Show simple item record

dc.contributor.authorRawson, FJ
dc.contributor.authorHicks, J
dc.contributor.authorDodd, N
dc.contributor.authorAbate, W
dc.contributor.authorGarrett, DJ
dc.contributor.authorYip, N
dc.contributor.authorFejer, Gyorgy
dc.contributor.authorDownard, AJ
dc.contributor.authorBaronian, KHR
dc.contributor.authorJackson, SK
dc.contributor.authorMendes, PM
dc.date.accessioned2017-03-10T15:47:53Z
dc.date.available2017-03-10T15:47:53Z
dc.date.issued2015-10-28
dc.identifier.issn1944-8244
dc.identifier.issn1944-8252
dc.identifier.urihttp://hdl.handle.net/10026.1/8607
dc.description.abstract

Herein, we report a highly sensitive electrocatalytic sensor-cell construct that can electrochemically communicate with the internal environment of immune cells (e.g., macrophages) via the selective monitoring of a particular reactive oxygen species (ROS), hydrogen peroxide. The sensor, which is based on vertically aligned single-walled carbon nanotubes functionalized with an osmium electrocatalyst, enabled the unprecedented detection of a local intracellular "pulse" of ROS on a short second time scale in response to bacterial endotoxin (lipopolysaccharide-LPS) stimulation. Our studies have shown that this initial pulse of ROS is dependent on NADPH oxidase (NOX) and toll like receptor 4 (TLR4). The results suggest that bacteria can induce a rapid intracellular pulse of ROS in macrophages that initiates the classical innate immune response of these cells to infection.

dc.format.extent23527-23537
dc.format.mediumPrint-Electronic
dc.languageen
dc.language.isoeng
dc.publisherAmerican Chemical Society (ACS)
dc.subjectintracellular sensor
dc.subjectelectrocatalytic sensor
dc.subjectcarbon nanotubes
dc.subjectreactive oxygen species
dc.subjecthydrogen peroxide
dc.subjectmacrophage cells
dc.titleFast, Ultrasensitive Detection of Reactive Oxygen Species Using a Carbon Nanotube Based-Electrocatalytic Intracellular Sensor
dc.typejournal-article
dc.typeJournal Article
dc.typeResearch Support, Non-U.S. Gov't
plymouth.author-urlhttps://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000363994700022&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=11bb513d99f797142bcfeffcc58ea008
plymouth.issue42
plymouth.volume7
plymouth.publication-statusPublished
plymouth.journalACS Applied Materials & Interfaces
dc.identifier.doi10.1021/acsami.5b06493
plymouth.organisational-group/Plymouth
plymouth.organisational-group/Plymouth/Faculty of Health
plymouth.organisational-group/Plymouth/Faculty of Health/School of Biomedical Sciences
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA/UoA01 Clinical Medicine
plymouth.organisational-group/Plymouth/Research Groups
plymouth.organisational-group/Plymouth/Research Groups/Institute of Translational and Stratified Medicine (ITSMED)
plymouth.organisational-group/Plymouth/Research Groups/Institute of Translational and Stratified Medicine (ITSMED)/CBR
plymouth.organisational-group/Plymouth/Users by role
plymouth.organisational-group/Plymouth/Users by role/Academics
plymouth.organisational-group/Plymouth/Users by role/Researchers in ResearchFish submission
dc.publisher.placeUnited States
dc.identifier.eissn1944-8252
dc.rights.embargoperiodNot known
rioxxterms.versionofrecord10.1021/acsami.5b06493
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserved
rioxxterms.typeJournal Article/Review
plymouth.funderEstablishment of non-transformed, continuously growing, alternatively activated mouse macrophage cell lines::NC3Rs


Files in this item

Thumbnail
Thumbnail

This item appears in the following Collection(s)

Show simple item record


All items in PEARL are protected by copyright law.
Author manuscripts deposited to comply with open access mandates are made available in accordance with publisher policies. Please cite only the published version using the details provided on the item record or document. In the absence of an open licence (e.g. Creative Commons), permissions for further reuse of content should be sought from the publisher or author.
Theme by 
Atmire NV