Medical Center, Boston, MA 02215, USA.
Jeffrey CavesDepartment of Surgery, Harvard Medical School, Beth Israel Deaconess Medical Center, Boston, MA 02215, USA.
Erbin DaiDepartment of Surgery, Harvard Medical School, Beth Israel Deaconess Medical Center, Boston, MA 02215, USA.
Layla SirajDepartment of Surgery, Harvard Medical School, Beth Israel Deaconess Medical Center, Boston, MA 02215, USA.
Liying LiuDepartment of Surgery, Harvard Medical School, Beth Israel Deaconess Medical Center, Boston, MA 02215, USA.
Ovijit ChaudhuriDepartment of Mechanical Engineering, Stanford University, Palo Alto, CA 94305, USA.
Carolyn A HallerDepartment of Surgery, Harvard Medical School, Beth Israel Deaconess Medical Center, Boston, MA 02215, USA.
David J MooneyWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02215, USA; School of Engineering and Applied Sciences, Harvard University, Cambridge, MA 02138, USA.
Elliot L ChaikofDepartment of Surgery, Harvard Medical School, Beth Israel Deaconess Medical Center, Boston, MA 02215, USA; Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02215, USA. Electronic address: echaikof@bidmc.harvard.edu.

Funding

A Bioinspired Small Diameter Vascular ConduitR01HL083867 · NHLBI · EMORY UNIVERSITY · PI CHAIKOF, ELLIOT · 2006 to 2010
$3.8M
Autogeneration of an Artery: A Biomimetric StrategyR01HL060464 · NHLBI · EMORY UNIVERSITY · PI CHAIKOF, ELLIOT · 1998 to 2007
$2.3M
Protein Fibers as Design Elements for Arterial ConduitR01HL071136 · NHLBI · EMORY UNIVERSITY · PI CHAIKOF, ELLIOT · 2002 to 2005
$2.2M
Site-Specific Therapies To Prevent Intimal HyperplasiaR01HL106018 · NHLBI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI CHAIKOF, ELLIOT · 2011 to 2014
$1.6M
NHLBI NIH HHS HL083867NHLBI NIH HHS HL106018NHLBI NIH HHS HL60963NHLBI NIH HHS R01 HL060464NHLBI NIH HHS R01 HL071136NHLBI NIH HHS R01 HL083867NHLBI NIH HHS R01 HL106018
6 · The paper itself

Abstract

A critical challenge in tissue regeneration is to develop constructs that effectively integrate with the host tissue. Here, we describe a composite, laser micromachined, collagen-alginate construct containing human mesenchymal stem cells (hMSCs) for tissue repair applications. Collagen type I was fashioned into laminated collagen sheets to form a mechanically robust fascia that was subsequently laser micropatterned with pores of defined dimension and spatial distribution as a means to modulate mechanical behavior and promote tissue integration. Significantly, laser micromachined patterned constructs displayed both substantially greater compliance and suture retention strength than non-patterned constructs. hMSCs were loaded in an RGD-functionalized alginate gel modified to degrade in vivo. Over a 7 day observation period in vitro, high cell viability was observed with constant levels of VEGF, PDGF-β and MCP-1 protein expression. In a full thickness abdominal wall defect model, the composite construct prevented hernia recurrence in Wistar rats over an 8-week period with de novo tissue and vascular network formation and the absence of adhesions to underlying abdominal viscera. As compared to acellular constructs, constructs containing hMSCs displayed greater integration strength (cell seeded: 0.92 ± 0.19 N/mm vs. acellular: 0.59 ± 0.25 N/mm, p=0.01), increased vascularization (cell seeded: 2.7-2.1/hpf vs. acellular: 1.7-2.1/hpf, p<0.03), and increased infiltration of macrophages (cell seeded: 2021-3630 μm(2)/hpf vs. acellular: 1570-2530 μm(2)/hpf, p<0.05). A decrease in the ratio of M1 macrophages to total macrophages was also observed in hMSC-populated samples. Laser micromachined collagen-alginate composites containing hMSCs can be used to bridge soft tissue defects with the capacity for enhanced tissue repair and integration. STATEMENT OF SIGNIFICANCE: Effective restoration of large soft tissue defects caused by trauma or treatment complications represents a critical challenge in the clinic. In this study, a novel composite construct was engineered and evaluated for stem cell delivery and tissue repair. Laser micromachining was used to fabricate patterned, microporous constructs designed with pores of defined size and distribution as a means to tune mechanical responses, accommodate and protect incorporated cells, and enhance tissue integration. The construct was embedded within an engineered alginate gel containing hMSCs. Upon repair of a full thickness abdominal wall defect in a rat model, the composite construct modulated host innate immunity towards a reparative phenotypic response, promoted neovascularization and associated matrix production, and increased the strength of tissue integration.

Indexed as

Tissue ScaffoldsAlginatesAnimalsBiomimetic MaterialsCollagenEquipment DesignEquipment Failure AnalysisFasciaFemaleGlucuronic AcidGuided Tissue RegenerationHerniaHerniorrhaphyHexuronic AcidsHumansMesenchymal Stem Cell TransplantationAlginatesCollagenGlucuronic AcidHexuronic AcidsAlginateCollagenFull thickness abdominal defectHuman mesenchymal stem cellsImmune responseIntegrationTissue repairVascularization

Identifiers

PMID26283165
PMCPMC4584209

What OpenQuestion holds

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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.