Evidence map›Paper›PMID 20952587›Full record

ArticleThe American journal of pathology2010

Angiopoietin-like 4 interacts with integrins beta1 and beta5 to modulate keratinocyte migration.

Yan Yih Goh, Mintu Pal, Han Chung Chong, Pengcheng Zhu, Ming Jie Tan, Lakshmi Punugu, Chee Ren Ivan Lam, Yin Hoe Yau, Chek Kun Tan, Royston-Luke Huang and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
6.5field-weighted citation impact, top 3% 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

66 citing papers in PubMed, 127 citations in OpenAlex.

  1. Article
  2. The PPARβ/Delta-Induced Mesenchymal Stromal Cell Secretome Has Cytoprotective Effects via ANGPTL4 in a Pre-Clinical Model of Acute Lung Inflammation.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  3. RelA Signaling inInternational journal of molecular sciences · 2026
    Article
  4. Article
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  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Dual role of ANGPTL4 in inflammation.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2023
    Review
  16. Primary tumor-derived systemic nANGPTL4 inhibits metastasis.The Journal of experimental medicine · 2023
    Article
  17. Article
  18. Article
  19. ANGPTL4 Regulates PsoriasisFrontiers in pharmacology · 2022
    Article
  20. The cellular and functional complexity of thermogenic fat.Nature reviews. Molecular cell biology · 2021
    Review

6 more citing papers are in PubMed but not listed here.

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

15 authors at 4 institutions in 2 countries.

Yan Yih GohSchool of Biological Sciences, Nanyang Technological University, Singapore 637551.
Mintu Pal
Han Chung Chong
Pengcheng Zhu
Ming Jie Tan
Lakshmi Punugu
Chee Ren Ivan Lam
Yin Hoe Yau
Chek Kun Tan
Royston-Luke Huang
Suet Mien Tan
Mark Boon Yang Tang
Jeak Ling Ding
Sander Kersten
Nguan Soon Tan
Nanyang Technological University · SGNational Skin Centre · SGNational University of Singapore · SGWageningen University & Research · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adipose tissue secretes adipocytokines for energy homeostasis, but recent evidence indicates that some adipocytokines also have a profound local impact on wound healing. Upon skin injury, keratinocytes use various signaling molecules to promote reepithelialization for efficient wound closure. In this study, we identify a novel function of adipocytokine angiopoietin-like 4 (ANGPTL4) in keratinocytes during wound healing through the control of both integrin-mediated signaling and internalization. Using two different in vivo models based on topical immuno-neutralization of ANGPTL4 as well as ablation of the ANGPTL4 gene, we show that ANGPTL4-deficient mice exhibit delayed wound reepithelialization with impaired keratinocyte migration. Human keratinocytes in which endogenous ANGPTL4 expression was suppressed by either siRNA or a neutralizing antibody show impaired migration associated with diminished integrin-mediated signaling. Importantly, we identify integrins β1 and β5, but not β3, as novel binding partners of ANGPTL4. ANGPTL4-bound integrin β1 activated the FAK-Src-PAK1 signaling pathway, which is important for cell migration. The findings presented herein reveal an unpredicted role of ANGPTL4 during wound healing and demonstrate how ANGPTL4 stimulates intracellular signaling mechanisms to coordinate cellular behavior. Our findings provide insight into a novel cell migration control mechanism and underscore the physiological importance of the modulation of integrin activity in cancer metastasis.

Indexed as

Cell MovementAngiopoietin-Like Protein 4AngiopoietinsAnimalsCell AdhesionIntegrin beta1Integrin beta ChainsKeratinocytesMiceMice, Inbred C57BLMice, KnockoutProtein BindingProtein TransportSignal TransductionSkinWound HealingAngiopoietin-Like Protein 4AngiopoietinsAngptl4 protein, mouseIntegrin beta1integrin beta5Integrin beta Chains

Identifiers

PMID20952587
PMCPMC2993291
OpenAlexW2110646133

What OpenQuestion holds

Textmetadata
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.