Intact mammalian cell function on semiconductor nanowire arrays: new perspectives for cell-based biosensing.
Identifieur interne : 001319 ( Main/Exploration ); précédent : 001318; suivant : 001320Intact mammalian cell function on semiconductor nanowire arrays: new perspectives for cell-based biosensing.
Auteurs : RBID : pubmed:21290597English descriptors
- KwdEn :
- MESH :
- chemical , chemistry : Arsenicals, Indium.
- chemistry : Nanowires.
- metabolism : Ganglia, Spinal, Neurons.
- Animals, Biosensing Techniques, Humans, Microscopy, Confocal, Rats, Semiconductors, Structure-Activity Relationship.
Abstract
Nanowires (NWs) are attracting more and more interest due to their potential cellular applications, such as delivery of compounds or sensing platforms. Arrays of vertical indium-arsenide (InAs) NWs are interfaced with human embryonic kidney cells and rat embryonic dorsal root ganglion neurons. A selection of critical cell functions and pathways are shown not to be impaired, including cell adhesion, membrane integrity, intracellular enzyme activity, DNA uptake, cytosolic and membrane protein expression, and the neuronal maturation pathway. The results demonstrate the low invasiveness of InAs NW arrays, which, combined with the unique physical properties of InAs, open up their potential for cellular investigations.
DOI: 10.1002/smll.201001642
PubMed: 21290597
Links toward previous steps (curation, corpus...)
Le document en format XML
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<author><name sortKey="Berthing, Trine" uniqKey="Berthing T">Trine Berthing</name>
<affiliation wicri:level="1"><nlm:affiliation>Bionanotechnology and Nanomedicine Laboratory, Department of Neuroscience and Pharmacology & Nano-science Center, University of Copenhagen, Universitetsparken 5, DK-2100, Copenhagen, Denmark.</nlm:affiliation>
<country xml:lang="fr">Danemark</country>
<wicri:regionArea>Bionanotechnology and Nanomedicine Laboratory, Department of Neuroscience and Pharmacology & Nano-science Center, University of Copenhagen, Universitetsparken 5, DK-2100, Copenhagen</wicri:regionArea>
</affiliation>
</author>
<author><name sortKey="Bonde, Sara" uniqKey="Bonde S">Sara Bonde</name>
</author>
<author><name sortKey="S Rensen, Claus B" uniqKey="S Rensen C">Claus B Sørensen</name>
</author>
<author><name sortKey="Utko, Pawel" uniqKey="Utko P">Pawel Utko</name>
</author>
<author><name sortKey="Nyg Rd, Jesper" uniqKey="Nyg Rd J">Jesper Nygård</name>
</author>
<author><name sortKey="Martinez, Karen L" uniqKey="Martinez K">Karen L Martinez</name>
</author>
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<publicationStmt><date when="2011">2011</date>
<idno type="doi">10.1002/smll.201001642</idno>
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<term>Arsenicals (chemistry)</term>
<term>Biosensing Techniques</term>
<term>Ganglia, Spinal (metabolism)</term>
<term>Humans</term>
<term>Indium (chemistry)</term>
<term>Microscopy, Confocal</term>
<term>Nanowires (chemistry)</term>
<term>Neurons (metabolism)</term>
<term>Rats</term>
<term>Semiconductors</term>
<term>Structure-Activity Relationship</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en"><term>Arsenicals</term>
<term>Indium</term>
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<keywords scheme="MESH" qualifier="chemistry" xml:lang="en"><term>Nanowires</term>
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<keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Ganglia, Spinal</term>
<term>Neurons</term>
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<keywords scheme="MESH" xml:lang="en"><term>Animals</term>
<term>Biosensing Techniques</term>
<term>Humans</term>
<term>Microscopy, Confocal</term>
<term>Rats</term>
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<front><div type="abstract" xml:lang="en">Nanowires (NWs) are attracting more and more interest due to their potential cellular applications, such as delivery of compounds or sensing platforms. Arrays of vertical indium-arsenide (InAs) NWs are interfaced with human embryonic kidney cells and rat embryonic dorsal root ganglion neurons. A selection of critical cell functions and pathways are shown not to be impaired, including cell adhesion, membrane integrity, intracellular enzyme activity, DNA uptake, cytosolic and membrane protein expression, and the neuronal maturation pathway. The results demonstrate the low invasiveness of InAs NW arrays, which, combined with the unique physical properties of InAs, open up their potential for cellular investigations.</div>
</front>
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<JournalIssue CitedMedium="Internet"><Volume>7</Volume>
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<Title>Small (Weinheim an der Bergstrasse, Germany)</Title>
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<ArticleTitle>Intact mammalian cell function on semiconductor nanowire arrays: new perspectives for cell-based biosensing.</ArticleTitle>
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<Abstract><AbstractText>Nanowires (NWs) are attracting more and more interest due to their potential cellular applications, such as delivery of compounds or sensing platforms. Arrays of vertical indium-arsenide (InAs) NWs are interfaced with human embryonic kidney cells and rat embryonic dorsal root ganglion neurons. A selection of critical cell functions and pathways are shown not to be impaired, including cell adhesion, membrane integrity, intracellular enzyme activity, DNA uptake, cytosolic and membrane protein expression, and the neuronal maturation pathway. The results demonstrate the low invasiveness of InAs NW arrays, which, combined with the unique physical properties of InAs, open up their potential for cellular investigations.</AbstractText>
<CopyrightInformation>Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Berthing</LastName>
<ForeName>Trine</ForeName>
<Initials>T</Initials>
<Affiliation>Bionanotechnology and Nanomedicine Laboratory, Department of Neuroscience and Pharmacology & Nano-science Center, University of Copenhagen, Universitetsparken 5, DK-2100, Copenhagen, Denmark.</Affiliation>
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<Author ValidYN="Y"><LastName>Sørensen</LastName>
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<Chemical><RegistryNumber>1303-11-3</RegistryNumber>
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<QualifierName MajorTopicYN="N">metabolism</QualifierName>
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<MeshHeading><DescriptorName MajorTopicYN="N">Rats</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="Y">Semiconductors</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N">Structure-Activity Relationship</DescriptorName>
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