Evidence map›Paper›PMID 26006248›Full record

ReviewInternational journal of molecular sciences2015

Biomedical application of low molecular weight heparin/protamine nano/micro particles as cell- and growth factor-carriers and coating matrix.

Masayuki Ishihara, Satoko Kishimoto, Makoto Takikawa, Hidemi Hattori, Shingo Nakamura, Masafumi Shimizu

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. [Research progress of growth factor sustained-release microspheres in fat transplantation].Zhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery · 2017
    Review
  12. 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

6 authors.

Masayuki IshiharaDivision of Biomedical Engineering Research Institute, National Defense Medical College, Saitama 359-8513, Japan. ishihara@ndmc.ac.jp.
Satoko KishimotoResearch Support Center, Dokkyo Medical University, Tochigi 321-0293, Japan. skishi@dokkyomed.ac.jp.
Makoto TakikawaDepartment of Medical Engineering, National Defense Medical College, Saitama 359-8513, Japan. drme003@ndmc.ac.jp.
Hidemi HattoriDivision of Biomedical Engineering Research Institute, National Defense Medical College, Saitama 359-8513, Japan. h2@ndmc.ac.jp.
Shingo NakamuraDivision of Biomedical Engineering Research Institute, National Defense Medical College, Saitama 359-8513, Japan. snaka@ndmc.ac.jp.
Masafumi ShimizuDepartment of Surgery, Tokorozawa Meisei Hospital, Saitama 359-1145, Japan. masafumi@tokorozawameisei.or.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Low molecular weight heparin (LMWH)/protamine (P) nano/micro particles (N/MPs) (LMWH/P N/MPs) were applied as carriers for heparin-binding growth factors (GFs) and for adhesive cells including adipose-derived stromal cells (ADSCs) and bone marrow-derived mesenchymal stem cells (BMSCs). A mixture of LMWH and P yields a dispersion of N/MPs (100 nm-3 μm in diameter). LMWH/P N/MPs can be immobilized onto cell surfaces or extracellular matrix, control the release, activate GFs and protect various GFs. Furthermore, LMWH/P N/MPs can also bind to adhesive cell surfaces, inducing cells and LMWH/P N/MPs-aggregate formation. Those aggregates substantially promoted cellular viability, and induced vascularization and fibrous tissue formation in vivo. The LMWH/P N/MPs, in combination with ADSCs or BMSCs, are effective cell-carriers and are potential promising novel therapeutic agents for inducing vascularization and fibrous tissue formation in ischemic disease by transplantation of the ADSCs and LMWH/P N/MPs-aggregates. LMWH/P N/MPs can also bind to tissue culture plates and adsorb exogenous GFs or GFs from those cells. The LMWH/P N/MPs-coated matrix in the presence of GFs may provide novel biomaterials that can control cellular activity such as growth and differentiation. Furthermore, three-dimensional (3D) cultures of cells including ADSCs and BMSCs using plasma-medium gel with LMWH/P N/MPs exhibited efficient cell proliferation. Thus, LMWH/P N/MPs are an adequate carrier both for GFs and for stromal cells such as ADSCs and BMSCs, and are a functional coating matrix for their cultures.

Indexed as

Adipose TissueAnimalsBiocompatible MaterialsBone Marrow CellsCell- and Tissue-Based TherapyCell Culture TechniquesCell ProliferationCells, CulturedCell SurvivalDrug CarriersHeparin, Low-Molecular-WeightHumansIntercellular Signaling Peptides and ProteinsMesenchymal Stem CellsPlatelet-Rich PlasmaProtaminesBiocompatible MaterialsDrug CarriersHeparin, Low-Molecular-WeightIntercellular Signaling Peptides and ProteinsProtaminesadipose-derived stromal cellsbone marrow-derived mesenchymal stem cellscell delivery systemscoating matrixnano/micro particles

Identifiers

PMID26006248
PMCPMC4463730

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.