Evidence map›Paper›PMID 29327203›Full record

ArticleMolecular neurobiology2018

Loss of Cx43-Mediated Functional Gap Junction Communication in Meningeal Fibroblasts Following Mouse Hepatitis Virus Infection.

Abhishek Bose, Rahul Basu, Mahua Maulik, Jayasri Das Sarma

Open access · greenAbstract read
In one paragraph

Article in Molecular neurobiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.7field-weighted citation impact, top 30% 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, 24 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

4 authors at 1 institution in 1 country.

Abhishek BoseDepartment of Biological Sciences, Indian Institute of Science Education and Research Kolkata (IISER-K), Mohanpur, Nadia, West Bengal, 741246, India.
Rahul BasuDepartment of Biological Sciences, Indian Institute of Science Education and Research Kolkata (IISER-K), Mohanpur, Nadia, West Bengal, 741246, India.
Mahua MaulikDepartment of Biological Sciences, Indian Institute of Science Education and Research Kolkata (IISER-K), Mohanpur, Nadia, West Bengal, 741246, India.
Jayasri Das SarmaDepartment of Biological Sciences, Indian Institute of Science Education and Research Kolkata (IISER-K), Mohanpur, Nadia, West Bengal, 741246, India. dassarmaj@iiserkol.ac.in.ORCID http://orcid.org/0000-0002-3980-4060
Indian Institute of Science Education and Research Kolkata · IN

Funding

Department of Biotechnology , Ministry of Science and Technology BT/PR14260/MED/30/437/2010Department of Biotechnology , Ministry of Science and Technology BT/PR4530/MED/30/715/2012National Multiple Sclerosis Society RG3774A2/1
6 · The paper itself

Abstract

Mouse hepatitis virus (MHV) infection causes meningoencephalitis by disrupting the neuro-glial and glial-pial homeostasis. Recent studies suggest that MHV infection alters gap junction protein connexin 43 (Cx43)-mediated intercellular communication in brain and primary cultured astrocytes. In addition to astrocytes, meningeal fibroblasts also express high levels of Cx43. Fibroblasts in the meninges together with the basal lamina and the astrocyte endfeet forms the glial limitans superficialis as part of the blood-brain barrier (BBB). Alteration of glial-pial gap junction intercellular communication (GJIC) in MHV infection has the potential to affect the integrity of BBB. Till date, it is not known if viral infection can modulate Cx43 expression and function in cells of the brain meninges and thus affect BBB permeability. In the present study, we have investigated the effect of MHV infection on Cx43 localization and function in mouse brain meningeal cells and primary meningeal fibroblasts. Our results show that MHV infection reduces total Cx43 levels and causes its intracellular retention in the perinuclear compartments reducing its surface expression. Reduced trafficking of Cx43 to the cell surface in MHV-infected cells is associated with loss functional GJIC. Together, these data suggest that MHV infection can directly affect expression and cellular distribution of Cx43 resulting in loss of Cx43-mediated GJIC in meningeal fibroblasts, which may be associated with altered BBB function observed in acute infection.

Indexed as

AnimalsCells, CulturedConnexin 43Endoplasmic ReticulumFibroblastsGap JunctionsHepatitis, Viral, AnimalInflammationMeningesMice, Inbred C57BLMurine hepatitis virusProtein AggregatesVimentinConnexin 43Protein AggregatesVimentinBlood–brain barrier (BBB)Connexin 43Gap junction intercellular communicationIntracranial infectionMouse hepatitis virus (MHV)Primary meningeal fibroblast culture

Identifiers

PMID29327203
PMCPMC7090783
OpenAlexW2784271602

What Socratic 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 Socratic graph.