Evidence map›Paper›PMID 30380410›Full record

ArticleCell reports2018

Transcriptional Regulation of Lipophorin Receptors Supports Neuronal Adaptation to Chronic Elevations of Activity.

Jun Yin, Mary Gibbs, Caixia Long, Justin Rosenthal, Hyong S Kim, Anna Kim, Chengyu Sheng, Peng Ding, Uzma Javed, Quan Yuan

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

9 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
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  6. Temporal regulation of nicotinic acetylcholine receptor subunits supports central cholinergic synapse development inProceedings of the National Academy of Sciences of the United States of America · 2021
    Article
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  8. 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

10 authors at 2 institutions in 1 country.

Jun YinDendrite Morphogenesis and Plasticity Unit, National Institute of Neurological Disorders and Stroke, NIH, Bethesda, MD 20892, USA.
Mary GibbsDendrite Morphogenesis and Plasticity Unit, National Institute of Neurological Disorders and Stroke, NIH, Bethesda, MD 20892, USA.
Caixia LongDendrite Morphogenesis and Plasticity Unit, National Institute of Neurological Disorders and Stroke, NIH, Bethesda, MD 20892, USA.
Justin RosenthalDendrite Morphogenesis and Plasticity Unit, National Institute of Neurological Disorders and Stroke, NIH, Bethesda, MD 20892, USA.
Hyong S KimDendrite Morphogenesis and Plasticity Unit, National Institute of Neurological Disorders and Stroke, NIH, Bethesda, MD 20892, USA.
Anna KimDendrite Morphogenesis and Plasticity Unit, National Institute of Neurological Disorders and Stroke, NIH, Bethesda, MD 20892, USA.
Chengyu ShengDendrite Morphogenesis and Plasticity Unit, National Institute of Neurological Disorders and Stroke, NIH, Bethesda, MD 20892, USA.
Peng DingNeurobiology Department, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Uzma JavedDendrite Morphogenesis and Plasticity Unit, National Institute of Neurological Disorders and Stroke, NIH, Bethesda, MD 20892, USA.
Quan YuanDendrite Morphogenesis and Plasticity Unit, National Institute of Neurological Disorders and Stroke, NIH, Bethesda, MD 20892, USA. Electronic address: quan.yuan@nih.gov.
Morpho (United States) · USUniversity of Massachusetts Chan Medical School · US

Funding

Study dendrite morphogenesis and activity-dependent plasticity using DrosophilaZIANS003137 · NINDS · NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE · PI YUAN, QUAN · 2013 to 2025
$24.9M
Intramural NIH HHS ZIA NS003137
6 · The paper itself

Abstract

Activity-dependent modifications strongly influence neural development. However, molecular programs underlying their context and circuit-specific effects are not well understood. To study global transcriptional changes associated with chronic elevation of synaptic activity, we performed cell-type-specific transcriptome profiling of Drosophila ventral lateral neurons (LNvs) in the developing visual circuit and identified activity-modified transcripts that are enriched in neuron morphogenesis, circadian regulation, and lipid metabolism and trafficking. Using bioinformatics and genetic analyses, we validated activity-induced isoform-specific upregulation of Drosophila lipophorin receptors LpR1 and LpR2, the homologs of mammalian low-density lipoprotein receptor (LDLR) family proteins. Furthermore, our morphological and physiological studies uncovered critical functions of neuronal lipophorin receptors (LpRs) in maintaining the structural and functional integrities in neurons challenged by chronic elevations of activity. Together, our findings identify LpRs as molecular targets for activity-dependent transcriptional regulation and reveal the functional significance of cell-type-specific regulation of neuronal lipid uptake in experience-dependent plasticity and adaptive responses.

Indexed as

Gene Expression RegulationTranscription, GeneticAdaptation, PhysiologicalAnimalsDendritesDrosophila melanogasterDrosophila ProteinsMorphogenesisNeuronsReceptors, Cytoplasmic and NuclearRNA InterferenceRNA, MessengerTranscriptomeUp-RegulationDrosophila ProteinsLpr1 protein, DrosophilaLpr2 protein, DrosophilaReceptors, Cytoplasmic and NuclearRNA, Messengeractivity-dependent transcriptional regulationdendrite morphogenesislipid homeostasislipid uptakelipoprotein receptorneural developmentneuronal adaptationRNA-seq analysisstructural plasticitytranscriptome profiling

Identifiers

PMID30380410
PMCPMC6294312
OpenAlexW2899359772

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.