Evidence map›Paper›PMID 27473118›Full record

ArticleStem cell research & therapy2016

High-efficiency generation of induced pluripotent mesenchymal stem cells from human dermal fibroblasts using recombinant proteins.

Fanfan Chen, Guoqiang Zhang, Ling Yu, Yanye Feng, Xianghui Li, Zhijun Zhang, Yongting Wang, Dapeng Sun, Sriharsa Pradhan

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

18 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
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  7. Revisiting Epithelial Carcinogenesis.International journal of molecular sciences · 2022
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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

9 authors at 3 institutions in 2 countries.

Fanfan ChenShanghai R&D Center, New England Biolabs, Shanghai, 201203, China.
Guoqiang ZhangNew England Biolabs, Ipswich, MA, 01938, USA.
Ling YuShanghai R&D Center, New England Biolabs, Shanghai, 201203, China.
Yanye FengShanghai R&D Center, New England Biolabs, Shanghai, 201203, China.
Xianghui LiShanghai R&D Center, New England Biolabs, Shanghai, 201203, China.
Zhijun ZhangMed-X Research Institute of Shanghai Jiao Tong University, Shanghai, 200030, China.
Yongting WangMed-X Research Institute of Shanghai Jiao Tong University, Shanghai, 200030, China.
Dapeng SunShanghai R&D Center, New England Biolabs, Shanghai, 201203, China. dapeng_sun@163.com.
Sriharsa PradhanNew England Biolabs, Ipswich, MA, 01938, USA. pradhan@neb.com.
New England Biolabs (China) · CNNew England Biolabs (United States) · USShanghai Jiao Tong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInduced pluripotent mesenchymal stem cells (iPMSCs) are novel candidates for drug screening, regenerative medicine, and cell therapy. However, introduction of transcription factor encoding genes for induced pluripotent stem cell (iPSC) generation which could be used to generate mesenchymal stem cells is accompanied by the risk of insertional mutations in the target cell genome.

methodsWe demonstrate a novel method using an inactivated viral particle to package and deliver four purified recombinant Yamanaka transcription factors (Sox2, Oct4, Klf4, and c-Myc) resulting in reprogramming of human primary fibroblasts. Whole genome bisulfite sequencing was used to analyze genome-wide CpG methylation of human iPMSCs. Western blot, quantitative PCR, immunofluorescence, and in-vitro differentiation were used to assess the pluripotency of iPMSCs.

resultsThe resulting reprogrammed fibroblasts show high-level expression of stem cell markers. The human fibroblast-derived iPMSC genome showed gains in DNA methylation in low to medium methylated regions and concurrent loss of methylation in previously hypermethylated regions. Most of the differentially methylated regions are close to transcription start sites and many of these genes are pluripotent pathway associated. We found that DNA methylation of these genes is regulated by the four iPSC transcription factors, which functions as an epigenetic switch during somatic reprogramming as reported previously. These iPMSCs successfully differentiate into three embryonic germ layer cells, both in vitro and in vivo. Following multipotency induction in our study, the delivered transcription factors were degraded, leading to an improved efficiency of subsequent programmed differentiation.

conclusionRecombinant transcription factor based reprogramming and derivatization of iPMSC offers a novel high-efficiency approach for regenerative medicine from patient-derived cells.

Indexed as

Cellular ReprogrammingCell DifferentiationCpG IslandsDNA MethylationEpigenesis, GeneticFibroblastsGenetic VectorsGenome, HumanGerm LayersHumansInduced Pluripotent Stem CellsKruppel-Like Factor 4Kruppel-Like Transcription FactorsOctamer Transcription Factor-3Primary Cell CultureProto-Oncogene Proteins c-mycKLF4 protein, humanKruppel-Like Factor 4Kruppel-Like Transcription FactorsMYC protein, humanOctamer Transcription Factor-3POU5F1 protein, humanProto-Oncogene Proteins c-mycRecombinant ProteinsSOX2 protein, humanSOXB1 Transcription FactorsInactivated viral particleInduced pluripotent mesenchymal stem cellInduced pluripotent stem cellIn-vitro differentiationWhole genome bisulfite sequencing

Identifiers

PMID27473118
PMCPMC4967313
OpenAlexW2504492994

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.