Evidence map›Paper›PMID 30077567›Full record

ArticleCytotherapy2018

Transplanted interleukin-4--secreting mesenchymal stromal cells show extended survival and increased bone mineral density in the murine femur.

Tzuhua Lin, Jukka Pajarinen, Yusuke Kohno, Masahiro Maruyama, Monica Romero-Lopez, Jhih-Fong Huang, Karthik Nathan, Tahsin N Khan, Zhenyu Yao, Stuart B Goodman

Abstract read
In one paragraph

Article in Cytotherapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.8field-weighted citation impact, top 6% of its field
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

16 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Therapeutic effects of MSCs, genetically modified MSCs, and NFĸB-inhibitor on chronic inflammatory osteolysis in aged mice.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2023
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  11. Modifying MSC Phenotype to Facilitate Bone Healing: Biological Approaches.Frontiers in bioengineering and biotechnology · 2020
    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

10 authors at 1 institution in 1 country.

Tzuhua LinDepartments of Orthopaedic Surgery, Stanford University, Stanford, California, USA.
Jukka PajarinenDepartments of Orthopaedic Surgery, Stanford University, Stanford, California, USA.
Yusuke KohnoDepartments of Orthopaedic Surgery, Stanford University, Stanford, California, USA.
Masahiro MaruyamaDepartments of Orthopaedic Surgery, Stanford University, Stanford, California, USA.
Monica Romero-LopezDepartments of Orthopaedic Surgery, Stanford University, Stanford, California, USA.
Jhih-Fong HuangDepartments of Orthopaedic Surgery, Stanford University, Stanford, California, USA.
Karthik NathanDepartments of Orthopaedic Surgery, Stanford University, Stanford, California, USA.
Tahsin N KhanDepartments of Orthopaedic Surgery, Stanford University, Stanford, California, USA.
Zhenyu YaoDepartments of Orthopaedic Surgery, Stanford University, Stanford, California, USA.
Stuart B GoodmanDepartments of Orthopaedic Surgery, Stanford University, Stanford, California, USA; Bioengineering, Stanford University, Stanford, California, USA. Electronic address: goodbone@stanford.edu.
Stanford University · US

Funding

Wear Particle Disease and NF-kappa B SignalingR01AR063717 · NIAMS · STANFORD UNIVERSITY · PI GOODMAN, STUART B · 2012 to 2021
$3.5M
Customized MSCs to Enhance Healing of Bone DefectsR01AR073145 · NIAMS · STANFORD UNIVERSITY · PI GOODMAN, STUART B · 2018 to 2021
$1.4M
NIAMS NIH HHS R01 AR063717NIAMS NIH HHS R01 AR073145
6 · The paper itself

Abstract

backgroundMesenchymal stromal cell (MSC)-based therapy has great potential to modulate chronic inflammation and enhance tissue regeneration. Crosstalk between MSC-lineage cells and polarized macrophages is critical for bone formation and remodeling in inflammatory bone diseases. However, the translational application of this interaction is limited by the short-term viability of MSCs after cell transplantation.

methodsThree types of genetically modified (GM) MSCs were created: (1) luciferase-expressing reporter MSCs; (2) MSCs that secrete interleukin (IL)-4 either constitutively; and (3) MSCs that secrete IL-4 as a response to nuclear factor kappa-light-chain-enhancer of activated B cell (NFκB) activation. Cells were injected into the murine distal femoral bone marrow cavity. MSC viability and bone formation were examined in vivo. Cytokine secretion was determined in a femoral explant organ culture model.

resultsThe reporter MSCs survived up to 4 weeks post-implantation. No difference in the number of viable cells was found between high (2.5 × 10 DISCUSSION: Transplanted GM MSCs demonstrated prolonged cell viability when transplanted to a compatible niche within the bone marrow cavity. GM IL-4-secreting MSCs may have great potential to enhance bone regeneration in disorders associated with chronic inflammation.

Indexed as

Bone DensityGraft SurvivalMesenchymal Stem Cell TransplantationAnimalsAnti-Inflammatory AgentsBone RegenerationFemurHEK293 CellsHumansInterleukin-4MaleMesenchymal Stem CellsMiceMice, Inbred BALB COsteogenesisAnti-Inflammatory AgentsInterleukin-4anti-inflammationbone regenerationinterleukin-4mesenchymal stromal cells

Identifiers

PMID30077567
PMCPMC6379084
OpenAlexW2886447448

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.