Evidence map›Paper›PMID 31235582›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

Tracking the evolution of CNS remyelinating lesion in mice with neutral red dye.

Maryna Baydyuk, David S Cha, Jingwen Hu, Reiji Yamazaki, Evan M Miller, Victoria N Smith, Katherine A Kelly, Jeffrey K Huang

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

25 citing papers in PubMed, 47 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

8 authors at 1 institution in 1 country.

Maryna BaydyukDepartment of Biology, Georgetown University, Washington, DC 20057.
David S ChaDepartment of Biology, Georgetown University, Washington, DC 20057.
Jingwen HuDepartment of Biology, Georgetown University, Washington, DC 20057.
Reiji YamazakiDepartment of Biology, Georgetown University, Washington, DC 20057.
Evan M MillerDepartment of Biology, Georgetown University, Washington, DC 20057.
Victoria N SmithDepartment of Biology, Georgetown University, Washington, DC 20057.
Katherine A KellyDepartment of Biology, Georgetown University, Washington, DC 20057.
Jeffrey K HuangDepartment of Biology, Georgetown University, Washington, DC 20057; jh1659@georgetown.edu.ORCID 0000-0003-0996-9451
Georgetown University · US

Funding

Training in Neural Injury &PlasticityT32NS041218 · NINDS · GEORGETOWN UNIVERSITY · PI MARK P BURNS, Kathleen Anne Maguire-Zeiss · 2001 to 2026
$3.5M
Immunoregulation in CNS remyelinationR01NS107523 · NINDS · GEORGETOWN UNIVERSITY · PI HUANG, JEFFREY K · 2018 to 2022
$1.7M
Anti-inflammatory (M2) macrophage signaling in CNS remyelinationR21NS091890 · NINDS · GEORGETOWN UNIVERSITY · PI HUANG, JEFFREY K · 2015 to 2016
$428k
NINDS NIH HHS R01 NS107523NINDS NIH HHS R21 NS091890NINDS NIH HHS T32 NS041218
6 · The paper itself

Abstract

Animal models of central nervous system (CNS) demyelination, including toxin-induced focal demyelination and immune-mediated demyelination through experimental autoimmune encephalomyelitis (EAE), have provided valuable insights into the mechanisms of neuroinflammation and CNS remyelination. However, the ability to track changes in transcripts, proteins, and metabolites, as well as cellular populations during the evolution of a focal lesion, has remained challenging. Here, we developed a method to label CNS demyelinating lesions by the intraperitoneal injection of a vital dye, neutral red (NR), into mice before killing. We demonstrate that NR-labeled lesions can be easily identified on the intact spinal cord in both lysolecithin- and EAE-mediated demyelination models. Using fluorescence microscopy, we detected NR in activated macrophages/microglia and astrocytes, but not in oligodendrocytes present in lesions. Importantly, we successfully performed RT-qPCR, Western blot, flow cytometry, and mass spectrometry analysis of precisely dissected NR-labeled lesions at 5, 10, and 20 d postlesion (dpl) and found differential changes in transcripts, proteins, cell populations, and metabolites in lesions over the course of remyelination. Therefore, NR administration is a simple and powerful method to track and analyze the detailed molecular, cellular, and metabolic changes that occur within the lesion microenvironment over time following CNS injury. Furthermore, this method can be used to identify molecular and metabolic pathways that regulate neuroinflammation and remyelination and facilitate the development of therapies to promote repair in demyelinating disorders such as multiple sclerosis.

Indexed as

AnimalsAstrocytesCellular MicroenvironmentCentral Nervous SystemDemyelinating DiseasesDisease Models, AnimalFlow CytometryHumansLysophosphatidylcholinesMiceMicrogliaMultiple SclerosisMyelin SheathNerve RegenerationNervous System DiseasesNeutral RedLysophosphatidylcholinesNeutral Redanimal modelsdemyelinationinflammationremyelinationvital dye

Identifiers

PMID31235582
PMCPMC6628798
OpenAlexW2954515590

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.