Serveur d'exploration sur le lymphœdème

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In Vivo Molecular Optical Coherence Tomography of Lymphatic Vessel Endothelial Hyaluronan Receptors

Identifieur interne : 000872 ( Main/Exploration ); précédent : 000871; suivant : 000873

In Vivo Molecular Optical Coherence Tomography of Lymphatic Vessel Endothelial Hyaluronan Receptors

Auteurs : Peng Si [États-Unis] ; Debasish Sen [États-Unis] ; Rebecca Dutta [États-Unis] ; Siavash Yousefi [États-Unis] ; Roopa Dalal [États-Unis] ; Yonatan Winetraub [États-Unis] ; Orly Liba [États-Unis] ; Adam De La Zerda [États-Unis]

Source :

RBID : PMC:5430649

Abstract

Optical Coherence Tomography (OCT) imaging of living subjects offers increased depth of penetration while maintaining high spatial resolution when compared to other optical microscopy techniques. However, since most protein biomarkers do not exhibit inherent contrast detectable by OCT, exogenous contrast agents must be employed for imaging specific cellular biomarkers of interest. While a number of OCT contrast agents have been previously studied, demonstrations of molecular targeting with such agents in live animals have been historically challenging and notably limited in success. Here we demonstrate for the first time that microbeads (µBs) can be used as contrast agents to target cellular biomarkers in lymphatic vessels and can be detected by OCT using a phase variance algorithm. This molecular OCT method enables in vivo imaging of the expression profiles of lymphatic vessel endothelial hyaluronan receptor 1 (LYVE-1), a biomarker that plays crucial roles in inflammation and tumor metastasis. In vivo OCT imaging of LVYE-1 showed that the biomarker was significantly down-regulated during inflammation induced by acute contact hypersensitivity (CHS). Our work demonstrated a powerful molecular imaging tool that can be used for high resolution studies of lymphatic function and dynamics in models of inflammation, tumor development, and other lymphatic diseases.


Url:
DOI: 10.1038/s41598-017-01172-x
PubMed: 28439123
PubMed Central: 5430649


Affiliations:


Links toward previous steps (curation, corpus...)


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Molecular Optical Coherence Tomography of Lymphatic Vessel Endothelial Hyaluronan Receptors</title>
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<institution>Bio-X Program, Stanford University,</institution>
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Stanford, California 94305 USA</nlm:aff>
<country xml:lang="fr">États-Unis</country>
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<region type="state">Californie</region>
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<wicri:cityArea>Stanford</wicri:cityArea>
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<author>
<name sortKey="De La Zerda, Adam" sort="De La Zerda, Adam" uniqKey="De La Zerda A" first="Adam" last="De La Zerda">Adam De La Zerda</name>
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<nlm:aff id="Aff1">Molecular Imaging Program at Stanford, Stanford, California 94305 USA</nlm:aff>
<country xml:lang="fr">États-Unis</country>
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<region type="state">Californie</region>
</placeName>
<wicri:cityArea>Molecular Imaging Program at Stanford, Stanford</wicri:cityArea>
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<institution>Department of Structural Biology,</institution>
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299 Campus Drive West, Stanford, California 94305 USA</nlm:aff>
<country xml:lang="fr">États-Unis</country>
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<region type="state">Californie</region>
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<wicri:cityArea>299 Campus Drive West, Stanford</wicri:cityArea>
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<institution>Department of Electrical Engineering,</institution>
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350 Serra Mall, Stanford, California 94305 USA</nlm:aff>
<country xml:lang="fr">États-Unis</country>
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<region type="state">Californie</region>
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<institution>Bio-X Program, Stanford University,</institution>
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Stanford, California 94305 USA</nlm:aff>
<country xml:lang="fr">États-Unis</country>
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<region type="state">Californie</region>
</placeName>
<wicri:cityArea>Stanford</wicri:cityArea>
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<series>
<title level="j">Scientific Reports</title>
<idno type="eISSN">2045-2322</idno>
<imprint>
<date when="2017">2017</date>
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<div type="abstract" xml:lang="en">
<p>Optical Coherence Tomography (OCT) imaging of living subjects offers increased depth of penetration while maintaining high spatial resolution when compared to other optical microscopy techniques. However, since most protein biomarkers do not exhibit inherent contrast detectable by OCT, exogenous contrast agents must be employed for imaging specific cellular biomarkers of interest. While a number of OCT contrast agents have been previously studied, demonstrations of molecular targeting with such agents in live animals have been historically challenging and notably limited in success. Here we demonstrate for the first time that microbeads (µBs) can be used as contrast agents to target cellular biomarkers in lymphatic vessels and can be detected by OCT using a phase variance algorithm. This molecular OCT method enables
<italic>in vivo</italic>
imaging of the expression profiles of lymphatic vessel endothelial hyaluronan receptor 1 (LYVE-1), a biomarker that plays crucial roles in inflammation and tumor metastasis.
<italic>In vivo</italic>
OCT imaging of LVYE-1 showed that the biomarker was significantly down-regulated during inflammation induced by acute contact hypersensitivity (CHS). Our work demonstrated a powerful molecular imaging tool that can be used for high resolution studies of lymphatic function and dynamics in models of inflammation, tumor development, and other lymphatic diseases.</p>
</div>
</front>
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<name sortKey="Yousefi, Siavash" sort="Yousefi, Siavash" uniqKey="Yousefi S" first="Siavash" last="Yousefi">Siavash Yousefi</name>
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</record>

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