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Cell Type-Specific In Vitro Gene Expression Profiling of Stem Cell-Derived Neural Models

Genetic and genomic studies of brain disease increasingly demonstrate disease-associated interactions between the cell types of the brain. Increasingly complex and more physiologically relevant human-induced pluripotent stem cell (hiPSC)-based models better explore the molecular mechanisms underlyin...

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Autores principales: Gregory, James A., Hoelzli, Emily, Abdelaal, Rawan, Braine, Catherine, Cuevas, Miguel, Halpern, Madeline, Barretto, Natalie, Schrode, Nadine, Akbalik, Güney, Kang, Kristy, Cheng, Esther, Bowles, Kathryn, Lotz, Steven, Goderie, Susan, Karch, Celeste M., Temple, Sally, Goate, Alison, Brennand, Kristen J., Phatnani, Hemali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7349756/
https://www.ncbi.nlm.nih.gov/pubmed/32516938
http://dx.doi.org/10.3390/cells9061406
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author Gregory, James A.
Hoelzli, Emily
Abdelaal, Rawan
Braine, Catherine
Cuevas, Miguel
Halpern, Madeline
Barretto, Natalie
Schrode, Nadine
Akbalik, Güney
Kang, Kristy
Cheng, Esther
Bowles, Kathryn
Lotz, Steven
Goderie, Susan
Karch, Celeste M.
Temple, Sally
Goate, Alison
Brennand, Kristen J.
Phatnani, Hemali
author_facet Gregory, James A.
Hoelzli, Emily
Abdelaal, Rawan
Braine, Catherine
Cuevas, Miguel
Halpern, Madeline
Barretto, Natalie
Schrode, Nadine
Akbalik, Güney
Kang, Kristy
Cheng, Esther
Bowles, Kathryn
Lotz, Steven
Goderie, Susan
Karch, Celeste M.
Temple, Sally
Goate, Alison
Brennand, Kristen J.
Phatnani, Hemali
author_sort Gregory, James A.
collection PubMed
description Genetic and genomic studies of brain disease increasingly demonstrate disease-associated interactions between the cell types of the brain. Increasingly complex and more physiologically relevant human-induced pluripotent stem cell (hiPSC)-based models better explore the molecular mechanisms underlying disease but also challenge our ability to resolve cell type-specific perturbations. Here, we report an extension of the RiboTag system, first developed to achieve cell type-restricted expression of epitope-tagged ribosomal protein (RPL22) in mouse tissue, to a variety of in vitro applications, including immortalized cell lines, primary mouse astrocytes, and hiPSC-derived neurons. RiboTag expression enables depletion of up to 87 percent of off-target RNA in mixed species co-cultures. Nonetheless, depletion efficiency varies across independent experimental replicates, particularly for hiPSC-derived motor neurons. The challenges and potential of implementing RiboTags in complex in vitro cultures are discussed.
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spelling pubmed-73497562020-07-15 Cell Type-Specific In Vitro Gene Expression Profiling of Stem Cell-Derived Neural Models Gregory, James A. Hoelzli, Emily Abdelaal, Rawan Braine, Catherine Cuevas, Miguel Halpern, Madeline Barretto, Natalie Schrode, Nadine Akbalik, Güney Kang, Kristy Cheng, Esther Bowles, Kathryn Lotz, Steven Goderie, Susan Karch, Celeste M. Temple, Sally Goate, Alison Brennand, Kristen J. Phatnani, Hemali Cells Article Genetic and genomic studies of brain disease increasingly demonstrate disease-associated interactions between the cell types of the brain. Increasingly complex and more physiologically relevant human-induced pluripotent stem cell (hiPSC)-based models better explore the molecular mechanisms underlying disease but also challenge our ability to resolve cell type-specific perturbations. Here, we report an extension of the RiboTag system, first developed to achieve cell type-restricted expression of epitope-tagged ribosomal protein (RPL22) in mouse tissue, to a variety of in vitro applications, including immortalized cell lines, primary mouse astrocytes, and hiPSC-derived neurons. RiboTag expression enables depletion of up to 87 percent of off-target RNA in mixed species co-cultures. Nonetheless, depletion efficiency varies across independent experimental replicates, particularly for hiPSC-derived motor neurons. The challenges and potential of implementing RiboTags in complex in vitro cultures are discussed. MDPI 2020-06-05 /pmc/articles/PMC7349756/ /pubmed/32516938 http://dx.doi.org/10.3390/cells9061406 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Gregory, James A.
Hoelzli, Emily
Abdelaal, Rawan
Braine, Catherine
Cuevas, Miguel
Halpern, Madeline
Barretto, Natalie
Schrode, Nadine
Akbalik, Güney
Kang, Kristy
Cheng, Esther
Bowles, Kathryn
Lotz, Steven
Goderie, Susan
Karch, Celeste M.
Temple, Sally
Goate, Alison
Brennand, Kristen J.
Phatnani, Hemali
Cell Type-Specific In Vitro Gene Expression Profiling of Stem Cell-Derived Neural Models
title Cell Type-Specific In Vitro Gene Expression Profiling of Stem Cell-Derived Neural Models
title_full Cell Type-Specific In Vitro Gene Expression Profiling of Stem Cell-Derived Neural Models
title_fullStr Cell Type-Specific In Vitro Gene Expression Profiling of Stem Cell-Derived Neural Models
title_full_unstemmed Cell Type-Specific In Vitro Gene Expression Profiling of Stem Cell-Derived Neural Models
title_short Cell Type-Specific In Vitro Gene Expression Profiling of Stem Cell-Derived Neural Models
title_sort cell type-specific in vitro gene expression profiling of stem cell-derived neural models
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7349756/
https://www.ncbi.nlm.nih.gov/pubmed/32516938
http://dx.doi.org/10.3390/cells9061406
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