Evidence map›Paper›PMID 14685691›Full record

ArticleCellular and molecular life sciences : CMLS2003

Neuronal thread protein regulation and interaction with microtubule-associated proteins in SH-Sy5y neuronal cells.

S M de la Monte, G J Chen, E Rivera, J R Wands

Open access · greenAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

24 citing papers in PubMed, 44 citations in OpenAlex.

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  14. Linking insulin with Alzheimer's disease: emergence as type III diabetes.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2015
    Review
  15. Type 3 diabetes is sporadic Alzheimer׳s disease: mini-review.European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology · 2014
    Review
  16. Review
  17. Review
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  19. Role of central nervous system insulin resistance in fetal alcohol spectrum disorders.Journal of population therapeutics and clinical pharmacology = Journal de la therapeutique des populations et de la pharmacologie clinique · 2010
    Review
  20. Alzheimer's disease is type 3 diabetes-evidence reviewed.Journal of diabetes science and technology · 2008
    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 2 institutions in 1 country.

S M de la MonteDepartment of Medicine, Rhode Island Hospital and Brown Medical School, 55 Claverick Street, Providence, Rhode Island 02903, USA. suzannedelamontemd@brown.edu
G J Chen
E Rivera
J R Wands
Providence College · USRhode Island Hospital · US

Funding

WNT SIGNALING IN HEPATOCELLULAR CARCINOMAP20RR015578 · NCRR · BROWN UNIVERSITY · PI JOGL, GERWALD · 2000 to 2009
$22.8M
EFFECTS OF ALCOHOL ON THE LIVERR01AA002666 · NIAAA · RHODE ISLAND HOSPITAL (PROVIDENCE, RI) · PI WANDS, JACK R · 1985 to 2007
$2.6M
EFFECTS OF ALCOHOL ON THE LIVERR37AA002666 · NIAAA · MASSACHUSETTS GENERAL HOSPITAL · PI WANDS, JACK R · 1989 to 1997
–
NCRR NIH HHS P20RR15578NIAAA NIH HHS AA02666NIAAA NIH HHS AA11931NIAAA NIH HHS AA12458
6 · The paper itself

Abstract

In Alzheimer's disease (AD), neuronal thread protein (NTP) accumulates in cortical neurons and colocalizes with phospho- tau-immunoreactive cytoskeletal lesions that correlate with dementia. To generate additional information about the potential role of NTP in AD, we characterized its expression and regulation in human SH-Sy5y neuronal cells. Quantitative real-time reverse transcription-polymerase chain reactin and Western blot analysis demonstrated prominent insulin, moderate insulin-like growth factor, type 1 (IGF-1) and minimal nerve growth factor stimulation of NTP expression. In addition, NTP protein was more stable and it progressively accumulated in cells that were stimulated with insulin for 24 or 48 h. Metabolic labeling and phospho-amino acid analysis demonstrated phosphorylation of NTP on Serine residues, 30-60 min after insulin or IGF-1 stimulation, when glycogen synthase kinase 3beta (GSK-3beta) activity would no longer have been suppressed. Kinase inhibitor and in vitro phosphorylation studies demonstrated a role for GSK-3beta in the positive regulation of NTP expression and phosphorylation. Coimmunoprecipitation studies demonstrated physical interactions between NTP and tau or microtubule-associated protein 1b (MAP-1b), and ubiquitin immunoreactivity in NTP immunoprecipitates. In summary, these studies showed that (i) NTP expression is regulated at the level of transcription by insulin and IGF-1 stimulation; (ii) NTP is phosphorylated by GSK-3beta; (iii) NTP can physically interact with tau and MAP-1b and (iv) NTP-MAP complexes are ubiquitinated. The results suggest a functional role for NTP in relation to the turnover or processing of neuronal cytoskeletal proteins, attributes that may be modulated by insulin/IGF-1-mediated signaling.

Indexed as

Nerve Tissue ProteinsAntibodies, MonoclonalBrainCalcium-Binding ProteinsHumansInsulinLithostathineMicrotubule-Associated ProteinsMicrotubulesNeuronsPhosphorylationPhosphotransferasesSignal Transductiontau ProteinsAD7c-NTP protein, humanAntibodies, MonoclonalCalcium-Binding ProteinsInsulinLithostathinemicrotubule-associated protein 1BMicrotubule-Associated ProteinsNerve Tissue ProteinsPhosphotransferasestau Proteins

Identifiers

PMID14685691
PMCPMC11138531
OpenAlexW2043345148

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.