Evidence map›Paper›PMID 25170965›Full record

ArticlePloS one2014

Hyperosmotic stress reduces melanin production by altering melanosome formation.

Bum-Ho Bin, Jinhyuk Bhin, Seung Ha Yang, Dong-Hwa Choi, Kyuhee Park, Dong Wook Shin, Ai-Young Lee, Daehee Hwang, Eun-Gyung Cho, Tae Ryong Lee

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
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

14 citing papers in PubMed, 27 citations in OpenAlex.

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  11. The Development of Sugar-Based Anti-Melanogenic Agents.International journal of molecular sciences · 2016
    Review
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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

10 authors at 4 institutions in 1 country.

Bum-Ho BinBioscience Research Institute, Amorepacific Corporation R&D Center, Yongin, Republic of Korea.
Jinhyuk BhinDepartment of Chemical Engineering, POSTECH, Pohang, Republic of Korea.
Seung Ha YangBioscience Research Institute, Amorepacific Corporation R&D Center, Yongin, Republic of Korea.
Dong-Hwa ChoiGyeonggi Bio Center, Gyeonggi Institute of Science & Technology Promotion, Suwon, Republic of Korea.
Kyuhee ParkGyeonggi Bio Center, Gyeonggi Institute of Science & Technology Promotion, Suwon, Republic of Korea.
Dong Wook ShinBioscience Research Institute, Amorepacific Corporation R&D Center, Yongin, Republic of Korea.
Ai-Young LeeDepartment of Dermatology, Dongguk University Ilsan Hospital, Goyang, Republic of Korea.
Daehee HwangDepartment of Chemical Engineering, POSTECH, Pohang, Republic of Korea.
Eun-Gyung ChoBioscience Research Institute, Amorepacific Corporation R&D Center, Yongin, Republic of Korea.
Tae Ryong LeeBioscience Research Institute, Amorepacific Corporation R&D Center, Yongin, Republic of Korea.
Amorepacific (South Korea) · KRGyeonggi College of Science and Technology · KRPohang University of Science and Technology · KRDongguk University Ilsan Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many tissues of the human body encounter hyperosmotic stress. The effect of extracellular osmotic changes on melanin production has not yet been elucidated. In this study, we determined that hyperosmotic stress induced by organic osmolytes results in reduced melanin production in human melanoma MNT-1 cells. Under hyperosmotic stress, few pigmented mature melanosomes were detected, but there was an increase in swollen vacuoles. These vacuoles were stained with an anti-M6PR antibody that recognizes late endosomal components and with anti-TA99 and anti-HMB45 antibodies, implying that melanosome formation was affected by hyperosmotic stress. Electron microscopic analysis revealed that the M6PR-positive swollen vacuoles were multi-layered and contained melanized granules, and they produced melanin when L-DOPA was applied, indicating that these vacuoles were still capable of producing melanin, but the inner conditions were not compatible with melanin production. The vacuolation phenomenon induced by hyperosmotic conditions disappeared with treatment with the PI3K activator 740 Y-P, indicating that the PI3K pathway is affected by hyperosmotic conditions and is responsible for the proper formation and maturation of melanosomes. The microarray analysis showed alterations of the vesicle organization and transport under hyperosmotic stress. Our findings suggest that melanogenesis could be regulated by physiological conditions, such as osmotic pressure.

Indexed as

Antiparkinson AgentsBlotting, WesternCell Line, TumorCluster AnalysisGene Expression Profilinggp100 Melanoma AntigenHumansLevodopaMelaninsMelanocytesMelanomaMelanosomesMembrane GlycoproteinsMicroscopy, Electron, TransmissionMicroscopy, FluorescenceOligonucleotide Array Sequence AnalysisAntiparkinson Agentsgp100 Melanoma AntigenLevodopaMelaninsMembrane GlycoproteinsOxidoreductasesPhosphatidylinositol 3-KinasesPMEL protein, humanTYRP1 protein, human

Identifiers

PMID25170965
PMCPMC4149489
OpenAlexW1989374522

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.