Evidence map›Paper›PMID 35406658›Full record

ArticleCells2022

Development of a Chemical Cocktail That Rescues Mouse Brain Demyelination in a Cuprizone-Induced Model.

Pei-Lun Lai, Chi-Hou Ng, Chia-Hsin Wu, Chien-Ying Lai, Scott C Schuyler, Vicki Wang, Hsuan Lin, Yueh-Chang Lee, Ming-Hsi Chuang, Chang-Huan Yang and 3 more

Abstract read
In one paragraph

Article in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

13 authors.

Pei-Lun LaiGenomics Research Center, Academia Sinica, Taipei 11529, Taiwan.
Chi-Hou NgGenomics Research Center, Academia Sinica, Taipei 11529, Taiwan.ORCID 0000-0002-2176-8655
Chia-Hsin WuGenomics Research Center, Academia Sinica, Taipei 11529, Taiwan.ORCID 0000-0002-8389-6599
Chien-Ying LaiGenomics Research Center, Academia Sinica, Taipei 11529, Taiwan.
Scott C SchuylerDepartment of Biomedical Sciences, College of Medicine, Chang Gung University, Taoyuan 33302, Taiwan.
Vicki WangTranslational Medicine, National Defense Medical Center, Academia Sinica, Taipei 11490, Taiwan.
Hsuan LinTaiwan International Graduate Program in Molecular Medicine, National Yang Ming Chiao Tung University, Academia Sinica, Taipei 11221, Taiwan.ORCID 0000-0002-7069-8040
Yueh-Chang LeeGenomics Research Center, Academia Sinica, Taipei 11529, Taiwan.
Ming-Hsi ChuangCollege of Management, Chung Hua University, Hsinchu 30012, Taiwan.
Chang-Huan YangGwo Xi Stem Cell Applied Technology Co., Ltd., Hsinchu 30261, Taiwan.
Wei-Ju ChenGenomics Research Center, Academia Sinica, Taipei 11529, Taiwan.
Hsiao-Chun HuangGenome and Systems Biology Degree Program, College of Life Science, National Taiwan University, Taipei 10617, Taiwan.ORCID 0000-0002-6556-3440
Jean LuGenomics Research Center, Academia Sinica, Taipei 11529, Taiwan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oligodendrocytes are glial cells located in the central nervous system (CNS) that play essential roles in the transmission of nerve signals and in the neuroprotection of myelinated neurons. The dysfunction or loss of oligodendrocytes leads to demyelinating diseases such as multiple sclerosis (MS). To treat demyelinating diseases, the development of a therapy that promotes remyelination is required. In the present study, we established an in vitro method to convert human fibroblasts into induced oligodendrocyte-like cells (iOLCs) in 3 days. The induced cells displayed morphologies and molecular signatures similar to oligodendrocytes after treatment with valproic acid and exposure to the small molecules Y27632, SU9516, and forskolin (FSK). To pursue the development of a cell-free remyelination therapy in vivo, we used a cuprizone-induced demyelinated mouse model. The small molecules (Y27632, SU9516, and FSK) were directly injected into the demyelinated corpus callosum of the mouse brain. This combination of small molecules rescued the demyelination phenotype within two weeks as observed by light and electron microscopy. These results provide a foundation for exploring the development of a treatment for demyelinating diseases via regenerative medicine.

Indexed as

CuprizoneDemyelinating DiseasesAnimalsCorpus CallosumMiceMice, Inbred C57BLOligodendrogliaCuprizonecuprizone-induced modeldemyelinationinduced oligodendrocyte-like cells (iOLCs)multiple sclerosis (MS)oligodendrocyte progenitor cells (OPCs)oligodendrocytesremyelination

Identifiers

PMID35406658
PMCPMC8997971

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.