Evidence map›Paper›PMID 25708987›Full record

ArticleExperimental neurology2015

Focal transient CNS vessel leak provides a tissue niche for sequential immune cell accumulation during the asymptomatic phase of EAE induction.

Deborah S Barkauskas, R Dixon Dorand, Jay T Myers, Teresa A Evans, Kestutis J Barkauskas, David Askew, Robert Purgert, Alex Y Huang

Open access · hybridAbstract read
In one paragraph

Article in Experimental neurology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

27 citing papers in PubMed, 53 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Embryonic Pericytes Promote Microglial Homeostasis and Their Effects on Neural Progenitors in the Developing Cerebral Cortex.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  11. The behavior and functions of embryonic microglia.Anatomical science international · 2022
    Review
  12. Article
  13. Review
  14. Review
  15. Review
  16. Review
  17. Histamine Induces Microglia Activation and the Release of Proinflammatory Mediators in Rat Brain Via HJournal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2020
    Article
  18. Review
  19. Review
  20. To the Brain and Back: Migratory Paths of Dendritic Cells in Multiple Sclerosis.Journal of neuropathology and experimental neurology · 2018
    Review
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

8 authors at 2 institutions in 1 country.

Deborah S BarkauskasDivision of Pediatric Hematology-Oncology, Department of Pediatrics, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA.
R Dixon DorandDepartment of Pathology, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA.
Jay T MyersDivision of Pediatric Hematology-Oncology, Department of Pediatrics, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA.
Teresa A EvansDepartment of Neurosciences, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA.
Kestutis J BarkauskasDepartment of Biomedical Engineering, Case Western Reserve University School of Engineering, Cleveland, OH 44106, USA.
David AskewDivision of Pediatric Hematology-Oncology, Department of Pediatrics, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA.
Robert PurgertDivision of Pediatric Hematology-Oncology, Department of Pediatrics, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA.
Alex Y HuangDivision of Pediatric Hematology-Oncology, Department of Pediatrics, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA; Department of Pathology, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA. Electronic address: alex.y.huang@case.edu.
University School · USCase Western Reserve University · US

Funding

Clinical and Translational Science Collaborative of ClevelandUL1TR000439 · NCATS · CASE WESTERN RESERVE UNIVERSITY · PI KONSTAN, MICHAEL W. · 2012 to 2016
$50.0M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM007250 · NIGMS · CASE WESTERN RESERVE UNIVERSITY · PI HUANG, ALEX YEE-CHEN · 1985 to 2023
$33.4M
Interdisciplinary Biomedical Imaging Training ProgramT32EB007509 · NIBIB · CASE WESTERN RESERVE UNIVERSITY · PI DAVID Lynn WILSON, Xin Yu · 2007 to 2026
$5.6M
Clinical and Translational Science Collaborative of ClevelandTL1TR000441 · NCATS · CASE WESTERN RESERVE UNIVERSITY · PI KONSTAN, MICHAEL W. · 2012 to 2016
$2.8M
Novel Fast Imaging and Reconstruction Strategies for Dynamic MRIR00EB011527 · NIBIB · CASE WESTERN RESERVE UNIVERSITY · PI SEIBERLICH, NICOLE · 2012 to 2014
$719k
NCATS NIH HHS TL1 TR000441NCATS NIH HHS UL1 TR000439NIBIB NIH HHS EB007509NIBIB NIH HHS R00 EB011527NIBIB NIH HHS R00EB011527NIBIB NIH HHS T32 EB007509NIGMS NIH HHS GM007250NIGMS NIH HHS T32 GM007250
6 · The paper itself

Abstract

Peripheral immune cells are critical to the pathogenesis of neurodegenerative diseases including multiple sclerosis (MS) (Hendriks et al., 2005; Kasper and Shoemaker, 2010). However, the precise sequence of tissue events during the early asymptomatic induction phase of experimental autoimmune encephalomyelitis (EAE) pathogenesis remains poorly defined. Due to the spatial-temporal constrains of traditional methods used to study this disease, most studies had been performed in the spine during peak clinical disease; thus the debate continues as to whether tissue changes such as vessel disruption represent a cause or a byproduct of EAE pathophysiology in the cortex. Here, we provide dynamic, high-resolution information on the evolving structural and cellular processes within the gray matter of the mouse cortex during the first 12 asymptomatic days of EAE induction. We observed that transient focal vessel disruptions precede microglia activation, followed by infiltration of and directed interaction between circulating dendritic cells and T cells. Histamine antagonist minimizes but not completely ameliorates blood vessel leaks. Histamine H1 receptor blockade prevents early microglia function, resulting in subsequent reduction in immune cell accumulation, disease incidence and clinical severity.

Indexed as

AnimalsAntigen-Presenting CellsBlood-Brain BarrierCerebral CortexEncephalomyelitis, Autoimmune, ExperimentalGray MatterHistamine H1 AntagonistsHydroxyzineMacrophage ActivationMiceMice, TransgenicPertussis ToxinSubarachnoid SpaceT-LymphocytesHistamine H1 AntagonistsHydroxyzinePertussis Toxin

Identifiers

PMID25708987
PMCPMC4382434
OpenAlexW2028417725

What OpenQuestion holds

Textmetadata
LicenceTDM
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.