Evidence map›Paper›PMID 27003822›Full record

ArticleMolecular neurobiology2017

NCAM-140 Translocation into Lipid Rafts Mediates the Neuroprotective Effects of GDNF.

Li Li, Huizhen Chen, Meng Wang, Fangfang Chen, Jin Gao, Shen Sun, Yunqing Li, Dianshuai Gao

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular neurobiology, 2017. 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
1.0field-weighted citation impact, top 27% 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, 19 citations in OpenAlex.

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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

8 authors at 4 institutions in 1 country.

Li LiDepartment of Pathophysiology, Xuzhou Medical College, Xuzhou, China.
Huizhen ChenDepartment of Neurobiology and Human Anatomy, Xuzhou Medical College, Tongshan Road No. 209, Xuzhou, 221002, China.
Meng WangDepartment of Neurobiology and Human Anatomy, Xuzhou Medical College, Tongshan Road No. 209, Xuzhou, 221002, China.
Fangfang ChenDepartment of Neurobiology and Human Anatomy, Xuzhou Medical College, Tongshan Road No. 209, Xuzhou, 221002, China.
Jin GaoDepartment of Neurobiology and Human Anatomy, Xuzhou Medical College, Tongshan Road No. 209, Xuzhou, 221002, China.
Shen SunDepartment of Neurobiology and Human Anatomy, Xuzhou Medical College, Tongshan Road No. 209, Xuzhou, 221002, China.
Yunqing LiDepartment of Human Anatomy, Histology and Embryology, School of the Basic Medicine, The Fourth Military Medical University, Xi'an, China.
Dianshuai GaoDepartment of Neurobiology and Human Anatomy, Xuzhou Medical College, Tongshan Road No. 209, Xuzhou, 221002, China. dshgao@vip.sina.com.
Xuzhou Medical College · CNAir Force Medical University · CNChina Pharmaceutical University · CNThe First People’s Hospital of Lianyungang · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glial cell line-derived neurotrophic factor (GDNF) is a potent neurotrophic factor for substantia nigra dopaminergic (DA) neuronal cells. Recent studies have demonstrated that neural cell adhesion molecule functions as a signal transduction receptor for GDNF. The purpose of this study is to reveal whether neural cell adhesion molecule (NCAM) mediates the protective effects of GDNF on DA neuronal cells and further explore the mechanisms involved. We utilized SH-SY5Y cell line to establish a model of 6-hydroxydopamine (6-OHDA)-injured DA neuronal cells. Lentiviral vectors were constructed to knockdown or overexpress NCAM-140, and a density gradient centrifugation method was employed to separate membrane lipid rafts. 3-(4,5-Dimethythiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT), flow cytometric analysis, and western blotting were used to evaluate the protective effects of GDNF. The results showed that GDNF could protect 6-OHDA-injured SH-SY5Y cells via improving cell viability and decreasing the cell death rate and cleaved caspase-3 expression. NCAM-140 knockdown decreased cell viability and increased the cell death rate and cleaved caspase-3 expression, while its overexpression had the opposite effects. Notably, the amount of NCAM-140 located in lipid rafts increased after GDNF treatment. Pretreatment with 2-bromopalmitate, a specific inhibitor of protein palmitoylation, suppressed NCAM-140 translocation to lipid rafts and reduced the NCAM-mediated protective effects of GDNF on injured DA neuronal cells. Our results suggest that GDNF have the protective effects on injured DA cells by influencing NCAM-140 translocation into lipid rafts.

Indexed as

Caspase 3CD56 AntigenCell DeathCell Line, TumorCell SurvivalGene Knockdown TechniquesGenetic VectorsGlial Cell Line-Derived Neurotrophic FactorHumansLentivirusMembrane MicrodomainsMicroscopy, FluorescenceNeuroblastomaNeuroprotective AgentsPalmitatesProtein Isoforms2-bromopalmitateCaspase 3CD56 AntigenGlial Cell Line-Derived Neurotrophic FactorNCAM1 protein, humanNeuroprotective AgentsPalmitatesProtein IsoformsRNA, Small InterferingDopaminergic neuronal cellsGlial cell line-derived neurotrophic factorLipid raftsNeural cell adhesion moleculeParkinson’s disease

Identifiers

PMID27003822
OpenAlexW2303974212

What OpenQuestion holds

Textmetadata
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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.