Nature CommunicationsNeurosciencePeer-reviewed journal article
Extensive transcriptional and chromatin changes underlie astrocyte maturation in vivo and in culture
Michael LattkeiD, Robert J. GoldstoneiD, James K. EllisiD, Stefan BoeingiD, Jerónimo Jurado‐ArjonaiD, Nicolás MarichaliD, James I. MacRaeiD, Benedikt BerningeriD, François GuillemotiD
Abstract
Astrocytes have diverse functions in brain homeostasis. Many of these functions are acquired during late stages of differentiation when astrocytes become fully mature. The mechanisms underlying astrocyte maturation are not well understood. Here we identified extensive transcriptional changes that occur during astrocyte maturation and are accompanied by chromatin remodelling at enhancer elements. Investigating astrocyte maturation in a cell culture model revealed that in vitro-differentiated astrocytes lacked expression of many mature astrocyte-specific genes, including genes for the transcription factors Rorb, Dbx2, Lhx2 and Fezf2. Forced expression of these factors in vitro induced distinct sets of mature astrocytes-specific transcripts. Culturing astrocytes with FGF2 in a three-dimensional gel induced expression of Rorb, Dbx2 and Lhx2 and improved their maturity based on transcriptional and chromatin profiles. Therefore extrinsic signals orchestrate the expression of multiple intrinsic regulators, which in turn induce in a modular manner the transcriptional and chromatin changes underlying astrocyte maturation.
- organism: mouse
- assay: bulk RNA-seq
- assay: ChIP-seq
- research focus: cell type annotation
- research focus: differential expression
- research focus: gene regulatory network inference
- approach: statistical model
- approach: experimental assay
- Citations
- 111
- FWCI
- 6.14
- Field percentile
- top 2%
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