Evidence map›Paper›PMID 28402693›Full record

ArticleAutophagy2017

Heparan sulfate proteoglycans regulate autophagy in Drosophila.

Claire E Reynolds-Peterson, Na Zhao, Jie Xu, Taryn M Serman, Jielin Xu, Scott B Selleck

Open access · bronzeAbstract read
In one paragraph

Article in Autophagy, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 31% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
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  5. Article
  6. Review
  7. Review
  8. A functional outside-in signaling network of proteoglycans and matrix molecules regulating autophagy.Matrix biology : journal of the International Society for Matrix Biology · 2021
    Article
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  10. 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

6 authors at 1 institution in 1 country.

Claire E Reynolds-Petersona Department of Biochemistry and Molecular Biology , The Pennsylvania State University , University Park , PA , USA.
Na Zhaoa Department of Biochemistry and Molecular Biology , The Pennsylvania State University , University Park , PA , USA.
Jie Xua Department of Biochemistry and Molecular Biology , The Pennsylvania State University , University Park , PA , USA.
Taryn M Sermana Department of Biochemistry and Molecular Biology , The Pennsylvania State University , University Park , PA , USA.
Jielin Xua Department of Biochemistry and Molecular Biology , The Pennsylvania State University , University Park , PA , USA.
Scott B Sellecka Department of Biochemistry and Molecular Biology , The Pennsylvania State University , University Park , PA , USA.
Pennsylvania State University · US

Funding

PROTEOGLYCANS IN GROWTH FACTOR SIGNALING AND DEVELOPMENTR01GM054832 · NIGMS · UNIVERSITY OF MINNESOTA TWIN CITIES · PI SELLECK, SCOTT B · 1997 to 2010
$2.4M
NIGMS NIH HHS R01 GM054832
6 · The paper itself

Abstract

Heparan sulfate-modified proteoglycans (HSPGs) are important regulators of signaling and molecular recognition at the cell surface and in the extracellular space. Disruption of HSPG core proteins, HS-synthesis, or HS-degradation can have profound effects on growth, patterning, and cell survival. The Drosophila neuromuscular junction provides a tractable model for understanding the activities of HSPGs at a synapse that displays developmental and activity-dependent plasticity. Muscle cell-specific knockdown of HS biosynthesis disrupted the organization of a specialized postsynaptic membrane, the subsynaptic reticulum (SSR), and affected the number and morphology of mitochondria. We provide evidence that these changes result from a dysregulation of macroautophagy (hereafter referred to as autophagy). Cellular and molecular markers of autophagy are all consistent with an increase in the levels of autophagy in the absence of normal HS-chain biosynthesis and modification. HS production is also required for normal levels of autophagy in the fat body, the central energy storage and nutritional sensing organ in Drosophila. Genetic mosaic analysis indicates that HS-dependent regulation of autophagy occurs non-cell autonomously, consistent with HSPGs influencing this cellular process via signaling in the extracellular space. These findings demonstrate that HS biosynthesis has important regulatory effects on autophagy and that autophagy is critical for normal assembly of postsynaptic membrane specializations.

Indexed as

AutophagyAnimalsAutophagosomesAutophagy-Related ProteinsDown-RegulationDrosophilaDrosophila melanogasterFat BodyHeparan Sulfate ProteoglycansHomozygoteLarvaMitochondriaMusclesMutationNeuromuscular JunctionPhenotypeAutophagy-Related ProteinsHeparan Sulfate ProteoglycansautophagyDrosophilaheparan sulfate proteoglycanmitochondriasubsynaptic reticulum

Identifiers

PMID28402693
PMCPMC5584867
OpenAlexW2606044352

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.