Evidence map›Paper›PMID 25876057›Full record

ArticlePloS one2015

Melatonin inhibits embryonic salivary gland branching morphogenesis by regulating both epithelial cell adhesion and morphology.

Aya Obana-Koshino, Hitomi Ono, Jiro Miura, Manabu Sakai, Hitoshi Uchida, Wataru Nakamura, Kanji Nohara, Yusuke Maruyama, Atsuhiko Hattori, Takayoshi Sakai

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 34% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
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

10 authors at 3 institutions in 1 country.

Aya Obana-KoshinoDepartment of Oral-facial Disorders, Osaka University Graduate School of Dentistry, Suita, Osaka, Japan.
Hitomi OnoDepartment of Oral-facial Disorders, Osaka University Graduate School of Dentistry, Suita, Osaka, Japan.
Jiro MiuraDivision for Interdisciplinary Dentistry, Osaka University Graduate School of Dentistry, Suita, Osaka, Japan.
Manabu SakaiClinical Laboratory, Osaka University Dental Hospital, Suita, Osaka, Japan.
Hitoshi UchidaDepartment of Oral-facial Disorders, Osaka University Graduate School of Dentistry, Suita, Osaka, Japan; Laboratory of Oral Chronobiology, Osaka University Graduate School of Dentistry, Suita, Osaka, Japan.
Wataru NakamuraLaboratory of Oral Chronobiology, Osaka University Graduate School of Dentistry, Suita, Osaka, Japan.
Kanji NoharaDepartment of Oral-facial Disorders, Osaka University Graduate School of Dentistry, Suita, Osaka, Japan.
Yusuke MaruyamaDepartment of Biology, Tokyo Medical and Dental University, Ichikawa, Chiba, Japan.
Atsuhiko HattoriDepartment of Biology, Tokyo Medical and Dental University, Ichikawa, Chiba, Japan.
Takayoshi SakaiDepartment of Oral-facial Disorders, Osaka University Graduate School of Dentistry, Suita, Osaka, Japan.
Osaka University · JPTokyo Medical and Dental University · JPOsaka University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many organs, including salivary glands, lung, and kidney, are formed by epithelial branching during embryonic development. Branching morphogenesis occurs via either local outgrowths or the formation of clefts that subdivide epithelia into buds. This process is promoted by various factors, but the mechanism of branching morphogenesis is not fully understood. Here we have defined melatonin as a potential negative regulator or "brake" of branching morphogenesis, shown that the levels of it and its receptors decline when branching morphogenesis begins, and identified the process that it regulates. Melatonin has various physiological functions, including circadian rhythm regulation, free-radical scavenging, and gonadal development. Furthermore, melatonin is present in saliva and may have an important physiological role in the oral cavity. In this study, we found that the melatonin receptor is highly expressed on the acinar epithelium of the embryonic submandibular gland. We also found that exogenous melatonin reduces salivary gland size and inhibits branching morphogenesis. We suggest that this inhibition does not depend on changes in either proliferation or apoptosis, but rather relates to changes in epithelial cell adhesion and morphology. In summary, we have demonstrated a novel function of melatonin in organ formation during embryonic development.

Indexed as

MorphogenesisAnimalsApoptosisCell AdhesionCell ShapeEmbryonic DevelopmentEpithelial CellsFemaleGene Expression Regulation, DevelopmentalMelatoninMicePregnancyReceptor, Melatonin, MT1Receptor, Melatonin, MT2Salivary GlandsMelatoninReceptor, Melatonin, MT1Receptor, Melatonin, MT2

Identifiers

PMID25876057
PMCPMC4398443
OpenAlexW1969575165

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.