Evidence map›Paper›PMID 21499838›Full record

ArticlePharmaceutical research2011

Mesenchymal stem cells as a gene delivery vehicle for successful islet transplantation.

Hao Wu, Wenli Lu, Ram I Mahato

Abstract read
In one paragraph

Article in Pharmaceutical research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

13 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
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  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Mesenchymal stem cells in tissue repair.Frontiers in immunology · 2013
    Review
  10. Third-party mesenchymal stem cells improved human islet transplantation in a humanized diabetic mouse model.Molecular therapy : the journal of the American Society of Gene Therapy · 2013
    Article
  11. Mesenchymal stem cell-based therapy.Molecular pharmaceutics · 2013
    Review
  12. Article
  13. 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 at 1 institution in 1 country.

Hao WuDepartment of Pharmaceutical Sciences, University of Tennessee Health Science Center, 19 S. Manassas, RM 224, Memphis, Tennessee 38103-3308, USA.
Wenli Lu
Ram I Mahato
University of Tennessee Health Science Center · US

Funding

Growth Factor and Antiapoptotic Gene Delivery to Human IsletsR01DK069968 · NIDDK · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI MAHATO, RAM I. · 2005 to 2012
$2.2M
NIDDK NIH HHS R01 DK069968NIDDK NIH HHS R01 DK69968
6 · The paper itself

Abstract

purposeTo evaluate the efficacy of human bone marrow-derived mesenchymal stem cells (hBMSCs) as gene delivery vehicles to simultaneously express human hepatocyte growth factor (HGF) and interleukin 1 receptor antagonist (IL-1Ra) to improve the outcome of islet transplantation.

methodsMorphology and islet-binding affinity of hBMSCs were checked by microscope. The expression of target genes and endogenous genes was determined by ELISA. Protection of islets by hBMSCs was evaluated in vitro by Calcein-AM/Propidium Iodide staining and in vivo by allogeneic islet transplantation study. Function and revascularization of islets was evaluated by immune fluorescence study.

resultsNon-donor-specific hBMSCs showed strong binding affinity to human islets and protected viability and function. Transduction of hBMSCs with adenovirus encoding human HGF and human IL-1Ra (Adv-hHGF-hIL-1Ra) prior to co-culturing with islets further protected from apoptotic cell death, helped maintain 3D structures and morphology, and enhanced insulin secretion. Transplantation of human islets reconstituted with Adv-hHGF-hIL-1Ra transduced hBMSCs under the kidney capsule of streptozotocin-induced diabetic non-obese diabetic/severe combined immunodeficient (NOD-SCID) mice reversed diabetes by reducing blood glucose levels to ≤ 200 mg/dL for up to 15 weeks and reduced the number of islets required to achieving normoglycemia. Blood glucose levels of mice transplanted with islets alone reversed to ≥ 500 mg/dL 4 weeks post-transplantation.

conclusionsResults indentified hBMSCs as effective gene delivery vehicles to improve the outcome of islet transplantation.

Indexed as

Gene Transfer TechniquesIslets of Langerhans TransplantationMesenchymal Stem CellsAdenoviridaeAnimalsBlood GlucoseDiabetes Mellitus, ExperimentalGenetic VectorsGlucose Tolerance TestGraft RejectionGraft SurvivalHepatocyte Growth FactorHumansInsulinInsulin SecretionInterleukin 1 Receptor Antagonist ProteinBlood GlucoseHepatocyte Growth FactorIL1RN protein, humanInsulinInterleukin 1 Receptor Antagonist Protein

Identifiers

PMID21499838
PMCPMC3152657
OpenAlexW2105599018

What OpenQuestion holds

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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.