Evidence map›Paper›PMID 24026137›Full record

ArticleCytokine2013

Norepinephrine and adenosine-5'-triphosphate synergize in inducing IL-6 production by human dermal microvascular endothelial cells.

Lori L Stohl, Julie B Zang, Wanhong Ding, Michela Manni, Xi K Zhou, Richard D Granstein

Open access · greenAbstract read
In one paragraph

Article in Cytokine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.6field-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

23 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Faricimab Reverts VEGF-AInternational journal of molecular sciences · 2025
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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

6 authors at 1 institution in 1 country.

Lori L StohlDepartment of Dermatology, Weill Cornell Medical College, 1305 York Avenue, 9th Floor, New York, NY 10021, United States.
Julie B Zang
Wanhong Ding
Michela Manni
Xi K Zhou
Richard D Granstein
Cornell University · US

Funding

CTSA INFRASTRUCTURE FOR PEDIATRIC RESEARCHUL1RR024996 · NCRR · WEILL MEDICAL COLL OF CORNELL UNIV · PI IMPERATO-MCGINLEY, JULIANNE L · 2007 to 2011
$49.6M
Clinical and Translational Science CenterUL1TR000457 · NCATS · WEILL MEDICAL COLL OF CORNELL UNIV · PI IMPERATO-MCGINLEY, JULIANNE L · 2012 to 2016
$46.0M
REGULATION OF LANGERHANS CELL FUNCTION BY CGRPR01AR042429 · NIAMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI GRANSTEIN, RICHARD DAVID · 1994 to 2009
$2.8M
NCATS NIH HHS UL1 TR000457NCRR NIH HHS UL1 RR024996NIAMS NIH HHS R01 AR042429NIAMS NIH HHS R01 AR42429
6 · The paper itself

Abstract

Endothelial cells (ECs) play important roles in cutaneous inflammation, in part, by release of inflammatory chemokines/cytokines. Because dermal blood vessels are innervated by sympathetic nerves, the sympathetic neurotransmitter norepinephrine (NE) and the co-transmitter adenosine-5'-triphosphate (ATP) may regulate expression of EC inflammatory factors. We focused on IL-6 regulation because it has many inflammatory and immune functions, including participation in Th17 cell differentiation. Strikingly, NE and ATP synergistically induced release of IL-6 by a human dermal microvascular endothelial cell line (HMEC-1). Adrenergic antagonist and agonist studies indicated that the effect of NE on induced IL-6 release is primarily mediated by β2-adrenergic receptors (ARs). By real-time PCR IL-6 mRNA was also synergistically induced in HMEC-1 cells. This synergistic effect of NE and ATP was reproduced in primary human dermal endothelial cells (pHDMECs) and is also primarily mediated by β2-ARs. Under conditions of stress, activation of the symphathetic nervous system may lead to release of ATP and NE by sympathetic nerves surrounding dermal blood vessels with induction of IL-6 production by ECs. IL-6 may then participate in immune and inflammatory processes including generation of Th17 cells. Production of IL-6 in this manner might explain stress-induced exacerbation of psoriasis, and perhaps, other skin disorders involving Th17-type immunity.

Indexed as

Adenosine TriphosphateAdrenergic beta-2 Receptor AgonistsAdrenergic beta-2 Receptor AntagonistsCell CountCell LineCell SurvivalDermisEndothelial CellsGene Expression RegulationHumansInterleukin-6MicrovesselsNorepinephrineReal-Time Polymerase Chain ReactionReceptors, Adrenergic, beta-2RNA, MessengerAdenosine TriphosphateAdrenergic beta-2 Receptor AgonistsAdrenergic beta-2 Receptor AntagonistsIL6 protein, humanInterleukin-6NorepinephrineReceptors, Adrenergic, beta-2RNA, Messengeradenosine-5′-triphosphateAdenosine-5′-triphosphateadrenergic receptorARATPdepleted mediumDMECendothelial cellEndothelial cellsICAM-1IL-6intercellular adhesion molecule 1NEnorepinephrineNorepinephrinepHDMECprimary human dermal endothelial cellsProppropranololSalsalbutamolSNSsympathetic nervous system

Identifiers

PMID24026137
PMCPMC3835662
OpenAlexW2043041195

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.