Evidence map›Paper›PMID 33986920›Full record

ArticleScience signaling2021

Endothelial TLR2 promotes proangiogenic immune cell recruitment and tumor angiogenesis.

Michael G McCoy, Daniel W Nascimento, Manoj Veleeparambil, Rakhylia Murtazina, Detao Gao, Svyatoslav Tkachenko, Eugene Podrez, Tatiana V Byzova

Open access · greenAbstract read
In one paragraph

Article in Science signaling, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

32 citing papers in PubMed, 53 citations in OpenAlex.

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  10. Role of Innate Immunity in Cancer.Advances in experimental medicine and biology · 2025
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Michael G McCoyDepartment of Neuroscience, Lerner Research Institute, Cleveland Clinic, OH, USA 44195.
Daniel W NascimentoDepartment of Neuroscience, Lerner Research Institute, Cleveland Clinic, OH, USA 44195.
Manoj VeleeparambilDepartment of Neuroscience, Lerner Research Institute, Cleveland Clinic, OH, USA 44195.
Rakhylia MurtazinaDepartment of Neuroscience, Lerner Research Institute, Cleveland Clinic, OH, USA 44195.
Detao GaoDepartment of Inflammation and Immunity, Lerner Research Institute, Cleveland Clinic, OH, USA 44195.
Svyatoslav TkachenkoDepartment of Quantitative Health Sciences, Lerner Research Institute, Cleveland Clinic, OH, USA 44195.
Eugene PodrezDepartment of Inflammation and Immunity, Lerner Research Institute, Cleveland Clinic, OH, USA 44195.
Tatiana V ByzovaDepartment of Neuroscience, Lerner Research Institute, Cleveland Clinic, OH, USA 44195.
Cleveland Clinic Lerner College of Medicine · US

Funding

Regulation of Integrins in Neovasculature DevelopmentR01HL071625 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI BYZOVA, TATIANA V · 2003 to 2021
$7.3M
Role of TLR2 in angiogenesisR01HL145536 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI BYZOVA, TATIANA V · 2019 to 2022
$2.6M
Spinning Disk Confocoal MicroscopeS10RR026820 · NCRR · CLEVELAND CLINIC LERNER COM-CWRU · PI DRAZBA, JUDY · 2010 to 2010
$500k
NCRR NIH HHS S10 RR026820NHLBI NIH HHS R01 HL071625NHLBI NIH HHS R01 HL145536
6 · The paper itself

Abstract

Toll-like receptor 2 (TLR2) is implicated in various pathologies, mainly in terms of its function within innate immune cells. However, TLR2 is also present in endothelial cells. Here, we explored the physiological and pathophysiological roles of endothelial TLR2 signaling. We found that TLR2 was highly abundant in the endothelium within various tissues using TLR2-IRES-EGFP reporter mice and was required for proinflammatory endothelial cell function. Endothelial cells lacking TLR2 exhibited reduced proinflammatory potential at the protein, cell, and tissue levels. Loss of endothelial TLR2 blunted the inflammatory response to both exogenous and endogenous danger signals in endothelial cells in culture and in vivo. Endothelial TLR2 promoted tumor growth, angiogenesis, and protumorigenic immune cell recruitment in a mouse model of prostate cancer. Furthermore, the cell surface localization of P-selectin and the subsequent production of other critical cell adhesion molecules (such as E-selectin, ICAM-1 and VCAM-1) that recruit immune cells required endothelial TLR2. Our findings demonstrate that endothelial cells actively contribute to innate immune pathways and propose that endothelial TLR2 has a pathological role in proinflammatory conditions.

Indexed as

Neovascularization, PathologicSignal TransductionAnimalsEndotheliumInflammationMaleMiceProstatic NeoplasmsP-SelectinToll-Like Receptor 2P-SelectinTlr2 protein, mouseToll-Like Receptor 2

Identifiers

PMID33986920
PMCPMC8112454
OpenAlexW3125482080

What OpenQuestion holds

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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.