Efficient Generation of A9 Midbrain Dopaminergic Neurons by Lentiviral Delivery of LMX1A in Human Embryonic Stem Cells and Induced Pluripotent Stem Cells
Identifieur interne : 001480 ( Main/Merge ); précédent : 001479; suivant : 001481Efficient Generation of A9 Midbrain Dopaminergic Neurons by Lentiviral Delivery of LMX1A in Human Embryonic Stem Cells and Induced Pluripotent Stem Cells
Auteurs : A. Sanchez-Danes [Espagne] ; A. Consiglio [Espagne, Italie] ; Y. Richaud [Espagne] ; I. Rodriguez-Piza [Espagne] ; B. Dehay [Espagne, France] ; M. Edel [Espagne, Australie] ; J. Bove [Espagne] ; M. Memo [Italie] ; M. Vila [Espagne] ; A. Raya [Espagne] ; J. C. Izpisua Belmonte [Espagne, Canada]Source :
- Human gene therapy [ 1043-0342 ] ; 2012.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Homme, Cellule souche.
English descriptors
- KwdEn :
Abstract
Human embryonic stem cells (hESC) and induced pluripotent stem cells (iPSC) offer great hope for in vitro modeling of Parkinson's disease (PD), as well as for designing cell-replacement therapies. To realize these opportunities, there is an urgent need to develop efficient protocols for the directed differentiation of hESC/iPSC into dopamine (DA) neurons with the specific characteristics of the cell population lost to PD, i.e., A9-subtype ventral midbrain DA neurons. Here we use lentiviral vectors to drive the expression of LMX1A, which encodes a transcription factor critical for ventral midbrain identity, specifically in neural progenitor cells. We show that clonal lines of hESC engineered to contain one or two copies of this lentiviral vector retain long-term self-renewing ability and pluripotent differentiation capacity. Greater than 60% of all neurons generated from LMX1A-engineered hESC were ventral midbrain DA neurons of the A9 subtype, compared with ∼10% in green fluorescent protein-engineered controls, as judged by specific marker expression and functional analyses. Moreover, DA neuron precursors differentiated from LMX1A-engineered hESC were able to survive and differentiate when grafted into the brain of adult mice. Finally, we provide evidence that LMX1A overexpression similarly increases the yield of DA neuron differentiation from human iPSC. Taken together, our data show that stable genetic engineering of hESC/iPSC with lentiviral vectors driving controlled expression of LMX1A is an efficient way to generate enriched populations of human A9-subtype ventral midbrain DA neurons, which should prove useful for modeling PD and may be helpful for designing future cell-replacement strategies.
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Pascal:12-0391927Le document en format XML
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Efficient Generation of A9 Midbrain Dopaminergic Neurons by Lentiviral Delivery of LMX1A in Human Embryonic Stem Cells and Induced Pluripotent Stem Cells</title>
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<s2>Barcelona</s2>
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<author><name sortKey="Dehay, B" sort="Dehay, B" uniqKey="Dehay B" first="B." last="Dehay">B. Dehay</name>
<affiliation wicri:level="3"><inist:fA14 i1="06"><s1>Neurodegenerative Diseases Research Group, Vall d'Hebron Research Institute</s1>
<s2>Barcelona</s2>
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<placeName><settlement type="city">Barcelone</settlement>
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<affiliation wicri:level="3"><inist:fA14 i1="08"><s1>Institut des Maladies Neurodégénératives, Université de Bordeaux and CNRS, UMR 5293</s1>
