Evidence map›Paper›PMID 26224135›Full record

ArticleScientific reports2015

Selective Generation of Dopaminergic Precursors from Mouse Fibroblasts by Direct Lineage Conversion.

Changhai Tian, Yuju Li, Yunlong Huang, Yongxiang Wang, Dapeng Chen, Jinxu Liu, Xiaobei Deng, Lijun Sun, Kristi Anderson, Xinrui Qi and 5 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

24 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
  2. Review
  3. Progress in direct reprogramming of dopaminergic cell replacement therapy.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2024
    Review
  4. Next-generation direct reprogramming.Frontiers in cell and developmental biology · 2024
    Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Direct cell-fate conversion of somatic cells: Toward regenerative medicine and industries.Proceedings of the Japan Academy. Series B, Physical and biological sciences · 2020
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. 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

15 authors at 5 institutions in 3 countries.

Changhai TianCenter for Translational Neurodegeneration and Regenerative Therapy, Shanghai Tenth People's Hospital affiliated to Tongji University School of Medicine, Shanghai 200072, China.
Yuju LiCenter for Translational Neurodegeneration and Regenerative Therapy, Shanghai Tenth People's Hospital affiliated to Tongji University School of Medicine, Shanghai 200072, China.
Yunlong HuangCenter for Translational Neurodegeneration and Regenerative Therapy, Shanghai Tenth People's Hospital affiliated to Tongji University School of Medicine, Shanghai 200072, China.
Yongxiang WangDepartment of Pharmacology and Experimental Neuroscience.
Dapeng ChenDepartment of Nephrology, Chinese PLA General Hospital, Beijing 100853, P. R. China.
Jinxu LiuDepartment of Emergency Medicine.
Xiaobei DengCenter for Translational Neurodegeneration and Regenerative Therapy, Shanghai Tenth People's Hospital affiliated to Tongji University School of Medicine, Shanghai 200072, China.
Lijun SunDepartment of Pathology and Microbiology.
Kristi AndersonDepartment of Pharmacology and Experimental Neuroscience.
Xinrui QiCenter for Translational Neurodegeneration and Regenerative Therapy, Shanghai Tenth People's Hospital affiliated to Tongji University School of Medicine, Shanghai 200072, China.
Yulong LiDepartment of Emergency Medicine.
R Lee MosleyDepartment of Pharmacology and Experimental Neuroscience.
Xiangmei ChenDepartment of Nephrology, Chinese PLA General Hospital, Beijing 100853, P. R. China.
Jian HuangChinese National Human Genome Center at Shanghai, Shanghai 201203, P.R. China.
Jialin C ZhengCenter for Translational Neurodegeneration and Regenerative Therapy, Shanghai Tenth People's Hospital affiliated to Tongji University School of Medicine, Shanghai 200072, China.
University of Nebraska Medical Center · USTongji University · CNChinese PLA General Hospital · CNChinese National Human Genome Center at Shanghai · CNShanghai Tenth People's Hospital · CN

Funding

VIRAL SHUTOFF OF HOST TRANSCRIPTION--PBCV-1 INFECTEDP20RR015635 · NCRR · UNIVERSITY OF NEBRASKA LINCOLN · PI WOOD, CHARLES · 2000 to 2009
$22.1M
TRAIL and glutaminase: neurotoxic link in HIV-1 DementiaR01NS041858 · NINDS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI ZHENG, JIALIN CHARLES · 2001 to 2014
$4.4M
SDF-1 and neurogenesis in HIV-1 associated dementiaR01NS061642 · NINDS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI ZHENG, JIALIN CHARLES · 2008 to 2012
$2.0M
T Cell-Mediated Neurodegeneration in Parkinson's DiseaseR01NS070190 · NINDS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI MOSLEY, R LEE · 2010 to 2014
$1.8M
NCRR NIH HHS P20 RR015635NCRR NIH HHS P20 RR15635-01NINDS NIH HHS R01 NS041858NINDS NIH HHS R01 NS061642NINDS NIH HHS R01 NS 061642-01NINDS NIH HHS R01 NS070190NINDS NIH HHS R01 NS 41858-01
6 · The paper itself

Abstract

Degeneration of midbrain dopaminergic (DA) neurons is a key pathological event of Parkinson's disease (PD). Limited adult dopaminergic neurogenesis has led to novel therapeutic strategies such as transplantation of dopaminergic precursors (DPs). However, this strategy is currently restrained by a lack of cell source, the tendency for the DPs to become a glial-restricted state, and the tumor formation after transplantation. Here, we demonstrate the direct conversion of mouse fibroblasts into induced DPs (iDPs) by ectopic expression of Brn2, Sox2 and Foxa2. Besides expression with neural progenitor markers and midbrain genes including Corin, Otx2 and Lmx1a, the iDPs were restricted to dopaminergic neuronal lineage upon differentiation. After transplantation into MPTP-lesioned mice, iDPs differentiated into DA neurons, functionally alleviated the motor deficits, and reduced the loss of striatal DA neuronal axonal termini. Importantly, no iDPs-derived astrocytes and neoplasia were detected in mouse brains after transplantation. We propose that the iDPs from direct reprogramming provides a safe and efficient cell source for PD treatment.

Indexed as

Action PotentialsAnimalsCell DifferentiationCell LineageCell ProliferationCells, CulturedDopaminergic NeuronsDoxorubicinFibroblastsHepatocyte Nuclear Factor 3-betaInduced Pluripotent Stem CellsLIM-Homeodomain ProteinsMaleMiceMice, Inbred C57BLMice, TransgenicCorin protein, mouseDoxorubicinFoxa2 protein, mouseHepatocyte Nuclear Factor 3-betaLIM-Homeodomain ProteinsLmx1a protein, mouseNerve Tissue ProteinsNes protein, mouseNestinOtx2 protein, mouseOtx Transcription FactorsPou3f2 protein, mousePOU Domain FactorsProto-Oncogene Proteins c-mycSerine EndopeptidasesSox2 protein, mouseSOXB1 Transcription FactorsTranscription Factors

Identifiers

PMID26224135
PMCPMC4519786
OpenAlexW2231325109

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.