Evidence map›Paper›PMID 28558818›Full record

ArticleJournal of neuroinflammation2017

MicroRNA-101a regulates microglial morphology and inflammation.

Reiko Saika, Hiroshi Sakuma, Daisuke Noto, Shuhei Yamaguchi, Takashi Yamamura, Sachiko Miyake

Open access · goldAbstract read
In one paragraph

Article in Journal of neuroinflammation, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
1.5field-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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 44 citations in OpenAlex.

  1. Pooled it
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  14. Transcriptomics in Alzheimer's Disease: Aspects and Challenges.International journal of molecular sciences · 2020
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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

6 authors at 3 institutions in 1 country.

Reiko SaikaDepartment of Immunology, National Institute of Neuroscience, National Center of Neurology and Psychiatry, 4-1-1, Ogawahigashi-cho, Kodaira, Tokyo, Japan.
Hiroshi SakumaDepartment of Immunology, National Institute of Neuroscience, National Center of Neurology and Psychiatry, 4-1-1, Ogawahigashi-cho, Kodaira, Tokyo, Japan.
Daisuke NotoDepartment of Immunology, National Institute of Neuroscience, National Center of Neurology and Psychiatry, 4-1-1, Ogawahigashi-cho, Kodaira, Tokyo, Japan.
Shuhei YamaguchiDepartment of Neurology, Shimane University Faculty of Medicine, 89-1 Enya-cho, Izumo, Shimane, Japan.
Takashi YamamuraDepartment of Immunology, National Institute of Neuroscience, National Center of Neurology and Psychiatry, 4-1-1, Ogawahigashi-cho, Kodaira, Tokyo, Japan.
Sachiko MiyakeDepartment of Immunology, National Institute of Neuroscience, National Center of Neurology and Psychiatry, 4-1-1, Ogawahigashi-cho, Kodaira, Tokyo, Japan. s-miyake@juntendo.ac.jp.
National Center of Neurology and Psychiatry · JPShimane University · JPTokyo Metropolitan Institute of Medical Science · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMicroglia, as well as other tissue-resident macrophages, arise from yolk sac progenitors. Thus, it is likely that the central nervous system environment is critical for the acquisition of a distinct microglial phenotype. Several microRNAs that are enriched in the brain play crucial roles in brain development and may also play a role in the differentiation of microglia.

methodsTo track the differentiation of hematopoietic cells into microglia, lineage-negative bone marrow cells were co-cultured with astrocytes in the absence or presence of microRNAs or their inhibitors. Microglia-like cells were identified as small, round cells that were immunopositive for CD11b, Iba1, CX3CR1, and triggering receptor expressed on myeloid cells (TREM)-2.

resultsFive microRNAs (miR-101a, miR-139-3p, miR-214

conclusionsmiR-101a, which is enriched in the brain, promotes the differentiation of bone marrow cells into microglia-like cells.

Indexed as

Analysis of VarianceAnimalsAnimals, NewbornCalcium-Binding ProteinsCell DifferentiationCell ProliferationCells, CulturedCoculture TechniquesDisease Models, AnimalFemaleGreen Fluorescent ProteinsInflammationMacrophagesMiceMice, Inbred C57BLMice, TransgenicAif1 protein, mouseCalcium-Binding ProteinsGreen Fluorescent ProteinsMicrofilament ProteinsMicroRNAsMIRN101 microRNA, mouseOligonucleotides, AntisenseReceptors, ImmunologicTREM-2a receptorCytokineDifferentiationHematopoietic cellMicrogliamicroRNA-101a

Identifiers

PMID28558818
PMCPMC5450088
OpenAlexW2619834615

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.