Evidence map›Paper›PMID 27100831›Full record

ArticlePloS one2016

High Mobility Group Box-1 Promotes Inflammation-Induced Lymphangiogenesis via Toll-Like Receptor 4-Dependent Signalling Pathway.

Longhui Han, Minglian Zhang, Mengmeng Wang, Jinchen Jia, Miying Zhao, Yiming Fan, Xiaorong Li

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

10 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. HMGB1 Antagonist, Box A, Reduces TLR4, RAGE, and Inflammatory Cytokines in the Cornea of P. aeruginosa-Infected Mice.Journal of ocular pharmacology and therapeutics : the official journal of the Association for Ocular Pharmacology and Therapeutics · 2018
    Article
  7. Article
  8. Article
  9. Review
  10. 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

7 authors at 3 institutions in 1 country.

Longhui HanTianjin Medical University Eye Hospital/Eye Institute, School of Optometry and Ophthalmology, Tianjin Medical University, Tianjin, China.
Minglian ZhangHebei Provincial Key Laboratory of Ophthalmology, Hebei Provincial Eye institute, Hebei Provincial Eye Hospital, Xingtai, Hebei, China.
Mengmeng WangHebei Provincial Key Laboratory of Ophthalmology, Hebei Provincial Eye institute, Hebei Provincial Eye Hospital, Xingtai, Hebei, China.
Jinchen JiaHebei Provincial Key Laboratory of Ophthalmology, Hebei Provincial Eye institute, Hebei Provincial Eye Hospital, Xingtai, Hebei, China.
Miying ZhaoHebei Provincial Key Laboratory of Ophthalmology, Hebei Provincial Eye institute, Hebei Provincial Eye Hospital, Xingtai, Hebei, China.
Yiming FanHebei Provincial Key Laboratory of Ophthalmology, Hebei Provincial Eye institute, Hebei Provincial Eye Hospital, Xingtai, Hebei, China.
Xiaorong LiTianjin Medical University Eye Hospital/Eye Institute, School of Optometry and Ophthalmology, Tianjin Medical University, Tianjin, China.
Hebei Eye Hospital · CNTianjin Medical University · CNTianjin Medical University Eye Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lymphangiogenesis in inflammation has received considerable attention in recent years. Administration of modulating lymphangiogenesis provides more possibilities of treating inflammation-associated diseases. However, the main mediators and factors governing inflammation-induced lymphangiogenesis (ILA) are yet to be defined. Here, we explored the role of HMGB1-TLR4 signalling pathway in modulating inflammation-induced lymphangiogenesis and its underlying mechanisms using an ILA mouse model and 2 cell lines. Our results show that HMGB1 promoted VEGF-C-induced HDLECs proliferation in a dose-dependent manner and TLR4 mediates HMGB1-induced LECs proliferation and tube formation in vitro. And in vivo, rHMGB1 treatment significantly promoted ILA, and the promoting effects was inhibited notably when HMGB1-TLR4 was blocked. HMGB1-associated ILA is primarily dependent on TLR4 but not on TLR2. In mechanisms, the recruitment and activation of CD11b+ cells are important cellular mechanisms in HMGB1-TLR4 associated ILA, and multiple key pro-lymphangiogenesis molecules mediates HMGB1-TLR4 associated ILA, including VEGF-C/VEGFR3, inflammatory factors IL-1β and TNF-α, MMP-2 and MMP-9 and NF-κB p65. In conclusion, HMGB1-associated ILA is primarily dependent on TLR4, and CD11b+ cells and multiple molecular mechanisms mediate HMGB1-TLR4 associated ILA. Furthermore, the ILA can be effectively modulated by HMGB1-TLR4 signalling. Consequently, administration of modulating ILA through HMGB1-TLR4 pathway may provide us more possibilities of treating inflammation and lymphangiogenesis associated diseases.

Indexed as

LymphangiogenesisSignal TransductionAnimalsBlotting, WesternCell LineCell ProliferationCells, CulturedEndothelial CellsEndothelium, LymphaticGene ExpressionHMGB1 ProteinInflammationInterleukin-1betaMacrophagesMaleMiceHMGB1 ProteinInterleukin-1betaToll-Like Receptor 4Tumor Necrosis Factor-alphaVascular Endothelial Growth Factor C

Identifiers

PMID27100831
PMCPMC4839690
OpenAlexW2340106508

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.