Evidence map›Paper›PMID 30573681›Full record

ArticleThe Journal of biological chemistry2019

Interleukin 34 (IL-34) cell-surface localization regulated by the molecular chaperone 78-kDa glucose-regulated protein facilitates the differentiation of monocytic cells.

Sayaka Ogawa, Yukiko Matsuoka, Miho Takada, Kazue Matsui, Fumihiro Yamane, Eri Kubota, Shiori Yasuhara, Kentaro Hieda, Naoki Kanayama, Naoya Hatano and 2 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 36% 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

6 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. The M-CSF receptor in osteoclasts and beyond.Experimental & molecular medicine · 2020
    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

12 authors at 3 institutions in 5 countries.

Sayaka OgawaFrom the Division of Medical Bioengineering, Graduate School of Natural Science and Technology.
Yukiko MatsuokaFrom the Division of Medical Bioengineering, Graduate School of Natural Science and Technology.
Miho TakadaFrom the Division of Medical Bioengineering, Graduate School of Natural Science and Technology.
Kazue MatsuiFrom the Division of Medical Bioengineering, Graduate School of Natural Science and Technology.
Fumihiro YamaneFrom the Division of Medical Bioengineering, Graduate School of Natural Science and Technology.
Eri Kubotathe Department of Applied Chemistry and Biotechnology, Faculty of Engineering, and.
Shiori YasuharaFrom the Division of Medical Bioengineering, Graduate School of Natural Science and Technology.
Kentaro HiedaFrom the Division of Medical Bioengineering, Graduate School of Natural Science and Technology.
Naoki KanayamaFrom the Division of Medical Bioengineering, Graduate School of Natural Science and Technology.
Naoya Hatanothe Laboratory of Applied Cell Biology, Graduate School of Interdisciplinary Science and Engineering in Health Systems, Okayama University, Tsushima-Naka 3-1-1, Kita-ku, Okayama 700-8530, Japan.
Hiroshi TokumitsuFrom the Division of Medical Bioengineering, Graduate School of Natural Science and Technology.ORCID 0000-0002-2193-6794
Masaki MagariFrom the Division of Medical Bioengineering, Graduate School of Natural Science and Technology, magari@cc.okayama-u.ac.jp.
Bioengineering Center · RUOkayama University · JPDepartment of Biotechnology · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interleukin 34 (IL-34) constitutes a cytokine that shares a common receptor, colony-stimulating factor-1 receptor (CSF-1R), with CSF-1. We recently identified a novel type of monocytic cell termed follicular dendritic cell-induced monocytic cells (FDMCs), whose differentiation depended on CSF-1R signaling through the IL-34 produced from a follicular dendritic cell line, FL-Y. Here, we report the functional mechanisms of the IL-34-mediated CSF-1R signaling underlying FDMC differentiation. CRIPSR/Cas9-mediated knockout of the

Indexed as

AnimalsCell DifferentiationCell LineCell MembraneDendritic Cells, FollicularEndoplasmic Reticulum Chaperone BiPGene Expression RegulationHeat-Shock ProteinsInterleukinsMaleMiceMice, Inbred BALB CMonocytesEndoplasmic Reticulum Chaperone BiPHeat-Shock ProteinsHspa5 protein, mouseinterleukin-34, mouseInterleukinscell differentiationcell surface proteinchaperonecolony-stimulating factor-1 receptorCRISPR/Cascytokinefollicular dendritic cellGRP78interleukininterleukin 34monocyteplasma membraneWestern blot

Identifiers

PMID30573681
PMCPMC6378969
OpenAlexW2905716194

What OpenQuestion holds

Textmetadata
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.