Evidence map›Paper›PMID 28953973›Full record

ArticlePloS one2017

Macroglia-derived thrombospondin 2 regulates alterations of presynaptic proteins of retinal neurons following elevated hydrostatic pressure.

Shuchao Wang, Tu Hu, Zhen Wang, Na Li, Lihong Zhou, Lvshuang Liao, Mi Wang, Libin Liao, Hui Wang, Leping Zeng and 5 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. A bibliometric analysis of apoptosis in glaucoma.Frontiers in neuroscience · 2023
    Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. 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

15 authors at 1 institution in 1 country.

Shuchao WangDepartment of Anatomy and Neurobiology, Central South University School of Basic Medical Sciences, Changsha, Hunan, China.
Tu HuDepartment of Anatomy and Neurobiology, Central South University School of Basic Medical Sciences, Changsha, Hunan, China.
Zhen WangDepartment of Anatomy and Neurobiology, Central South University School of Basic Medical Sciences, Changsha, Hunan, China.
Na LiDepartment of Anatomy and Neurobiology, Central South University School of Basic Medical Sciences, Changsha, Hunan, China.
Lihong ZhouDepartment of Anatomy and Neurobiology, Central South University School of Basic Medical Sciences, Changsha, Hunan, China.
Lvshuang LiaoDepartment of Anatomy and Neurobiology, Central South University School of Basic Medical Sciences, Changsha, Hunan, China.
Mi WangDepartment of Anatomy and Neurobiology, Central South University School of Basic Medical Sciences, Changsha, Hunan, China.
Libin LiaoDepartment of Anatomy and Neurobiology, Central South University School of Basic Medical Sciences, Changsha, Hunan, China.
Hui WangDepartment of Anatomy and Neurobiology, Central South University School of Basic Medical Sciences, Changsha, Hunan, China.
Leping ZengDepartment of Anatomy and Neurobiology, Central South University School of Basic Medical Sciences, Changsha, Hunan, China.
Chunling FanDepartment of Anatomy and Neurobiology, Central South University School of Basic Medical Sciences, Changsha, Hunan, China.
Hongkang ZhouDepartment of Anatomy and Neurobiology, Central South University School of Basic Medical Sciences, Changsha, Hunan, China.
Kun XiongDepartment of Anatomy and Neurobiology, Central South University School of Basic Medical Sciences, Changsha, Hunan, China.
Jufang HuangDepartment of Anatomy and Neurobiology, Central South University School of Basic Medical Sciences, Changsha, Hunan, China.
Dan ChenDepartment of Anatomy and Neurobiology, Central South University School of Basic Medical Sciences, Changsha, Hunan, China.ORCID http://orcid.org/0000-0002-2046-5986
Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many studies on retinal injury and repair following elevated intraocular pressure suggest that the survival ratio of retinal neurons has been improved by various measures. However, the visual function recovery is far lower than expected. The homeostasis of retinal synapses in the visual signal pathway is the key structural basis for the delivery of visual signals. Our previous studies found that complicated changes in the synaptic structure between retinal neurons occurred much earlier than obvious degeneration of retinal ganglion cells in rat retinae. The lack of consideration of these earlier retinal synaptic changes in the rescue strategy may be partly responsible for the limited visual function recovery with the types of protective methods for retinal neurons used following elevated intraocular pressure. Thus, research on the modulatory mechanisms of the synaptic changes after elevated intraocular pressure injury may give new light to visual function rescue. In this study, we found that thrombospondin 2, an important regulator of synaptogenesis in central nervous system development, was distributed in retinal macroglia cells, and its receptor α2δ-1 was in retinal neurons. Cell cultures including mixed retinal macroglia cells/neuron cultures and retinal neuron cultures were exposed to elevated hydrostatic pressure for 2 h. The expression levels of glial fibrillary acidic protein (the marker of activated macroglia cells), thrombospondin 2, α2δ-1 and presynaptic proteins were increased following elevated hydrostatic pressure in mixed cultures, but the expression levels of postsynaptic proteins were not changed. SiRNA targeting thrombospondin 2 could decrease the upregulation of presynaptic proteins induced by the elevated hydrostatic pressure. However, in retinal neuron cultures, elevated hydrostatic pressure did not affect the expression of presynaptic or postsynaptic proteins. Rather, the retinal neuron cultures with added recombinant thrombospondin 2 protein upregulated the level of presynaptic proteins. Finally, gabapentin decreased the expression of presynaptic proteins in mixed cultures by blocking the interaction of thrombospondin 2 and α2δ-1. Taken together, these results indicate that activated macroglia cells may participate in alterations of presynaptic proteins of retinal neurons following elevated hydrostatic pressure, and macroglia-derived thrombospondin 2 may modulate these changes via binding to its neuronal receptor α2δ-1.

Indexed as

Hydrostatic PressureAnimalsCalcium ChannelsCarrier ProteinsCells, CulturedDisks Large Homolog 4 ProteinGlial Fibrillary Acidic ProteinHomer Scaffolding ProteinsHumansIntracellular Signaling Peptides and ProteinsMembrane ProteinsNeurogliaPresynaptic TerminalsRats, Sprague-DawleyRetinal NeuronsSynapsinsCacna2d2 protein, ratCalcium ChannelsCarrier ProteinsDisks Large Homolog 4 ProteinDlg4 protein, ratgephyrinGlial Fibrillary Acidic ProteinHomer Scaffolding ProteinsIntracellular Signaling Peptides and ProteinsMembrane ProteinsSynapsinsSynaptophysinThrombospondin 2Thrombospondins

Identifiers

PMID28953973
PMCPMC5617560
OpenAlexW2758056943

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.