Evidence map›Paper›PMID 37776464›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2024

Evaluation of Tight Junction Integrity in Brain Endothelial Cells Using Confocal Microscopy.

Himakarnika Alluri, Chander Sekhar Peddaboina, Binu Tharakan

Open access · greenAbstract read
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
10.7field-weighted citation impact, top 1% 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

9 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. 3DFrontiers in pharmacology · 2025
    Review
  7. Article
  8. Review
  9. 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

3 authors at 3 institutions in 1 country.

Himakarnika AlluriPrecision for Medicine, Redwood City, CA, USA.
Chander Sekhar PeddaboinaOxford Biotherapeutics Inc., San Jose, CA, USA.
Binu TharakanDepartment of Surgery, Morehouse School of Medicine, Atlanta, GA, USA. btharakan@msm.edu.
Atara Biotherapeutics (United States) · USMorehouse School of Medicine · USPrecision for Medicine (United States) · US

Funding

Influence of Age and Sex on Cerebral Edema Formation Following Traumatic Brain InjurySC3NS127765 · NINDS · MOREHOUSE SCHOOL OF MEDICINE · PI THARAKAN, BINU · 2022 to 2025
$423k
NINDS NIH HHS SC3 NS127765
6 · The paper itself

Abstract

The blood-brain barrier (BBB) is a highly complex and dynamic microvascular barrier that protects the brain parenchyma from the entry of pathogens, toxins, and other macromolecules and is a critical structure that helps to maintain brain homeostasis. The BBB is formed mainly by brain capillary endothelial cells and perivascular astrocytes and pericytes. One of the primary properties of the BBB is a tight regulation of paracellular permeability due to the presence of tight junctional complexes (also, adherens and gap junctions) between the neighboring microvascular endothelial cells. Alterations in the assembly of the tight junctions impair BBB properties, particularly influenced barrier integrity and permeability. The tight junctions of the BBB are mainly composed of proteins including claudins, occludin, and zonula occludens-1 (ZO-1). Zonula occludens-1 binds to the actin cytoskeleton, and its localization provides valuable information on the status of BBB integrity and permeability. Immunofluorescence localization of ZO-1 and/or other tight junction proteins is a reliable indicator of barrier integrity and permeability in microvascular endothelial cells. In microvascular endothelial cells, f-actin stress fiber formation significantly influences the rate and size of the inter-endothelial cell gap that form as cells retract from their borders. Rhodamine phalloidin is a popular conjugate used as a fluorescent label for f-actin. Herein, we describe the procedures for ZO-1 immunofluorescence and f-actin labeling followed by confocal microscopic imaging to determine barrier integrity and tight junction organization in brain microvascular endothelial cells in vitro.

Indexed as

Endothelial CellsTight JunctionsActinsBlood-Brain BarrierBrainMicroscopy, ConfocalActinsBlood-brain barrierf-actinTight junction proteinsZonula occludens-1 immunofluorescence

Identifiers

PMID37776464
PMCPMC12034389
OpenAlexW4387199909

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.