Evidence map›Paper›PMID 33114438›Full record

ArticleNutrients2020

Cellular Function of Annexin A1 Protein Mimetic Peptide Ac2-26 in Human Skin Keratinocytes HaCaT and Fibroblast Detroit 551 Cells.

Seong Min Kim, Sang Eun Ha, Preethi Vetrivel, Hun Hwan Kim, Pritam Bhagwan Bhosale, Jung Eun Park, Jeong Doo Heo, Young Sil Kim, Gon Sup Kim

Open access · goldAbstract read
In one paragraph

Article in Nutrients, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 31% 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

3 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

9 authors at 2 institutions in 1 country.

Seong Min KimResearch Institute of Life Science and College of Veterinary Medicine, Gyeongsang National University, Jinju 52828, Korea.
Sang Eun HaResearch Institute of Life Science and College of Veterinary Medicine, Gyeongsang National University, Jinju 52828, Korea.
Preethi VetrivelResearch Institute of Life Science and College of Veterinary Medicine, Gyeongsang National University, Jinju 52828, Korea.
Hun Hwan KimResearch Institute of Life Science and College of Veterinary Medicine, Gyeongsang National University, Jinju 52828, Korea.
Pritam Bhagwan BhosaleResearch Institute of Life Science and College of Veterinary Medicine, Gyeongsang National University, Jinju 52828, Korea.ORCID 0000-0003-1691-7844
Jung Eun ParkT-Stem Co., Ltd., Gyeongsangnam-do, Changwon 51573, Korea.
Jeong Doo HeoBiological Resources Research Group, Bioenvironmental Science & Toxicology Division, Gyeongnam Branch Institute, Korea Institute of Toxicology (KIT), 17 Jeigok-gil, Jinju 52834, Korea.
Young Sil KimT-Stem Co., Ltd., Gyeongsangnam-do, Changwon 51573, Korea.
Gon Sup KimResearch Institute of Life Science and College of Veterinary Medicine, Gyeongsang National University, Jinju 52828, Korea.ORCID 0000-0002-0844-1009
Gyeongsang National University · KRKorea Institute of Toxicology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inflammation of the skin is the most common dermatological problem in human. The anti-inflammatory mediated responses of the skin cells provide a mechanism for combating these conditions. Annexin A1 (AnxA1) is one of the proteins that has been shown to have a potent anti-inflammatory effect. However, the effects and mechanisms of AnxA1 in skin keratinocyte and fibroblast have not been reported yet. In the current study, we hypothesized that Ac2-26, AnxA1 mimetic peptide, ameliorates inflammation and wrinkle formation in human skin cells. Therefore, we aimed to identify whether Ac2-26 has anti-inflammatory and anti-wrinkle effects in human keratinocyte (HaCaT) and fibroblast (Detroit 551) cells, respectively. Human HaCaT cells were stimulated by TNF-α/IFN-γ with or without Ac2-26, to identify the anti-inflammatory effect. Human Detroit 551 cells were treated with Ac2-26 to verify the anti-wrinkle effect. Initially, cell cytotoxicity was carried out in each cell line treated using Ac2-26 by MTT assay. Human MDA, IL-8, and procollagen secretion were detected by ELISA assay. The inflammatory chemokines were measured by qRT-PCR analysis. To demonstrate the mechanism, MAPK, NF-κB, JAK/STAT, and MMPs were analyzed by Western blotting. As a result, we identified that Ac2-26 significantly decreased the expression of TNF-α/IFN-γ-stimulated pro-inflammatory chemokines, including IL-1β, IL-6, IL-8, MDC, TARC, and TNF-α, by inhibiting the activation of MAPK, NF-κB, and JAK/STAT pathway in TNF-α/IFN-γ-stimulated HaCaT human keratinocytes. In addition, we also identified that Ac2-26 significantly induced collagen synthesis by generating pro-collagen, and suppressed collagen degradation by inhibiting the collagenase MMP-1 and MMP-8 expression. Collectively, these results suggest that Ac2-26 shows anti-inflammatory and anti-wrinkling effect. These effects may lead to the development of preventive and therapeutic application for inflammation-related skin disease and wrinkle formation.

Indexed as

Annexin A1Anti-Inflammatory AgentsBlotting, WesternCell LineChemokinesEnzyme-Linked Immunosorbent AssayFibroblastsHumansInterleukin-8KeratinocytesPeptidesProcollagenSignal TransductionSkin AgingAnnexin A1annexin A1 peptide (2-26)Anti-Inflammatory AgentsChemokinesInterleukin-8PeptidesProcollagenAc2-26annexin A1anti-inflammationanti-wrinkleskin disease

Identifiers

PMID33114438
PMCPMC7693871
OpenAlexW3094182188

What OpenQuestion holds

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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.