Evidence map›Paper›PMID 11161609›Full record

ArticleExperimental neurology2001

Response of cell cycle proteins to neurotrophic factor and chemokine stimulation in human neuroglia.

K L Jordan-Sciutto, B A Murray Fenner, C A Wiley, C L Achim

Abstract read
In one paragraph

Article in Experimental neurology, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

11 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Review
  3. Chemotactic and mitogenic stimuli of neuronal apoptosis in patients with medically intractable temporal lobe epilepsy.Pathophysiology : the official journal of the International Society for Pathophysiology · 2013
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Altered distribution of cell cycle transcriptional regulators during Alzheimer disease.Journal of neuropathology and experimental neurology · 2002
    Article
  11. Cell cycle proteins exhibit altered expression patterns in lentiviral-associated encephalitis.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2002
    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

4 authors at 1 institution in 1 country.

K L Jordan-SciuttoDepartment of Pathology, Division of Neuropathology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15213, USA. jordan@np.awing.upmc.edu
B A Murray Fenner
C A Wiley
C L Achim
University of Pittsburgh · US

Funding

ROLE OF CELL CYCLE PROTEINS IN HIV ENCEPHALITISR01NS041202 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI JORDAN-SCIUTTO, KELLY L · 2001 to 2015
$4.5M
AIDS BRAIN MACROPHAGES--VIRAL SPREAD AND NEUROTOXICITYR01MH058528 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ACHIM, CRISTIAN L · 1998 to 2003
$786k
MOLECULAR MECHANISMS OF BRAIN DEVELOPMENT AND DISEASEF32NS010572 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI JORDAN-SCIUTTO, KELLY L · 1997 to 1998
–
NEUROTROPHIC FACTORS IN HIV ENCEPHALITISR01NS035731 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WILEY, CLAYTON A. · 1996 to 1999
–
NIMH NIH HHS MH 58528NINDS NIH HHS F32 NS010572NINDS NIH HHS NS10572NINDS NIH HHS NS 35731NINDS NIH HHS R01 NS041202
6 · The paper itself

Abstract

Increased expression of neurotrophins (e.g., NGF, BDNF) and chemokines (e.g., RANTES) has been observed in neurodegenerative diseases. We examined the effect of these factors on intracellular signaling cascades inducing cell cycle proteins p53, pRb, and E2F1 in human fetal mixed neuronal and glial cells. Comparing neurotrophin- and chemokine-treated cultures with untreated controls showed altered subcellular localization and expression of hyperphosphorylated retinoblastoma protein (ppRb), E2F1, and p53. Using immunofluorescent laser confocal microscopy, E2F1 and ppRb were detected exclusively in neuronal nuclei in control cultures while p53 was cytoplasmic in astrocytes and nuclear in neurons. Following treatment with neurotrophins, E2F1 and ppRb were observed in the cytoplasm of neurons, while p53 was observed in both neuronal and astrocytic nuclei. Similar findings were observed following treatment with RANTES. Semiquantitative analysis using immunoblots showed an increase in the amount of phosphorylated pRb in treated cultures. Induction of cell cycle proteins may play a role in neurodegeneration associated with neurotrophin and chemokine stimulation.

Indexed as

Carrier ProteinsDNA-Binding ProteinsAstrocytesBrain-Derived Neurotrophic FactorCell Cycle ProteinsCell NucleusCells, CulturedChemokine CCL5ChemokinesCytoplasmE2F1 Transcription FactorE2F Transcription FactorsHumansNerve Growth FactorNerve Growth FactorsNeurogliaBrain-Derived Neurotrophic FactorCarrier ProteinsCell Cycle ProteinsChemokine CCL5ChemokinesDNA-Binding ProteinsE2F1 protein, humanE2F1 Transcription FactorE2F Transcription FactorsNerve Growth FactorNerve Growth FactorsRetinoblastoma-Binding Protein 1Retinoblastoma ProteinTranscription Factor DP1Transcription FactorsTumor Suppressor Protein p53

Identifiers

PMID11161609
PMCPMC3683587
OpenAlexW2124093647

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.