<s2>33000 Bordeaux</s2>
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<affiliation wicri:level="3"><inist:fA14 i1="12"><s1>Visiting Research Fellow at the Victor Chang Cardiac Research Institute</s1>
<s2>Sydney</s2>
<s3>AUS</s3>
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</inist:fA14>
<country>Australie</country>
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<author><name sortKey="Bove, J" sort="Bove, J" uniqKey="Bove J" first="J." last="Bove">J. Bove</name>
<affiliation wicri:level="3"><inist:fA14 i1="04"><s1>Control of Stem Cell Potency Group, Institute for Bioengineering of Catalonia (IBEC)</s1>
<s2>Barcelona</s2>
<s3>ESP</s3>
<sZ>3 aut.</sZ>
<sZ>7 aut.</sZ>
<sZ>10 aut.</sZ>
</inist:fA14>
<country>Espagne</country>
<placeName><settlement type="city">Barcelone</settlement>
<region nuts="2" type="region">Catalogne</region>
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</affiliation>
<affiliation wicri:level="3"><inist:fA14 i1="06"><s1>Neurodegenerative Diseases Research Group, Vall d'Hebron Research Institute</s1>
<s2>Barcelona</s2>
<s3>ESP</s3>
<sZ>5 aut.</sZ>
<sZ>7 aut.</sZ>
<sZ>9 aut.</sZ>
</inist:fA14>
<country>Espagne</country>
<placeName><settlement type="city">Barcelone</settlement>
<region nuts="2" type="region">Catalogne</region>
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</author>
<author><name sortKey="Memo, M" sort="Memo, M" uniqKey="Memo M" first="M." last="Memo">M. Memo</name>
<affiliation wicri:level="1"><inist:fA14 i1="03"><s1>Department of Biomedical Science and Biotechnology, University of Brescia</s1>
<s2>Brescia</s2>
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<affiliation wicri:level="3"><inist:fA14 i1="06"><s1>Neurodegenerative Diseases Research Group, Vall d'Hebron Research Institute</s1>
<s2>Barcelona</s2>
<s3>ESP</s3>
<sZ>5 aut.</sZ>
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<country>Espagne</country>
<placeName><settlement type="city">Barcelone</settlement>
<region nuts="2" type="region">Catalogne</region>
</placeName>
</affiliation>
<affiliation wicri:level="3"><inist:fA14 i1="07"><s1>Networking Center of Biomedical Research on Neurodegenerative Diseases (CIBERNED)</s1>
<s2>Barcelona</s2>
<s3>ESP</s3>
<sZ>5 aut.</sZ>
<sZ>9 aut.</sZ>
</inist:fA14>
<country>Espagne</country>
<placeName><settlement type="city">Barcelone</settlement>
<region nuts="2" type="region">Catalogne</region>
</placeName>
</affiliation>
<affiliation wicri:level="3"><inist:fA14 i1="10"><s1>Catalan Institution for Research and Advanced Studies (ICREA)</s1>
<s2>Barcelona</s2>
<s3>ESP</s3>
<sZ>9 aut.</sZ>
<sZ>10 aut.</sZ>
</inist:fA14>
<country>Espagne</country>
<placeName><settlement type="city">Barcelone</settlement>
<region nuts="2" type="region">Catalogne</region>
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</affiliation>
</author>
<author><name sortKey="Raya, A" sort="Raya, A" uniqKey="Raya A" first="A." last="Raya">A. Raya</name>
<affiliation wicri:level="3"><inist:fA14 i1="04"><s1>Control of Stem Cell Potency Group, Institute for Bioengineering of Catalonia (IBEC)</s1>
<s2>Barcelona</s2>
<s3>ESP</s3>
<sZ>3 aut.</sZ>
<sZ>7 aut.</sZ>
<sZ>10 aut.</sZ>
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<s2>Barcelona</s2>
<s3>ESP</s3>
<sZ>3 aut.</sZ>
<sZ>10 aut.</sZ>
</inist:fA14>
<country>Espagne</country>
<placeName><settlement type="city">Barcelone</settlement>
<region nuts="2" type="region">Catalogne</region>
</placeName>
</affiliation>
<affiliation wicri:level="3"><inist:fA14 i1="10"><s1>Catalan Institution for Research and Advanced Studies (ICREA)</s1>
<s2>Barcelona</s2>
