Evidence map›Paper›PMID 37504986›Full record

ArticleMembranes2023

Hypo-Osmotic Stress and Pore-Forming Toxins Adjust the Lipid Order in Sheep Red Blood Cell Membranes.

Rose Whiting, Sevio Stanton, Maryna Kucheriava, Aviana R Smith, Matt Pitts, Daniel Robertson, Jacob Kammer, Zhiyu Li, Daniel Fologea

Open access · goldAbstract read
In one paragraph

Article in Membranes, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 37% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

9 authors at 1 institution in 1 country.

Rose WhitingDepartment of Physics, Boise State University, Boise, ID 83725, USA.
Sevio StantonDepartment of Physics, Boise State University, Boise, ID 83725, USA.ORCID 0000-0003-1078-9132
Maryna KucheriavaDepartment of Physics, Boise State University, Boise, ID 83725, USA.
Aviana R SmithDepartment of Physics, Boise State University, Boise, ID 83725, USA.ORCID 0009-0005-1505-6212
Matt PittsDepartment of Physics, Boise State University, Boise, ID 83725, USA.
Daniel RobertsonDepartment of Physics, Boise State University, Boise, ID 83725, USA.
Jacob KammerDepartment of Physics, Boise State University, Boise, ID 83725, USA.
Zhiyu LiDepartment of Physics, Boise State University, Boise, ID 83725, USA.
Daniel FologeaDepartment of Physics, Boise State University, Boise, ID 83725, USA.
Boise State University · US

Funding

Women's health: interplay of maternal diet and key demographics on neurological health in the rural frontier and remote WestP20GM103408 · NIGMS · UNIVERSITY OF IDAHO · PI Carolyn Hovde Bohach · 2012 to 2026
$59.8M
VPS35 D620N inhibits autophagy through disrupted hyaluronic acid-CD44 signalingP20GM109095 · NIGMS · BOISE STATE UNIVERSITY · PI OXFORD, JULIA THOM · 2014 to 2023
$22.7M
The role of the innate immune response in adenovirus Ad14p1 immunopathogenesisP20GM109007 · NIGMS · IDAHO VETERANS RESEARCH / EDUCATION FDN · PI STEVENS, DENNIS L · 2016 to 2021
$10.0M
NIGMS NIH HHS P20 GM103408NIGMS NIH HHS P20 GM109007NIGMS NIH HHS P20GM109007NIGMS NIH HHS P20 GM109095NIH HHS P20GM103408NIH HHS P20GM109095
6 · The paper itself

Abstract

Lipid ordering in cell membranes has been increasingly recognized as an important factor in establishing and regulating a large variety of biological functions. Multiple investigations into lipid organization focused on assessing ordering from temperature-induced phase transitions, which are often well outside the physiological range. However, particular stresses elicited by environmental factors, such as hypo-osmotic stress or protein insertion into membranes, with respect to changes in lipid status and ordering at constant temperature are insufficiently described. To fill these gaps in our knowledge, we exploited the well-established ability of environmentally sensitive membrane probes to detect intramembrane changes at the molecular level. Our steady state fluorescence spectroscopy experiments focused on assessing changes in optical responses of Laurdan and diphenylhexatriene upon exposure of red blood cells to hypo-osmotic stress and pore-forming toxins at room temperature. We verified our utilized experimental systems by a direct comparison of the results with prior reports on artificial membranes and cholesterol-depleted membranes undergoing temperature changes. The significant changes observed in the lipid order after exposure to hypo-osmotic stress or pore-forming toxins resembled phase transitions of lipids in membranes, which we explained by considering the short-range interactions between membrane components and the hydrophobic mismatch between membrane thickness and inserted proteins. Our results suggest that measurements of optical responses from the membrane probes constitute an appropriate method for assessing the status of lipids and phase transitions in target membranes exposed to mechanical stresses or upon the insertion of transmembrane proteins.

Indexed as

diphenylhexatrienehypo-osmotic shockLaurdanlipid orderphase transitionpore-forming toxins

Identifiers

PMID37504986
PMCPMC10385129
OpenAlexW4382135065

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.