Science to Practice: Highly shifted proton MR imaging--a shift toward better cell tracking?
Identifieur interne : 000149 ( PubMed/Corpus ); précédent : 000148; suivant : 000150Science to Practice: Highly shifted proton MR imaging--a shift toward better cell tracking?
Auteurs : Jeff W M. BulteSource :
- Radiology [ 1527-1315 ] ; 2014.
English descriptors
- KwdEn :
- MESH :
- chemical : Quaternary Ammonium Compounds.
- methods : Cell Tracking, Image Enhancement, Magnetic Resonance Imaging.
- pathology : Fibrosarcoma, Granuloma, Macrophages.
- Animals, Female, Humans.
Abstract
Summary A "hot spot" magnetic resonance (MR) imaging cell tracking technique has been developed that allows direct detection of dysprosium- or thulium-1,4,7,10-tetraazacyclododecane-α,α',α'',α'''-tetramethyl-1,4,7,10-tetraacetic acid (DOTMA)-labeled protons inside cells. These highly shifted protons may allow specific detection of multiple cell types because it does not rely on acquiring the proton signal from bulk water.
DOI: 10.1148/radiol.14141410
PubMed: 25153271
Links to Exploration step
pubmed:25153271Le document en format XML
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<author><name sortKey="Bulte, Jeff W M" sort="Bulte, Jeff W M" uniqKey="Bulte J" first="Jeff W M" last="Bulte">Jeff W M. Bulte</name>
<affiliation><nlm:affiliation>Russell H. Morgan Department of Radiology and Radiological Science and Engineering, Division of MR Research, Cellular Imaging Section, Institute for Cell Engineering The Johns Hopkins University School of Medicine 720 Rutland Ave, 217 Traylor Baltimore, MD 21205.</nlm:affiliation>
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<author><name sortKey="Bulte, Jeff W M" sort="Bulte, Jeff W M" uniqKey="Bulte J" first="Jeff W M" last="Bulte">Jeff W M. Bulte</name>
<affiliation><nlm:affiliation>Russell H. Morgan Department of Radiology and Radiological Science and Engineering, Division of MR Research, Cellular Imaging Section, Institute for Cell Engineering The Johns Hopkins University School of Medicine 720 Rutland Ave, 217 Traylor Baltimore, MD 21205.</nlm:affiliation>
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<series><title level="j">Radiology</title>
<idno type="eISSN">1527-1315</idno>
<imprint><date when="2014" type="published">2014</date>
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<term>Cell Tracking (methods)</term>
<term>Female</term>
<term>Fibrosarcoma (pathology)</term>
<term>Granuloma (pathology)</term>
<term>Humans</term>
<term>Image Enhancement (methods)</term>
<term>Macrophages (pathology)</term>
<term>Magnetic Resonance Imaging (methods)</term>
<term>Quaternary Ammonium Compounds</term>
</keywords>
<keywords scheme="MESH" type="chemical" xml:lang="en"><term>Quaternary Ammonium Compounds</term>
</keywords>
<keywords scheme="MESH" qualifier="methods" xml:lang="en"><term>Cell Tracking</term>
<term>Image Enhancement</term>
<term>Magnetic Resonance Imaging</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Fibrosarcoma</term>
<term>Granuloma</term>
<term>Macrophages</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Animals</term>
<term>Female</term>
<term>Humans</term>
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<front><div type="abstract" xml:lang="en">Summary A "hot spot" magnetic resonance (MR) imaging cell tracking technique has been developed that allows direct detection of dysprosium- or thulium-1,4,7,10-tetraazacyclododecane-α,α',α'',α'''-tetramethyl-1,4,7,10-tetraacetic acid (DOTMA)-labeled protons inside cells. These highly shifted protons may allow specific detection of multiple cell types because it does not rely on acquiring the proton signal from bulk water.</div>
</front>
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<Title>Radiology</Title>
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<ArticleTitle>Science to Practice: Highly shifted proton MR imaging--a shift toward better cell tracking?</ArticleTitle>
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<Abstract><AbstractText>Summary A "hot spot" magnetic resonance (MR) imaging cell tracking technique has been developed that allows direct detection of dysprosium- or thulium-1,4,7,10-tetraazacyclododecane-α,α',α'',α'''-tetramethyl-1,4,7,10-tetraacetic acid (DOTMA)-labeled protons inside cells. These highly shifted protons may allow specific detection of multiple cell types because it does not rely on acquiring the proton signal from bulk water.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Bulte</LastName>
<ForeName>Jeff W M</ForeName>
<Initials>JW</Initials>
<AffiliationInfo><Affiliation>Russell H. Morgan Department of Radiology and Radiological Science and Engineering, Division of MR Research, Cellular Imaging Section, Institute for Cell Engineering The Johns Hopkins University School of Medicine 720 Rutland Ave, 217 Traylor Baltimore, MD 21205.</Affiliation>
</AffiliationInfo>
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<Language>eng</Language>
<GrantList CompleteYN="Y"><Grant><GrantID>R01 DA026299</GrantID>
<Acronym>DA</Acronym>
<Agency>NIDA NIH HHS</Agency>
<Country>United States</Country>
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<CommentsCorrectionsList><CommentsCorrections RefType="Cites"><RefSource>Nat Biotechnol. 2005 Aug;23(8):945-6</RefSource>
<PMID Version="1">16082363</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>J Am Chem Soc. 2001 Feb 21;123(7):1517-8</RefSource>
<PMID Version="1">11456734</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Angew Chem Int Ed Engl. 2005 Mar 11;44(12):1813-5</RefSource>
<PMID Version="1">15723362</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Radiology. 2014 Sep;272(3):785-95</RefSource>
<PMID Version="1">24852443</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>FASEB J. 2007 Jun;21(8):1647-54</RefSource>
<PMID Version="1">17284484</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>AJR Am J Roentgenol. 2009 Aug;193(2):314-25</RefSource>
<PMID Version="1">19620426</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Nat Rev Immunol. 2013 Oct;13(10):755-63</RefSource>
<PMID Version="1">24013185</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="CommentOn"><RefSource>Radiology. 2014 Sep;272(3):785-95</RefSource>
<PMID Version="1">24852443</PMID>
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<MeshHeadingList><MeshHeading><DescriptorName MajorTopicYN="N" UI="D000818">Animals</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D058948">Cell Tracking</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D008264">Macrophages</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="Y" UI="D000644">Quaternary Ammonium Compounds</DescriptorName>
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