Evidence map›Paper›PMID 31666601›Full record

ArticleScientific reports2019

Roles of monocarboxylate transporter subtypes in promotion and suppression of osteoclast differentiation and survival on bone.

Hiroko Imai, Kentaro Yoshimura, Yoichi Miyamoto, Kiyohito Sasa, Marika Sugano, Masahiro Chatani, Masamichi Takami, Matsuo Yamamoto, Ryutaro Kamijo

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

13 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Metabolite transporters as regulators of macrophage polarization.Naunyn-Schmiedeberg's archives of pharmacology · 2022
    Review
  12. Review
  13. Role of Altered Metabolic Microenvironment in Osteolytic Metastasis.Frontiers in cell and developmental biology · 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

9 authors at 1 institution in 1 country.

Hiroko ImaiDepartment of Biochemistry, Showa University School of Dentistry, Tokyo, Japan.
Kentaro YoshimuraDepartment of Biochemistry, Showa University School of Dentistry, Tokyo, Japan. kyoshimura@dent.showa-u.ac.jp.
Yoichi MiyamotoDepartment of Biochemistry, Showa University School of Dentistry, Tokyo, Japan.
Kiyohito SasaDepartment of Biochemistry, Showa University School of Dentistry, Tokyo, Japan.
Marika SuganoDepartment of Periodontology, Showa University School of Dentistry, Tokyo, Japan.
Masahiro ChataniDepartment of Pharmacology, Showa University School of Dentistry, Tokyo, Japan.
Masamichi TakamiDepartment of Pharmacology, Showa University School of Dentistry, Tokyo, Japan.ORCID http://orcid.org/0000-0002-4506-3975
Matsuo YamamotoDepartment of Periodontology, Showa University School of Dentistry, Tokyo, Japan.
Ryutaro KamijoDepartment of Biochemistry, Showa University School of Dentistry, Tokyo, Japan.
Showa University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Monocarboxylate transporters (MCTs) provide transmembrane transport of monocarboxylates such as lactate and pyruvate. The present results showed that α-cyano-4-hydroxycinnamic acid (CHC), an inhibitor of MCTs, promoted osteoclast differentiation from macrophages at lower concentrations (0.1-0.3 mM) and suppressed that at a higher concentration (1.0 mM). On the other hand, CHC reduced the number of mature osteoclasts on the surface of dentin in a concentration-dependent manner. Additionally, macrophages and osteoclasts were found to express the Mct1, Mct2, and Mct4 genes, with Mct1 and Mct4 expression higher in macrophages, and that of Mct2 higher in osteoclasts. Although Mct1 gene knockdown in macrophages enhanced osteoclast formation induced by RANKL, Mct2 gene knockdown suppressed that. Finally, Mct2 gene silencing in mature osteoclasts decreased their number and, thereby, bone resorption. These results suggest that MCT1 is a negative regulator and MCT2 a positive regulator of osteoclast differentiation, while MCT2 is required for bone resorption by osteoclasts.

Indexed as

Cell DifferentiationAnimalsBone and BonesBone Marrow CellsCell CountCell LineCell SurvivalCoumaric AcidsGene Expression RegulationGene SilencingHumansMacrophagesMaleMiceMonocarboxylic Acid TransportersOsteoclastsalpha-cyano-4-hydroxycinnamateCoumaric AcidsMonocarboxylic Acid TransportersRNA, Small Interfering

Identifiers

PMID31666601
PMCPMC6821745
OpenAlexW2982408039

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.