<s3>ESP</s3>
<sZ>9 aut.</sZ>
<sZ>10 aut.</sZ>
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<country>Espagne</country>
<placeName><settlement type="city">Barcelone</settlement>
<region nuts="2" type="region">Catalogne</region>
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<author><name sortKey="Izpisua Belmonte, J C" sort="Izpisua Belmonte, J C" uniqKey="Izpisua Belmonte J" first="J. C." last="Izpisua Belmonte">J. C. Izpisua Belmonte</name>
<affiliation wicri:level="3"><inist:fA14 i1="02"><s1>Center for Regenerative Medicine in Barcelona</s1>
<s2>Barcelona</s2>
<s3>ESP</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>11 aut.</sZ>
</inist:fA14>
<country>Espagne</country>
<placeName><settlement type="city">Barcelone</settlement>
<region nuts="2" type="region">Catalogne</region>
</placeName>
</affiliation>
<affiliation wicri:level="1"><inist:fA14 i1="11"><s1>Gene Expression Laboratory, Salk Institute for Biological Studies</s1>
<s2>La Jolla</s2>
<s3>CAN</s3>
<sZ>11 aut.</sZ>
</inist:fA14>
<country>Canada</country>
<wicri:noRegion>La Jolla</wicri:noRegion>
</affiliation>
</author>
</analytic>
<series><title level="j" type="main">Human gene therapy</title>
<title level="j" type="abbreviated">Hum. gene ther.</title>
<idno type="ISSN">1043-0342</idno>
<imprint><date when="2012">2012</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt><title level="j" type="main">Human gene therapy</title>
<title level="j" type="abbreviated">Hum. gene ther.</title>
<idno type="ISSN">1043-0342</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Embryonic cell</term>
<term>Gene therapy</term>
<term>Human</term>
<term>Induced pluripotent stem cell</term>
<term>Lentivirus</term>
<term>Midbrain</term>
<term>Neuron</term>
<term>Stem cell</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Mésencéphale</term>
<term>Neurone</term>
<term>Homme</term>
<term>Cellule embryonnaire</term>
<term>Cellule souche</term>
<term>Thérapie génique</term>
<term>Lentivirus</term>
<term>Cellule souche pluripotente induite</term>
</keywords>
<keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Homme</term>
<term>Cellule souche</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">Human embryonic stem cells (hESC) and induced pluripotent stem cells (iPSC) offer great hope for in vitro modeling of Parkinson's disease (PD), as well as for designing cell-replacement therapies. To realize these opportunities, there is an urgent need to develop efficient protocols for the directed differentiation of hESC/iPSC into dopamine (DA) neurons with the specific characteristics of the cell population lost to PD, i.e., A9-subtype ventral midbrain DA neurons. Here we use lentiviral vectors to drive the expression of LMX1A, which encodes a transcription factor critical for ventral midbrain identity, specifically in neural progenitor cells. We show that clonal lines of hESC engineered to contain one or two copies of this lentiviral vector retain long-term self-renewing ability and pluripotent differentiation capacity. Greater than 60% of all neurons generated from LMX1A-engineered hESC were ventral midbrain DA neurons of the A9 subtype, compared with ∼10% in green fluorescent protein-engineered controls, as judged by specific marker expression and functional analyses. Moreover, DA neuron precursors differentiated from LMX1A-engineered hESC were able to survive and differentiate when grafted into the brain of adult mice. Finally, we provide evidence that LMX1A overexpression similarly increases the yield of DA neuron differentiation from human iPSC. Taken together, our data show that stable genetic engineering of hESC/iPSC with lentiviral vectors driving controlled expression of LMX1A is an efficient way to generate enriched populations of human A9-subtype ventral midbrain DA neurons, which should prove useful for modeling PD and may be helpful for designing future cell-replacement strategies.</div>
