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Comparative genomic analysis of embryonic, lineage-converted and stem cell-derived motor neurons.

Authors :
Ichida JK
Staats KA
Davis-Dusenbery BN
Clement K
Galloway KE
Babos KN
Shi Y
Son EY
Kiskinis E
Atwater N
Gu H
Gnirke A
Meissner A
Eggan K
Source :
Development (Cambridge, England) [Development] 2018 Nov 21; Vol. 145 (22). Date of Electronic Publication: 2018 Nov 21.
Publication Year :
2018

Abstract

Advances in stem cell science allow the production of different cell types in vitro either through the recapitulation of developmental processes, often termed 'directed differentiation', or the forced expression of lineage-specific transcription factors. Although cells produced by both approaches are increasingly used in translational applications, their quantitative similarity to their primary counterparts remains largely unresolved. To investigate the similarity between in vitro -derived and primary cell types, we harvested and purified mouse spinal motor neurons and compared them with motor neurons produced by transcription factor-mediated lineage conversion of fibroblasts or directed differentiation of pluripotent stem cells. To enable unbiased analysis of these motor neuron types and their cells of origin, we then subjected them to whole transcriptome and DNA methylome analysis by RNA sequencing (RNA-seq) and reduced representation bisulfite sequencing (RRBS). Despite major differences in methodology, lineage conversion and directed differentiation both produce cells that closely approximate the primary motor neuron state. However, we identify differences in Fas signaling, the Hox code and synaptic gene expression between lineage-converted and directed differentiation motor neurons that affect their utility in translational studies.<br />Competing Interests: Competing interestsJ.K.I. is a co-founder of AcuraStem. K.E. is a co-founder of Q-State Biosciences and QurAlis.<br /> (© 2018. Published by The Company of Biologists Ltd.)

Details

Language :
English
ISSN :
1477-9129
Volume :
145
Issue :
22
Database :
MEDLINE
Journal :
Development (Cambridge, England)
Publication Type :
Academic Journal
Accession number :
30337375
Full Text :
https://doi.org/10.1242/dev.168617