Evidence map›Paper›PMID 35742968›Full record

ArticleInternational journal of molecular sciences2022

Characterization of the Secretome of a Specific Cell Expressing Mutant Methionyl-tRNA Synthetase in Co-Culture Using Click Chemistry.

Sungho Shin, Seonjeong Lee, Sunyoung Choi, Narae Park, Yumi Kwon, Jaehoon Jeong, Shinyeong Ju, Yunsil Chang, Kangsik Park, Chulwon Ha and 1 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
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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

11 authors.

Sungho ShinChemical & Biological Integrative Research Center, Korea Institute of Science and Technology, Seoul 02792, Korea.ORCID 0000-0002-4206-1229
Seonjeong LeeChemical & Biological Integrative Research Center, Korea Institute of Science and Technology, Seoul 02792, Korea.
Sunyoung ChoiDepartment of Orthopedic Surgery, Samsung Medical Center, School of Medicine, Sungkyunkwan University, Seoul 06351, Korea.
Narae ParkChemical & Biological Integrative Research Center, Korea Institute of Science and Technology, Seoul 02792, Korea.
Yumi KwonChemical & Biological Integrative Research Center, Korea Institute of Science and Technology, Seoul 02792, Korea.
Jaehoon JeongDivision of Radiation Biomedical Research, Korea Institute of Radiological and Medical Sciences, Seoul 01812, Korea.
Shinyeong JuChemical & Biological Integrative Research Center, Korea Institute of Science and Technology, Seoul 02792, Korea.
Yunsil ChangCell and Gene Therapy Institute, Samsung Medical Center, Seoul 06351, Korea.
Kangsik ParkKHU-KIST Department of Converging Science and Technology, Graduate School, Kyung Hee University, Seoul 02447, Korea.
Chulwon HaDepartment of Orthopedic Surgery, Samsung Medical Center, School of Medicine, Sungkyunkwan University, Seoul 06351, Korea.ORCID 0000-0001-5123-6513
Cheolju LeeChemical & Biological Integrative Research Center, Korea Institute of Science and Technology, Seoul 02792, Korea.ORCID 0000-0001-8482-4696

Funding

Korea Health Industry Development Institute HI14C3484Korea Institute of Science and Technology intramural programNational Research Foundation of Korea 2017M3A9F9030559National Research Foundation of Korea 2017M3C9A5031595
6 · The paper itself

Abstract

Co-culture system, in which two or more distinct cell types are cultured together, is advantageous in that it can mimic the environment of the in vivo niche of the cells. In this study, we presented a strategy to analyze the secretome of a specific cell type under the co-culture condition in serum-supplemented media. For the cell-specific secretome analysis, we expressed the mouse mutant methionyl-tRNA synthetase for the incorporation of the non-canonical amino acid, azidonorleucine into the newly synthesized proteins in cells of which the secretome is targeted. The azidonorleucine-tagged secretome could be enriched, based on click chemistry, and distinguished from any other contaminating proteins, either from the cell culture media or the other cells co-cultured with the cells of interest. In order to have more reliable true-positive identifications of cell-specific secretory bodies, we established criteria to exclude any identified human peptide matched to bovine proteins. As a result, we identified a maximum of 719 secreted proteins in the secretome analysis under this co-culture condition. Last, we applied this platform to profile the secretome of mesenchymal stem cells and predicted its therapeutic potential on osteoarthritis based on secretome analysis.

Indexed as

Methionine-tRNA LigaseAnimalsCattleClick ChemistryCoculture TechniquesMiceProteinsSecretomeMethionine-tRNA LigaseProteinsazidonorleucineBONCATclick chemistryco-culturemesenchymal stromal cellssecretome

Identifiers

PMID35742968
PMCPMC9223471

What OpenQuestion holds

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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.