Evidence map›Paper›PMID 30191418›Full record

ArticleJapanese journal of ophthalmology2018

Infection of endotheliotropic human cytomegalovirus of trabecular meshwork cells.

Daisuke Shimizu, Dai Miyazaki, Yumiko Shimizu, Mayumi Hosogai, Isao Kosugi, Yoshitsugu Inoue

Open access · bronzeAbstract read
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In one paragraph

Article in Japanese journal of ophthalmology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

15 citing papers in PubMed, 16 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Management of cytomegalovirus corneal endotheliitis.Eye and vision (London, England) · 2021
    Review
  13. Article
  14. Article
  15. Diagnostic efficacy of real-time PCR for ocular cytomegalovirus infections.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2018
    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

6 authors at 4 institutions in 1 country.

Daisuke ShimizuDepartment of Ophthalmology and Visual Science, Tottori University Faculty of Medicine, 36-1 Nishicho, Yonago, 683-8504, Japan.
Dai MiyazakiDepartment of Ophthalmology and Visual Science, Tottori University Faculty of Medicine, 36-1 Nishicho, Yonago, 683-8504, Japan. miyazaki-ttr@umin.ac.jp.
Yumiko ShimizuDepartment of Ophthalmology and Visual Science, Tottori University Faculty of Medicine, 36-1 Nishicho, Yonago, 683-8504, Japan.
Mayumi HosogaiDepartment of Ophthalmology, Gunma University Graduate School of Medicine, Maebashi, Japan.
Isao KosugiDepartment of Regenerative and Infectious Pathology, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Yoshitsugu InoueDepartment of Ophthalmology and Visual Science, Tottori University Faculty of Medicine, 36-1 Nishicho, Yonago, 683-8504, Japan.
Tottori University · JPChiba University · JPGunma University · JPHamamatsu University School of Medicine · JP

Funding

Scientific Research from the Japanese Ministry of Education, Science, and Culture 16K11322Scientific Research from the Japanese Ministry of Education, Science, and Culture 17K11481Scientific Research from the Japanese Ministry of Education, Science, and Culture 17K16969
6 · The paper itself

Abstract

purposeHuman cytomegalovirus (HCMV) infections can cause endotheliitis which is associated with an elevation in the intraocular pressure (IOP). However, the mechanism of the IOP elevation has not been established. The purpose of this study was to determine whether HCMV strains which are capable of infecting corneal endothelial cells can also replicate and induce anti-viral responses, and can reorganize the actin cytoskeleton in trabecular meshwork cells. STUDY

designExperimental study design.

methodsCultured primary human trabecular meshwork cells (HTMCs) were infected with the Towne or TB40/E strains of HCMV. TB40/E is trophic for vascular endothelial and corneal endothelial cells. Real-time PCR, western blot, and fluorescent immunostaining have been used to determine whether HCMV-infected HTMCs will support the expression of viral mRNA and protein, allow viral replication, and elicit anti-viral host responses. We also determined whether lytic replication was present after HCMV infection.

resultsHCMV infection led to the expression of viral mRNA and proteins of IE1, glycoprotein B(gB), and pp65. TB40/E infection induced interferon-β, a sign of host anti-viral immune response and monocyte chemotactic protein-1 (MCP-1) as IOP-related chemokine. Together with the induction of the regulators of actin cytoskeleton, myosin phosphatase Rho interacting protein (MPRIP) and MCP-1, TB40/E induced a high level of expression of viral proteins, including IE1, gB, and pp65 as well as actin stress fiber formation, and achieved pathogenically high viral titers.

conclusionsHuman trabecular meshwork cells support the replication of endotheliotropic TB40/E strain of HCMV which indicates that this strain may have high virulence for trabecular meshwork.

Indexed as

Blotting, WesternCell LineCytomegalovirusCytomegalovirus InfectionsDNA, ViralEndothelial CellsEye Infections, ViralHumansImmunohistochemistryMicroscopy, Electron, TransmissionReal-Time Polymerase Chain ReactionTrabecular MeshworkVirus ReplicationDNA, ViralCorneal endothelial cellsCytomegalovirusEndotheliitisSecondary glaucomaTrabecular meshwork

Identifiers

PMID30191418
OpenAlexW2890644122

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.