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dc.contributor.authorHuang, Ting-Hao
dc.contributor.authorVelho, Tarciso
dc.contributor.authorLois, Carlos
dc.date2022-08-11T08:09:29.000
dc.date.accessioned2022-08-23T16:32:36Z
dc.date.available2022-08-23T16:32:36Z
dc.date.issued2016-11-01
dc.date.submitted2016-11-07
dc.identifier.citationDevelopment. 2016 Nov 1;143(21):4073-4084. Epub 2016 Sep 22. <a href="http://dx.doi.org/10.1242/dev.142406">Link to article on publisher's site</a>
dc.identifier.issn0950-1991 (Linking)
dc.identifier.doi10.1242/dev.142406
dc.identifier.pmid27660327
dc.identifier.urihttp://hdl.handle.net/20.500.14038/37918
dc.description<p>Ting-Hao Huang is a doctoral student in the Neuroscience Program in the Graduate School of Biomedical Sciences at UMass Medical School.</p>
dc.description.abstractWe used a synthetic genetic system based on ligand-induced intramembrane proteolysis to monitor cell-cell contacts in animals. Upon ligand-receptor interaction in sites of cell-cell contact, the transmembrane domain of an engineered receptor is cleaved by intramembrane proteolysis and releases a protein fragment that regulates transcription in the interacting partners. We demonstrate that the system can be used to regulate gene expression between interacting cells, both in vitro and in vivo, in transgenic Drosophila We show that the system allows for detection of interactions between neurons and glia in the Drosophila nervous system. In addition, we observed that when the ligand is expressed in subsets of neurons with a restricted localization in the brain it leads to activation of transcription in a selected set of glial cells that interact with those neurons. This system will be useful to monitor cell-cell interactions in animals, and can be used to genetically manipulate cells that interact with one another.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=27660327&dopt=Abstract">Link to Article in PubMed</a>
dc.rightsPublisher PDF posted after 12 months as allowed by publisher's author rights policy at http://dev.biologists.org/content/rights-permissions.
dc.subjectAdhesion
dc.subjectCell communication
dc.subjectDevelopment
dc.subjectInteracting cells
dc.subjectMorphogenesis
dc.subjectCell Biology
dc.subjectDevelopmental Biology
dc.subjectDevelopmental Neuroscience
dc.titleMonitoring cell-cell contacts in vivo in transgenic animals
dc.typeJournal Article
dc.source.journaltitleDevelopment (Cambridge, England)
dc.source.volume143
dc.source.issue21
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=1189&amp;context=neurobiology_pp&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/neurobiology_pp/190
dc.legacy.embargo2017-11-01T00:00:00-07:00
dc.identifier.contextkey9353514
refterms.dateFOA2022-08-23T16:32:36Z
html.description.abstract<p>We used a synthetic genetic system based on ligand-induced intramembrane proteolysis to monitor cell-cell contacts in animals. Upon ligand-receptor interaction in sites of cell-cell contact, the transmembrane domain of an engineered receptor is cleaved by intramembrane proteolysis and releases a protein fragment that regulates transcription in the interacting partners. We demonstrate that the system can be used to regulate gene expression between interacting cells, both in vitro and in vivo, in transgenic Drosophila We show that the system allows for detection of interactions between neurons and glia in the Drosophila nervous system. In addition, we observed that when the ligand is expressed in subsets of neurons with a restricted localization in the brain it leads to activation of transcription in a selected set of glial cells that interact with those neurons. This system will be useful to monitor cell-cell interactions in animals, and can be used to genetically manipulate cells that interact with one another.</p>
dc.identifier.submissionpathneurobiology_pp/190
dc.contributor.departmentGraduate School of Biomedical Sciences, Neuroscience Program
dc.contributor.departmentLois Lab
dc.contributor.departmentNeurobiology
dc.source.pages4073-4084


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