Evidence map›Paper›PMID 32363683›Full record

ArticleJournal of biomedical materials research. Part A2020

Interleukin-4 overexpressing mesenchymal stem cells within gelatin-based microribbon hydrogels enhance bone healing in a murine long bone critical-size defect model.

Masaya Ueno, Chi-Wen Lo, Danial Barati, Bogdan Conrad, Tzuhua Lin, Yusuke Kohno, Takeshi Utsunomiya, Ning Zhang, Masahiro Maruyama, Claire Rhee and 7 more

Abstract read
In one paragraph

Article in Journal of biomedical materials research. Part A, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing 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

31 citing papers in PubMed.

  1. Article
  2. Surgical induction model of femoral defect in Wistar rats for bone repair histology.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas · 2026
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  20. [Research progress on the regulation of macrophage polarization by mechanical stimulation in wound healing].Zhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery · 2022
    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

17 authors.

Masaya UenoDepartment of Orthopaedic Surgery, Stanford University, Stanford, California, USA.ORCID 0000-0002-4121-9127
Chi-Wen LoDepartment of Orthopaedic Surgery, Stanford University, Stanford, California, USA.
Danial BaratiDepartment of Orthopaedic Surgery, Stanford University, Stanford, California, USA.
Bogdan ConradStem Cell Biology and Regenerative Medicine Program, Stanford University, Stanford, California, USA.
Tzuhua LinDepartment of Orthopaedic Surgery, Stanford University, Stanford, California, USA.
Yusuke KohnoDepartment of Orthopaedic Surgery, Stanford University, Stanford, California, USA.ORCID 0000-0003-1821-4560
Takeshi UtsunomiyaDepartment of Orthopaedic Surgery, Stanford University, Stanford, California, USA.
Ning ZhangDepartment of Orthopaedic Surgery, Stanford University, Stanford, California, USA.
Masahiro MaruyamaDepartment of Orthopaedic Surgery, Stanford University, Stanford, California, USA.
Claire RheeDepartment of Orthopaedic Surgery, Stanford University, Stanford, California, USA.
Ejun HuangDepartment of Orthopaedic Surgery, Stanford University, Stanford, California, USA.
Monica Romero-LopezDepartment of Orthopaedic Surgery, Stanford University, Stanford, California, USA.
Xinming TongDepartment of Orthopaedic Surgery, Stanford University, Stanford, California, USA.
Zhenyu YaoDepartment of Orthopaedic Surgery, Stanford University, Stanford, California, USA.
Stefan ZwingenbergerUniversity Center for Orthopaedics and Traumatology, University Hospital Carl Gustav Carus at Technische Universität Dresden, Dresden, Germany.
Fan YangDepartment of Orthopaedic Surgery, Stanford University, Stanford, California, USA.
Stuart B GoodmanDepartment of Orthopaedic Surgery, Stanford University, Stanford, California, USA.

Funding

Microribbon scaffold-mediated Immunomodulation for Cranial Bone RepairR01DE024772 · NIDCR · STANFORD UNIVERSITY · PI YANG, FAN · 2015 to 2025
$4.6M
Wear Particle Disease and NF-kappa B SignalingR01AR063717 · NIAMS · STANFORD UNIVERSITY · PI GOODMAN, STUART B · 2012 to 2021
$3.5M
Sliding hydrogels for accelerating cartilage regenerationR01AR074502 · NIAMS · STANFORD UNIVERSITY · PI YANG, FAN · 2019 to 2023
$2.2M
Tissue Engineering Approaches for Improved Treatment of Early Stage Osteonecrosis of the HipR01AR072613 · NIAMS · STANFORD UNIVERSITY · PI GOODMAN, STUART B, YANG, YUNZHI · 2018 to 2022
$2.2M
Neurophysiology of Weakness and Exercise in Rotator Cuff TendinopathyR01AR063713 · NIAMS · UNIVERSITY OF OREGON · PI KARDUNA, ANDREW ROBERT · 2014 to 2018
$1.7M
Customized MSCs to Enhance Healing of Bone DefectsR01AR073145 · NIAMS · STANFORD UNIVERSITY · PI GOODMAN, STUART B · 2018 to 2021
$1.4M
NIAMS NIH HHS R01 AR063713NIAMS NIH HHS R01 AR063717NIAMS NIH HHS R01 AR072613NIAMS NIH HHS R01 AR073145NIAMS NIH HHS R01 AR074502NIDCR NIH HHS R01 DE024772NIH HHS R01AR063713NIH HHS R01AR074502NIH HHS R01DE024772
6 · The paper itself

Abstract

Mesenchymal stem cell (MSC)-based therapy is a promising strategy for bone repair. Furthermore, the innate immune system, and specifically macrophages, plays a crucial role in the differentiation and activation of MSCs. The anti-inflammatory cytokine Interleukin-4 (IL-4) converts pro-inflammatory M1 macrophages into a tissue regenerative M2 phenotype, which enhances MSC differentiation and function. We developed lentivirus-transduced IL-4 overexpressing MSCs (IL-4 MSCs) that continuously produce IL-4 and polarize macrophages toward an M2 phenotype. In the current study, we investigated the potential of IL-4 MSCs delivered using a macroporous gelatin-based microribbon (μRB) scaffold for healing of critical-size long bone defects in Mice. IL-4 MSCs within μRBs enhanced M2 marker expression without inhibiting M1 marker expression in the early phase, and increased macrophage migration into the scaffold. Six weeks after establishing the bone defect, IL-4 MSCs within μRBs enhanced bone formation and helped bridge the long bone defect. IL-4 MSCs delivered using macroporous μRB scaffold is potentially a valuable strategy for the treatment of critical-size long bone defects.

Indexed as

Mesenchymal Stem Cell TransplantationAnimalsBone and BonesCells, CulturedGelatinHydrogelsInterleukin-4MaleMesenchymal Stem CellsMice, Inbred BALB COsteogenesisTissue ScaffoldsTransduction, GeneticUp-RegulationWound HealingGelatinHydrogelsInterleukin-4cell therapyhydrogelIL-4long bone defectmesenchymal stem cells

Identifiers

PMID32363683
PMCPMC7483618

What OpenQuestion holds

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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.