</front>
</TEI>
<affiliations><list><country><li>Australie</li>
<li>Canada</li>
<li>Espagne</li>
<li>France</li>
<li>Italie</li>
</country>
<region><li>Aquitaine</li>
<li>Catalogne</li>
<li>Nouvelle-Aquitaine</li>
</region>
<settlement><li>Barcelone</li>
<li>Bordeaux</li>
<li>Sydney</li>
</settlement>
</list>
<tree><country name="Espagne"><region name="Catalogne"><name sortKey="Sanchez Danes, A" sort="Sanchez Danes, A" uniqKey="Sanchez Danes A" first="A." last="Sanchez-Danes">A. Sanchez-Danes</name>
</region>
<name sortKey="Bove, J" sort="Bove, J" uniqKey="Bove J" first="J." last="Bove">J. Bove</name>
<name sortKey="Bove, J" sort="Bove, J" uniqKey="Bove J" first="J." last="Bove">J. Bove</name>
<name sortKey="Consiglio, A" sort="Consiglio, A" uniqKey="Consiglio A" first="A." last="Consiglio">A. Consiglio</name>
<name sortKey="Consiglio, A" sort="Consiglio, A" uniqKey="Consiglio A" first="A." last="Consiglio">A. Consiglio</name>
<name sortKey="Dehay, B" sort="Dehay, B" uniqKey="Dehay B" first="B." last="Dehay">B. Dehay</name>
<name sortKey="Dehay, B" sort="Dehay, B" uniqKey="Dehay B" first="B." last="Dehay">B. Dehay</name>
<name sortKey="Edel, M" sort="Edel, M" uniqKey="Edel M" first="M." last="Edel">M. Edel</name>
<name sortKey="Izpisua Belmonte, J C" sort="Izpisua Belmonte, J C" uniqKey="Izpisua Belmonte J" first="J. C." last="Izpisua Belmonte">J. C. Izpisua Belmonte</name>
<name sortKey="Raya, A" sort="Raya, A" uniqKey="Raya A" first="A." last="Raya">A. Raya</name>
<name sortKey="Raya, A" sort="Raya, A" uniqKey="Raya A" first="A." last="Raya">A. Raya</name>
<name sortKey="Raya, A" sort="Raya, A" uniqKey="Raya A" first="A." last="Raya">A. Raya</name>
<name sortKey="Richaud, Y" sort="Richaud, Y" uniqKey="Richaud Y" first="Y." last="Richaud">Y. Richaud</name>
<name sortKey="Richaud, Y" sort="Richaud, Y" uniqKey="Richaud Y" first="Y." last="Richaud">Y. Richaud</name>
<name sortKey="Rodriguez Piza, I" sort="Rodriguez Piza, I" uniqKey="Rodriguez Piza I" first="I." last="Rodriguez-Piza">I. Rodriguez-Piza</name>
<name sortKey="Sanchez Danes, A" sort="Sanchez Danes, A" uniqKey="Sanchez Danes A" first="A." last="Sanchez-Danes">A. Sanchez-Danes</name>
<name sortKey="Vila, M" sort="Vila, M" uniqKey="Vila M" first="M." last="Vila">M. Vila</name>
<name sortKey="Vila, M" sort="Vila, M" uniqKey="Vila M" first="M." last="Vila">M. Vila</name>
<name sortKey="Vila, M" sort="Vila, M" uniqKey="Vila M" first="M." last="Vila">M. Vila</name>
</country>
<country name="Italie"><noRegion><name sortKey="Consiglio, A" sort="Consiglio, A" uniqKey="Consiglio A" first="A." last="Consiglio">A. Consiglio</name>
</noRegion>
<name sortKey="Memo, M" sort="Memo, M" uniqKey="Memo M" first="M." last="Memo">M. Memo</name>
</country>
<country name="France"><region name="Nouvelle-Aquitaine"><name sortKey="Dehay, B" sort="Dehay, B" uniqKey="Dehay B" first="B." last="Dehay">B. Dehay</name>
</region>
</country>
<country name="Australie"><noRegion><name sortKey="Edel, M" sort="Edel, M" uniqKey="Edel M" first="M." last="Edel">M. Edel</name>
</noRegion>
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</noRegion>
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</tree>
</affiliations>
</record>
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