Evidence map›Paper›PMID 19941336›Full record

ArticleGlia2010

Cooperative induction of CXCL10 involves NADPH oxidase: Implications for HIV dementia.

Rachel Williams, Honghong Yao, Fuwang Peng, Yanjing Yang, Crystal Bethel-Brown, Shilpa Buch

Abstract read
In one paragraph

Article in Glia, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
5.2field-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

31 citing papers in PubMed, 53 citations in OpenAlex.

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  6. Drug discovery today. Disease models · 2020
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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 2 institutions in 1 country.

Rachel WilliamsDepartment of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, Kansas, USA.
Honghong Yao
Fuwang Peng
Yanjing Yang
Crystal Bethel-Brown
Shilpa Buch
Nebraska Medical Center · USUniversity of Kansas Medical Center · US

Funding

Morphine and the Neuropathogenesis of SIV in MacaquesR01DA024442 · NIDA · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BUCH, SHILPA J. · 2007 to 2011
$2.8M
Mechanism and Therapy of SHIV Encephalitis in MacaquesR01MH068212 · NIMH · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BUCH, SHILPA J. · 2003 to 2012
$2.7M
HIV-Encephalitis and Cocaine Abuse: Mechanism of Synergy and TherapyR01DA020392 · NIDA · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BUCH, SHILPA J. · 2006 to 2010
$1.4M
PLGA/Antisense IL-10: Gene Therapy for Cocaine Abusers with HADR21DA023397 · NIDA · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BUCH, SHILPA J. · 2009 to 2010
$423k
HIV-Encephalitis: Mechanisms for CXCL 10 Induction in AstrocytesF31NS062665 · NINDS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI WILLIAMS, RACHEL · 2008 to 2009
$32k
NIDA NIH HHS DA020392NIDA NIH HHS DA023397NIDA NIH HHS DA024442NIDA NIH HHS R01 DA020392NIDA NIH HHS R01 DA024442NIDA NIH HHS R21 DA023397NIMH NIH HHS MH-068212NIMH NIH HHS R01 MH068212NINDS NIH HHS F31 NS062665NINDS NIH HHS F31NS062665
6 · The paper itself

Abstract

With the increasing prevalence of HIV-associated neurocognititve disorders (HAND), understanding the mechanisms by which HIV-1 induces neuro-inflammation and subsequent neuronal damage is important. The hallmark features of HIV-encephalitis, the pathological correlate of HIV-associated Dementia (HAD), are gliosis, oxidative stress, chemokine dysregulation, and neuronal damage/death. Since neurons are not infected by HIV-1, the current thinking is that these cells are damaged indirectly by pro-inflammatory chemokines released by activated glial cells. CXCL10 is a neurotoxic chemokine that is upregulated in astroglia activated by HIV-1 Tat, IFN-gamma, and TNF-alpha. In this study we have demonstrated that HIV-1 Tat increases CXCL10 expression in IFN-gamma and TNF-alpha stimulated human astrocytes via NADPH oxidase. We have shown that the treatment of astrocytes with a mixture of Tat and cytokines leads to a respiratory burst that is abrogated by apocynin, an NADPH oxidase inhibitor. Pretreatment of Tat, IFN-gamma, and TNF-alpha stimulated astrocytes with apocynin also resulted in concomitant inhibition of CXCL10 expression. Additionally, apocynin was also able to reduce Tat and cytokine-mediated activation of the corresponding signaling molecules Erk1/2, Jnk, and Akt with a decrease in activation and nuclear translocation of NF-kappaB, important regulators of CXCL10 induction. Understanding the mechanisms involved in reducing both oxidative stress and the release of pro-inflammatory agents could lead to the development of therapeutics aimed at decreasing neuro-inflammation in patients suffering from HAD.

Indexed as

AcetophenonesAstrocytesCell Line, TransformedChemokine CXCL10Drug InteractionsEnzyme InhibitorsEnzyme-Linked Immunosorbent AssayExtracellular Signal-Regulated MAP KinasesGene Expression Regulation, EnzymologicHumansInterferon-alphaInterferon-gammaMembrane GlycoproteinsNADPH Oxidase 2NADPH OxidasesOxidative StressAcetophenonesacetovanilloneChemokine CXCL10CYBB protein, humanEnzyme InhibitorsExtracellular Signal-Regulated MAP KinasesInterferon-alphaInterferon-gammaMembrane GlycoproteinsNADPH Oxidase 2NADPH OxidasesRNA, Small Interferingtat Gene Products, Human Immunodeficiency Virus

Identifiers

PMID19941336
PMCPMC2820595
OpenAlexW2021061796

What OpenQuestion 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 OpenQuestion graph.