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

被引:2
作者
Gregory, James A. [1 ]
Hoelzli, Emily [1 ]
Abdelaal, Rawan [1 ]
Braine, Catherine [2 ]
Cuevas, Miguel [2 ]
Halpern, Madeline [3 ]
Barretto, Natalie [3 ]
Schrode, Nadine [3 ]
Akbalik, Guney [1 ]
Kang, Kristy [1 ]
Cheng, Esther [3 ]
Bowles, Kathryn [4 ]
Lotz, Steven [5 ]
Goderie, Susan [5 ]
Karch, Celeste M. [6 ]
Temple, Sally [5 ]
Goate, Alison [4 ]
Brennand, Kristen J. [3 ]
Phatnani, Hemali [1 ,2 ]
机构
[1] New York Genome Ctr, Ctr Genom Neurodegenerat Dis, New York, NY 10013 USA
[2] Columbia Univ, Dept Neurol, Med Ctr, New York, NY 10068 USA
[3] Icahn Sch Med Mt Sinai, Dept Genet & Genom, Pamela Sklar Div Psychiat Genom, New York, NY 10029 USA
[4] Icahn Sch Med Mt Sinai, Dept Neurosci, Ronald M Loeb Ctr Alzheimers Dis, New York, NY 10029 USA
[5] Neural Stem Cell Inst, One Discovery Dr, Rensselaer, NY 12144 USA
[6] Washington Univ, Dept Psychiat, St Louis, MO 63110 USA
基金
美国国家卫生研究院;
关键词
hiPSC; neuron; glia; RiboTag; bacTRAP; genomics; RNA-seq; MESSENGER-RNA-SEQ; TRANSCRIPTOME ANALYSIS; IDENTIFICATION; NEURONS; EPITOPE; PURIFICATION; PROTEINS; COMPLEX; RIBOTAG;
D O I
10.3390/cells9061406
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页码:1 / 18
页数:18
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