Evidence map›Paper›PMID 11257120›Full record

ArticleThe Journal of cell biology2001

The high mobility group (HMG) boxes of the nuclear protein HMG1 induce chemotaxis and cytoskeleton reorganization in rat smooth muscle cells.

B Degryse, T Bonaldi, P Scaffidi, S Müller, M Resnati, F Sanvito, G Arrigoni, M E Bianchi

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 180 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
180citing papers in PubMed, 1 pooled it
18.6field-weighted citation impact, top 1% 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

180 citing papers in PubMed, 1 synthesis or guideline pooled it, 449 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. HMGB1 as a danger signal in vascular remodeling.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2026
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  6. HMGB1 Mediates Macrophage Recruitment and Regional Intervertebral Disc Properties Following Injury.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
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  19. Targeting HMGB1: An available Therapeutic Strategy for Breast Cancer Therapy.International journal of biological sciences · 2022
    Review
  20. Review

120 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

8 authors at 2 institutions in 1 country.

B DegryseDepartment of Genetics and Microbiology, University of Milan, 20133 Milan, Italy. degryse@scripps.edu
T Bonaldi
P Scaffidi
S Müller
M Resnati
F Sanvito
G Arrigoni
M E Bianchi
San Raffaele University of Rome · ITUniversity of Milan · IT

Funding

Telethon A.094
6 · The paper itself

Abstract

HMG1 (high mobility group 1) is a ubiquitous and abundant chromatin component. However, HMG1 can be secreted by activated macrophages and monocytes, and can act as a mediator of inflammation and endotoxic lethality. Here we document a role of extracellular HMG1 in cell migration. HMG1 (and its individual DNA-binding domains) stimulated migration of rat smooth muscle cells in chemotaxis, chemokinesis, and wound healing assays. HMG1 induced rapid and transient changes of cell shape, and actin cytoskeleton reorganization leading to an elongated polarized morphology typical of motile cells. These effects were inhibited by antibodies directed against the receptor of advanced glycation endproducts, indicating that the receptor of advanced glycation endproducts is the receptor mediating the HMG1-dependent migratory responses. Pertussis toxin and the mitogen-activated protein kinase kinase inhibitor PD98059 also blocked HMG1-induced rat smooth muscle cell migration, suggesting that a G(i/o) protein and mitogen-activated protein kinases are required for the HMG1 signaling pathway. We also show that HMG1 can be released by damage or necrosis of a variety of cell types, including endothelial cells. Thus, HMG1 has all the hallmarks of a molecule that can promote atherosclerosis and restenosis after vascular damage.

Indexed as

AnimalsCells, CulturedCell SizeChemotactic FactorsChemotaxisCulture Media, Serum-FreeCytoskeletonEndothelium, VascularEnzyme InhibitorsFlavonoidsGlycation End Products, AdvancedHigh Mobility Group ProteinsHumansMicroscopy, FluorescenceMitogen-Activated Protein Kinase KinasesMuscle, Smooth, Vascular2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-oneChemotactic FactorsCulture Media, Serum-FreeEnzyme InhibitorsFlavonoidsGlycation End Products, AdvancedHigh Mobility Group ProteinsMitogen-Activated Protein Kinase KinasesNuclear ProteinsPertussis ToxinReceptor for Advanced Glycation End ProductsReceptors, ImmunologicRecombinant ProteinsVirulence Factors, Bordetella

Identifiers

PMID11257120
PMCPMC2199202
OpenAlexW2128426645

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.