Evidence map›Paper›PMID 30644388›Full record

ArticleNature communications2019

Chi3l3 induces oligodendrogenesis in an experimental model of autoimmune neuroinflammation.

Sarah C Starossom, Juliana Campo Garcia, Tim Woelfle, Silvina Romero-Suarez, Marta Olah, Fumihiro Watanabe, Li Cao, Ada Yeste, John J Tukker, Francisco J Quintana and 7 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

52 citing papers in PubMed, 75 citations in OpenAlex.

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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

17 authors at 6 institutions in 3 countries.

Sarah C StarossomInstitute for Medical Immunology, Charité - Universitätsmedizin Berlin, 13353, Berlin, Germany. sarah-christin.starossom@charite.de.
Juliana Campo GarciaInstitute for Medical Immunology, Charité - Universitätsmedizin Berlin, 13353, Berlin, Germany.
Tim WoelfleInstitute for Medical Immunology, Charité - Universitätsmedizin Berlin, 13353, Berlin, Germany.
Silvina Romero-SuarezInstitute for Medical Immunology, Charité - Universitätsmedizin Berlin, 13353, Berlin, Germany.
Marta OlahCenter for Neurologic Diseases, Department of Neurology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 02115, USA.
Fumihiro WatanabeLaboratory of Neural Stem Cells and Functional Neurogenetics, Department of Neurology-The Ohio State University Wexner Medical Center, Columbus, OH, 43210, USA.
Li CaoCenter for Neurologic Diseases, Department of Neurology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 02115, USA.
Ada YesteCenter for Neurologic Diseases, Department of Neurology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 02115, USA.
John J TukkerNeuroscience Research Center (NWFZ), Charité - Universitätsmedizin Berlin, 10117, Berlin, Germany.ORCID http://orcid.org/0000-0002-4394-199X
Francisco J QuintanaCenter for Neurologic Diseases, Department of Neurology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 02115, USA.
Jaime ImitolaCenter for Neurologic Diseases, Department of Neurology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 02115, USA.ORCID http://orcid.org/0000-0003-2008-3133
Franziska WitzelIRI Life Sciences, Institute of Pathology, Computational Modeling in Medicine, Charité- Universitätsmedizin Berlin, 10117, Berlin, Germany.
Dietmar SchmitzNeuroCure Clinical Research Center, Charité - Universitätsmedizin Berlin, 10117, Berlin, Germany.
Markus MorkelInstitute of Pathology, Laboratory of Molecular Tumor Pathology and Systems Biology, Charité - Universitätsmedizin Berlin, 10117, Berlin, Germany.ORCID http://orcid.org/0000-0002-2553-9999
Friedemann PaulExperimental and Clinical Research Center, Max Delbrueck Center for Molecular Medicine and Charité - Universitätsmedizin Berlin, Berlin, Germany.
Carmen Infante-DuarteInstitute for Medical Immunology, Charité - Universitätsmedizin Berlin, 13353, Berlin, Germany.
Samia J KhouryCenter for Neurologic Diseases, Department of Neurology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 02115, USA.
Brigham and Women's Hospital · USCharité - Universitätsmedizin Berlin · DEBerlin Institute of Health at Charité - Universitätsmedizin Berlin · DEGerman Center for Neurodegenerative Diseases · DEMax Delbrück Center · DEThe Ohio State University Wexner Medical Center · US

Funding

Immune Regulation of Neural Stem Cell Program In EAER01AI043496 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI KHOURY, SAMIA J. · 1999 to 2015
$3.9M
NIAID NIH HHS R01 AI043496
6 · The paper itself

Abstract

In demyelinating diseases including multiple sclerosis (MS), neural stem cells (NSCs) can replace damaged oligodendrocytes if the local microenvironment supports the required differentiation process. Although chitinase-like proteins (CLPs) form part of this microenvironment, their function in this differentiation process is unknown. Here, we demonstrate that murine Chitinase 3-like-3 (Chi3l3/Ym1), human Chi3L1 and Chit1 induce oligodendrogenesis. In mice, Chi3l3 is highly expressed in the subventricular zone, a stem cell niche of the adult brain, and in inflammatory brain lesions during experimental autoimmune encephalomyelitis (EAE). We find that silencing Chi3l3 increases severity of EAE. We present evidence that in NSCs Chi3l3 activates the epidermal growth factor receptor (EGFR), thereby inducing Pyk2-and Erk1/2- dependent expression of a pro-oligodendrogenic transcription factor signature. Our results implicate CLP-EGFR-Pyk2-MEK-ERK as a key intrinsic pathway controlling oligodendrogenesis.

Indexed as

Animalsbeta-N-AcetylhexosaminidasesChitinase-3-Like Protein 1Encephalomyelitis, Autoimmune, ExperimentalErbB ReceptorsFemaleHEK293 CellsHexosaminidasesHumansLectinsMAP Kinase Signaling SystemMiceNeural Stem CellsOligodendrogliabeta-N-AcetylhexosaminidasesCHI3L1 protein, humanChil3 protein, mouseChitinase-3-Like Protein 1chitotriosidaseEGFR protein, mouseErbB ReceptorsHexosaminidasesLectins

Identifiers

PMID30644388
PMCPMC6333780
OpenAlexW2909801310

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.