Evidence map›Paper›PMID 18588860›Full record

ArticleBrain research2008

Brain-derived neurotrophic factor modulates expression of chemokine receptors in the brain.

Farid Ahmed, Lino Tessarollo, Carol Thiele, Italo Mocchetti

Abstract read
In one paragraph

Article in Brain research, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
0.9field-weighted citation impact, top 29% 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

20 citing papers in PubMed, 34 citations in OpenAlex.

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  11. Implementing neuronal plasticity in NeuroAIDS: the experience of brain-derived neurotrophic factor and other neurotrophic factors.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2014
    Review
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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

4 authors at 3 institutions in 1 country.

Farid AhmedDepartment of Neuroscience, Georgetown University Medical Center, Washington DC, USA.
Lino Tessarollo
Carol Thiele
Italo Mocchetti
National Cancer Institute · USGeorgetown University · USGeorgetown University Medical Center · US

Funding

Role of Neurotrophins in the Development of the Mammalian Nervous SystemZIABC010390 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI TESSAROLLO, LINO · 2009 to 2025
$14.2M
Neurotrophic factors and HIV-mediated neuronal injuryR01NS040670 · NINDS · GEORGETOWN UNIVERSITY · PI MOCCHETTI, ITALO · 2001 to 2008
$2.3M
Pathophysiologic Consequences of Neurotrophin Activation of Trk in NeuroblastomaZ01BC010789 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI THIELE, CAROL J · 2007 to 2008
$1.1M
Role of Trk Receptors in the Development and Function of Non-neuronal StructuresZ01BC010391 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI TESSAROLLO, LINO · 2000 to 2008
$1.1M
Intramural NIH HHSNINDS NIH HHS NS 040670NINDS NIH HHS R01 NS040670
6 · The paper itself

Abstract

Chemokine receptors, and in particular CXCR4 and CCR5 play a key role in the neuropathogenesis of Human Immunodeficiency Virus-1 (HIV)4 associated dementia (HAD). Thus, new insight into the expression of CXCR4 in the central nervous system may help develop therapeutic compounds against HAD. Brain-derived neurotrophic factor (BDNF) is neuroprotective in vitro against two strains of the HIV envelope protein gp120 that binds to CXCR4 or CCR5. Therefore, we examined whether BDNF modulates chemokine receptor expression in vivo. The content of CXCR4 mRNA and proteins was determined in the cerebral cortex and hippocampus of 6-month-old BDNF heterozygous mice and wild type littermates by using polymerase chain reaction and immunohistochemistry, respectively. BDNF heterozygous mice exhibited an increase in CXCR4 mRNA compared to wild type. Histological analyses revealed an up-regulation of CXCR4 immunoreactivity mainly in neurons. Most of these neurons were positive for TrkB, the BDNF receptor with a tyrosine kinase activity. Increases in CXCR4 mRNA levels were observed in 18-month-old BDNF heterozygous mice but not in 7-day-old mice, suggesting that the modulatory role of BDNF occurs only in mature animals. To determine whether BDNF affects also CXCR4 internalization, SH-SY5Y neuroblastoma cells were exposed to BDNF and cell surface CXCR4 levels were measured at various times. BDNF induced CXCR4 internalization within minutes. Lastly, BDNF heterozygous mice showed higher levels of CCR5 and CXCR3 mRNA than wild type in the cerebral cortex, hippocampus and striatum. Our data indicate that BDNF may modulate the availability of chemokine receptors implicated in HIV infection.

Indexed as

AnimalsBrainBrain-Derived Neurotrophic FactorCell Line, TumorCerebral CortexCorpus StriatumCyclophilinsFluorescent Antibody Technique, DirectGlial Fibrillary Acidic ProteinHeterozygoteHippocampusHumansImmunohistochemistryMiceMice, Inbred C57BLMice, KnockoutBrain-Derived Neurotrophic FactorCyclophilinsGlial Fibrillary Acidic ProteinReceptors, CCR5Receptors, ChemokineReceptors, CXCR3Receptors, CXCR4Receptor, trkBRibosomal ProteinsRNA, MessengerRpl19 protein, mouse

Identifiers

PMID18588860
PMCPMC2601566
OpenAlexW2079253012

What OpenQuestion holds

Textmetadata
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.