Evidence map›Paper›PMID 34602056›Full record

ArticleMolecular medicine (Cambridge, Mass.)2021

The collagen structure of C1q induces wound healing by engaging discoidin domain receptor 2.

Ria Aryani Hayuningtyas, Myeonggil Han, Seoyeon Choi, Man Sup Kwak, In Ho Park, Ji-Hyun Lee, Ji Eun Choi, Dae Ki Kim, Myoungsun Son, Jeon-Soo Shin

Open access · goldAbstract read
In one paragraph

Article in Molecular medicine (Cambridge, Mass.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

16 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
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  13. C1q and central nervous system disorders.Frontiers in immunology · 2023
    Review
  14. Article
  15. Macrophage-Specific,International journal of molecular sciences · 2022
    Article
  16. 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

10 authors at 4 institutions in 2 countries.

Ria Aryani Hayuningtyas *Department of Microbiology, Yonsei University College of Medicine, 50-1 Yonsei-ro Seodaemun-gu, Seoul, 03722, Republic of Korea.
Myeonggil Han *Department of Microbiology, Yonsei University College of Medicine, 50-1 Yonsei-ro Seodaemun-gu, Seoul, 03722, Republic of Korea.
Seoyeon ChoiDepartment of Microbiology, Yonsei University College of Medicine, 50-1 Yonsei-ro Seodaemun-gu, Seoul, 03722, Republic of Korea.
Man Sup KwakDepartment of Microbiology, Yonsei University College of Medicine, 50-1 Yonsei-ro Seodaemun-gu, Seoul, 03722, Republic of Korea.
In Ho ParkSeverance Biomedical Science Institute and Institute for Immunology and Immunological Diseases, Yonsei University College of Medicine, Seoul, 03722, Republic of Korea.
Ji-Hyun LeeDepartment of Immunology and Institute for Medical Sciences, Jeonbuk National University, Medical School, Jeonju, Jeollabuk-do, 54907, Republic of Korea.
Ji Eun ChoiDepartment of Pediatrics, Seoul National University Boramae Hospital, Seoul National University College of Medicine, Seoul, 07061, Republic of Korea.
Dae Ki KimDepartment of Immunology and Institute for Medical Sciences, Jeonbuk National University, Medical School, Jeonju, Jeollabuk-do, 54907, Republic of Korea.
Myoungsun SonInstitute of Molecular Medicine, The Feinstein Institutes for Medical Research, 350 Community Drive, Manhasset, NY, 11030, USA. mson@northwell.edu.ORCID 0000-0002-0655-3859
Jeon-Soo ShinDepartment of Microbiology, Yonsei University College of Medicine, 50-1 Yonsei-ro Seodaemun-gu, Seoul, 03722, Republic of Korea. jsshin6203@yuhs.ac.
Yonsei University · KRJeonbuk National University · KRFeinstein Institute for Medical Research · USSeoul National University · KR

Funding

Mechanisms of polarization of monocytes by DAMPs/PAMPs and C1qR01AI135063 · NIAID · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI SON, MYOUNGSUN · 2018 to 2022
$2.1M
NIAID NIH HHS R01 AI135063
6 · The paper itself

Abstract

backgroundC1q has been reported to reveal complement-independent roles in immune and non-immune cells. C1q binds to its specific receptors to regulate distinct functions that rely on the environment and cell types. Discoidin domain receptor 2 (DDR2) is activated by collagen and functions in wound healing by controlling matrix metalloproteinase (MMP) expression. Since C1q exhibits a collagen-like structure, we hypothesized that C1q might engage DDR2 to regulate wound healing and extracellular matrix (ECM) remodeling.

methodsCell-based assay, proximity ligation assay, ELISA, and surface plasmon analysis were utilized to investigate DDR2 and C1q binding. We also investigate the C1q-mediated in vitro wound healing ability using the human fibrosarcoma cell line, HT1080.

resultsC1q induced the phosphorylation of DDR2, p38 kinase, and ERK1/2. C1q and DDR2 binding improved cell migration and induced MMP2 and MMP9 expression. DDR2-specific shRNA reduced C1q-mediated cell migration for wound healing.

conclusionsC1q is a new DDR2 ligand that promotes wound healing. These findings have therapeutic implications in wound healing-related diseases.

Indexed as

Amino Acid SequenceCell Line, TumorCell MovementCollagenComplement C1qDiscoidin Domain Receptor 1Discoidin Domain Receptor 2HumansMatrix Metalloproteinase 2Matrix Metalloproteinase 9Microscopy, ConfocalPeptidesPhosphorylationProtein BindingSignal TransductionWound HealingC1QA protein, humanCollagenComplement C1qDiscoidin Domain Receptor 1Discoidin Domain Receptor 2Matrix Metalloproteinase 2Matrix Metalloproteinase 9MMP2 protein, humanMMP9 protein, humanPeptidesC1qCollagenDDR2Wound healing

Identifiers

PMID34602056
PMCPMC8489103
OpenAlexW3204032060

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.