Evidence map›Paper›PMID 27183911›Full record

ArticleOncotarget2016

Nuclear delivery of recombinant OCT4 by chitosan nanoparticles for transgene-free generation of protein-induced pluripotent stem cells.

Salma Tammam, Peter Malak, Daphne Correa, Oliver Rothfuss, Hassan M E Azzazy, Alf Lamprecht, Klaus Schulze-Osthoff

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

8 citing papers in PubMed, 23 citations in OpenAlex.

  1. Repurpose but also (nano)-reformulate! The potential role of nanomedicine in the battle against SARS-CoV2.Journal of controlled release : official journal of the Controlled Release Society · 2021
    Review
  2. Cell-PermeableInternational journal of molecular sciences · 2021
    Article
  3. Article
  4. Article
  5. Application of iPSC to Modelling of Respiratory Diseases.Advances in experimental medicine and biology · 2020
    Review
  6. Review
  7. Article
  8. 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

7 authors at 4 institutions in 3 countries.

Salma TammamLaboratory of Pharmaceutical Technology and Biopharmaceutics, University of Bonn, 53121 Bonn, Germany.
Peter MalakInterfaculty Institute for Biochemistry, University of Tuebingen, 72076 Tuebingen, Germany.
Daphne CorreaInterfaculty Institute for Biochemistry, University of Tuebingen, 72076 Tuebingen, Germany.
Oliver RothfussInterfaculty Institute for Biochemistry, University of Tuebingen, 72076 Tuebingen, Germany.
Hassan M E AzzazyDepartment of Chemistry, The American University in Cairo, 11835 Cairo, Egypt.
Alf LamprechtLaboratory of Pharmaceutical Technology and Biopharmaceutics, University of Bonn, 53121 Bonn, Germany.
Klaus Schulze-OsthoffInterfaculty Institute for Biochemistry, University of Tuebingen, 72076 Tuebingen, Germany.
University of Tübingen · DEAmerican University in Cairo · EGUniversité de franche-comté · FRUniversity of Bonn · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Protein-based reprogramming of somatic cells is a non-genetic approach for the generation of induced pluripotent stem cells (iPSCs), whereby reprogramming factors, such as OCT4, SOX2, KLF4 and c-MYC, are delivered as functional proteins. The technique is considered safer than transgenic methods, but, unfortunately, most protein-based protocols provide very low reprogramming efficiencies. In this study, we developed exemplarily a nanoparticle (NP)-based delivery system for the reprogramming factor OCT4. To this end, we expressed human OCT4 in Sf9 insect cells using a baculoviral expression system. Recombinant OCT4 showed nuclear localization in Sf9 cells indicating proper protein folding. In comparison to soluble OCT4 protein, encapsulation of OCT4 in nuclear-targeted chitosan NPs strongly stabilized its DNA-binding activity even under cell culture conditions. OCT4-loaded NPs enabled cell treatment with high micromolar concentrations of OCT4 and successfully delivered active OCT4 into human fibroblasts. Chitosan NPs therefore provide a promising tool for the generation of transgene-free iPSCs.

Indexed as

Gene Transfer TechniquesActive Transport, Cell NucleusAnimalsBaculoviridaeCellular ReprogrammingChitosanFibroblastsHumansInduced Pluripotent Stem CellsInsectaKruppel-Like Factor 4NanoparticlesNuclear Localization SignalsOctamer Transcription Factor-3Protein BindingProtein FoldingChitosanKLF4 protein, humanKruppel-Like Factor 4Nuclear Localization SignalsOctamer Transcription Factor-3POU5F1 protein, humanchitosan nanoparticlesinduced pluripotent stem cellsOCT4reprogrammingtransgene-free stem cells

Identifiers

PMID27183911
PMCPMC5122344
OpenAlexW2399232819

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.