Evidence map›Paper›PMID 24992043›Full record

ArticleExperimental cell research2014

The formation of cortical actin arrays in human trabecular meshwork cells in response to cytoskeletal disruption.

Kaitlin C Murphy, Joshua T Morgan, Joshua A Wood, Adeline Sadeli, Christopher J Murphy, Paul Russell

Abstract read
In one paragraph

Article in Experimental cell research, 2014. 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
1.4field-weighted citation impact, top 19% 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, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Ripasudil in a Model of Pigmentary Glaucoma.Translational vision science & technology · 2020
    Article
  4. Impact of pigment dispersion on trabecular meshwork cells.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2019
    Article
  5. Article
  6. Cross-linked actin networks (CLANs) in glaucoma.Experimental eye research · 2017
    Review
  7. Article
  8. Article
  9. 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 1 institution in 1 country.

Kaitlin C Murphy *Department of Biomedical Engineering / University of California, Davis.
Joshua T Morgan *Department of Surgical and Radiological Sciences, School of Veterinary Medicine / University of California, Davis.
Joshua A WoodDepartment of Surgical and Radiological Sciences, School of Veterinary Medicine / University of California, Davis.
Adeline SadeliDepartment of Surgical and Radiological Sciences, School of Veterinary Medicine / University of California, Davis.
Christopher J MurphyDepartment of Surgical and Radiological Sciences, School of Veterinary Medicine / University of California, Davis.
Paul RussellDepartment of Surgical and Radiological Sciences, School of Veterinary Medicine / University of California, Davis.
University of California, Davis · US

Funding

VISION RESEARCH CORE GRANTP30EY012576 · NEI · UNIVERSITY OF CALIFORNIA DAVIS · PI LISA M OAKES · 1999 to 2026
$18.9M
Biophysical Cues and Corneal Wound HealingR01EY019970 · NEI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI MURPHY, CHRISTOPHER JOHN · 2011 to 2020
$3.5M
Role of Biophysical Cues in the Pathogenesis of GlaucomaR01EY019475 · NEI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI RUSSELL, PAUL · 2010 to 2013
$1.5M
NEI NIH HHS P30 EY012576NEI NIH HHS P30EY12576NEI NIH HHS R01 EY019475NEI NIH HHS R01EY019475NEI NIH HHS R01 EY019970NEI NIH HHS R01EY019970
6 · The paper itself

Abstract

The cytoskeleton of human trabecular meshwork (HTM) cells is known to be altered in glaucoma and has been hypothesized to reduce outflow facility through contracting the HTM tissue. Latrunculin B (Lat-B) and Rho-associated protein kinase (ROCK) inhibitors disrupt the actin cytoskeleton and are in clinical trials as glaucoma therapeutics. We have previously reported a transient increase in HTM cell stiffness peaking at 90 min after Lat-B treatment with a return to pretreatment values after 270 min. We hypothesize that changes in actin morphology correlate with alterations in cell stiffness induced by Lat-B but this is not a general consequence of other cytoskeletal disrupting agents such as Rho kinase inhibitors. We treated HTM cells with 2 µM Lat-B or 100 µM Y-27632 and allowed the cells to recover for 30-270 min. While examining actin morphology in Lat-B treated cells, we observed striking cortical actin arrays (CAAs). The percentage of CAA positive cells (CPCs) was time dependent and exceeded 30% at 90 min and decreased after 270 min. Y-27632 treated cells exhibited few CAAs and no changes in cell stiffness. Together, these data suggest that the increase in cell stiffness after Lat-B treatment is correlated with CAAs.

Indexed as

ActinsAmidesAntihypertensive AgentsBridged Bicyclo Compounds, HeterocyclicCell Physiological PhenomenaCells, CulturedCytoskeletonHumansImage Processing, Computer-AssistedPyridinesrho-Associated KinasesThiazolidinesTrabecular MeshworkActinsAmidesAntihypertensive AgentsBridged Bicyclo Compounds, Heterocycliclatrunculin BPyridinesrho-Associated KinasesThiazolidinesY 27632ActinCytoskeletonLatrunculin BRho-associated protein kinaseTrabecular Meshwork

Identifiers

PMID24992043
PMCPMC4178168
OpenAlexW2000356468

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.