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Intranasal Delivery of Neural Stem/Progenitor Cells: A Noninvasive Passage to Target Intracerebral Glioma

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Intranasal Delivery of Neural Stem/Progenitor Cells: A Noninvasive Passage to Target Intracerebral Glioma

Auteurs : Matthias Reitz ; Maria Demestre ; Jan Sedlacik [Allemagne] ; Hildegard Meissner ; Jens Fiehler [Allemagne] ; Seung U. Kim [Corée du Sud, Canada] ; Manfred Westphal ; Nils Ole Schmidt

Source :

RBID : PMC:3659670

Abstract

This study investigates the feasibility of intranasal administration of neural stem/progenitor cells (NSPCs) as an alternative, noninvasive, and direct passage for the delivery of stem cells to target intracerebral pathologies such as malignant gliomas. Intranasal administration offers the possibility of multiple treatments potentially using tumor-targeting NSPCs with different therapeutic payloads during the disease course.


Url:
DOI: 10.5966/sctm.2012-0045
PubMed: 23283548
PubMed Central: 3659670


Affiliations:


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PMC:3659670

Le document en format XML

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<p>This study investigates the feasibility of intranasal administration of neural stem/progenitor cells (NSPCs) as an alternative, noninvasive, and direct passage for the delivery of stem cells to target intracerebral pathologies such as malignant gliomas. Intranasal administration offers the possibility of multiple treatments potentially using tumor-targeting NSPCs with different therapeutic payloads during the disease course.</p>
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<journal-id journal-id-type="iso-abbrev">Stem Cells Transl Med</journal-id>
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<journal-title-group>
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</journal-title-group>
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<subject>Tissue-Specific Progenitor and Stem Cells</subject>
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<title-group>
<article-title>Intranasal Delivery of Neural Stem/Progenitor Cells: A Noninvasive Passage to Target Intracerebral Glioma</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Reitz</surname>
<given-names>Matthias</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>a</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Demestre</surname>
<given-names>Maria</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>a</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Sedlacik</surname>
<given-names>Jan</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>b</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Meissner</surname>
<given-names>Hildegard</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>a</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Fiehler</surname>
<given-names>Jens</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>b</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Kim</surname>
<given-names>Seung U.</given-names>
</name>
<xref ref-type="aff" rid="aff3">
<sup>c</sup>
</xref>
<xref ref-type="aff" rid="aff4">
<sup>d</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Westphal</surname>
<given-names>Manfred</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>a</sup>
</xref>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Schmidt</surname>
<given-names>Nils Ole</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>a</sup>
</xref>
</contrib>
<aff id="aff1">Departments of
<sup>a</sup>
Neurosurgery and</aff>
<aff id="aff2">
<sup>b</sup>
Neuroradiology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany;</aff>
<aff id="aff3">
<sup>c</sup>
Medical Research Institute, Chung-Ang University College of Medicine, Seoul, Korea;</aff>
<aff id="aff4">
<sup>d</sup>
Division of Neurology, Department of Medicine, University of British Columbia Hospital, Vancouver, British Columbia, Canada</aff>
</contrib-group>
<author-notes>
<corresp>Correspondence: Nils Ole Schmidt, M.D., Department of Neurosurgery, University Medical Center Hamburg-Eppendorf, Martinistrasse 52, 20246 Hamburg, Germany. Telephone:
<phone>49-40-7410-55592</phone>
; Fax:
<fax>49-40-7410-58121</fax>
; E-Mail:
<email>nschmidt@uke.de</email>
</corresp>
</author-notes>
<pub-date pub-type="ppub">
<month>12</month>
<year>2012</year>
</pub-date>
<pub-date pub-type="epub">
<day>27</day>
<month>11</month>
<year>2012</year>
</pub-date>
<volume>1</volume>
<issue>12</issue>
<fpage>866</fpage>
<lpage>873</lpage>
<history>
<date date-type="received">
<day>29</day>
<month>4</month>
<year>2012</year>
</date>
<date date-type="accepted">
<day>13</day>
<month>9</month>
<year>2012</year>
</date>
</history>
<permissions>
<copyright-statement>©AlphaMed Press 1066-5099/2012/$20.00/0</copyright-statement>
<copyright-year>2012</copyright-year>
</permissions>
<self-uri xlink:title="pdf" xlink:type="simple" xlink:href="sct01212000866.pdf"></self-uri>
<abstract abstract-type="precis">
<p>This study investigates the feasibility of intranasal administration of neural stem/progenitor cells (NSPCs) as an alternative, noninvasive, and direct passage for the delivery of stem cells to target intracerebral pathologies such as malignant gliomas. Intranasal administration offers the possibility of multiple treatments potentially using tumor-targeting NSPCs with different therapeutic payloads during the disease course.</p>
</abstract>
<abstract>
<p>Stem cell-based therapies for neurological disorders, including brain tumors, advance continuously toward clinical trials. Optimized cell delivery to the central nervous system remains a challenge since direct intracerebral injection is an invasive method with low transplantation efficiency. We investigated the feasibility of intranasal administration of neural stem/progenitor cells (NSPCs) as an alternative, noninvasive, and direct passage for the delivery of stem cells to target malignant gliomas. Tumor-targeting and migratory pathways of murine and human NSPCs were investigated by intravital magnetic resonance imaging and in histological time course analyses in the intracerebral U87, NCE-G55T2, and syngenic Gl261 glioblastoma models. Intranasally administered NSPCs displayed a rapid, targeted tumor tropism with significant numbers of NSPCs accumulating specifically at the intracerebral glioma site within 6 hours after intranasal delivery. Histological time series analysis revealed that NSPCs migrated within the first 24 hours mainly via olfactory pathways but also by systemic distribution via the microvasculature of the nasal mucosa. Intranasal application of NSPCs leads to a rapid, targeted migration of cells toward intracerebral gliomas. The directional distribution of cells accumulating intra- and peritumorally makes the intranasal delivery of NSPCs a promising noninvasive and convenient alternative delivery method for the treatment of malignant gliomas with the possibility of multiple dosing regimens.</p>
</abstract>
<kwd-group>
<kwd>Cell transplantation</kwd>
<kwd>Clinical translation</kwd>
<kwd>Neural stem cell</kwd>
<kwd>Glioma</kwd>
</kwd-group>
</article-meta>
</front>
</pmc>
<affiliations>
<list>
<country>
<li>Allemagne</li>
<li>Canada</li>
<li>Corée du Sud</li>
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<name sortKey="Reitz, Matthias" sort="Reitz, Matthias" uniqKey="Reitz M" first="Matthias" last="Reitz">Matthias Reitz</name>
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<name sortKey="Westphal, Manfred" sort="Westphal, Manfred" uniqKey="Westphal M" first="Manfred" last="Westphal">Manfred Westphal</name>
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<name sortKey="Fiehler, Jens" sort="Fiehler, Jens" uniqKey="Fiehler J" first="Jens" last="Fiehler">Jens Fiehler</name>
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