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Altered temporal sequence of transcriptional regulators in the generation of human cerebellar granule cells
Brain development is regulated by conserved transcriptional programs across species, but little is known about the divergent mechanisms that create species-specific characteristics. Among brain regions, human cerebellar histogenesis differs in complexity compared with nonhuman primates and rodents,...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8687658/ https://www.ncbi.nlm.nih.gov/pubmed/34842137 http://dx.doi.org/10.7554/eLife.67074 |
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author | Behesti, Hourinaz Kocabas, Arif Buchholz, David E Carroll, Thomas S Hatten, Mary E |
author_facet | Behesti, Hourinaz Kocabas, Arif Buchholz, David E Carroll, Thomas S Hatten, Mary E |
author_sort | Behesti, Hourinaz |
collection | PubMed |
description | Brain development is regulated by conserved transcriptional programs across species, but little is known about the divergent mechanisms that create species-specific characteristics. Among brain regions, human cerebellar histogenesis differs in complexity compared with nonhuman primates and rodents, making it important to develop methods to generate human cerebellar neurons that closely resemble those in the developing human cerebellum. We report a rapid protocol for the derivation of the human ATOH1 lineage, the precursor of excitatory cerebellar neurons, from human pluripotent stem cells (hPSCs). Upon transplantation into juvenile mice, hPSC-derived cerebellar granule cells migrated along glial fibers and integrated into the cerebellar cortex. By Translational Ribosome Affinity Purification-seq, we identified an unexpected temporal shift in the expression of RBFOX3 (NeuN) and NEUROD1, which are classically associated with differentiated neurons, in the human outer external granule layer. This molecular divergence may enable the protracted development of the human cerebellum compared to mice. |
format | Online Article Text |
id | pubmed-8687658 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-86876582021-12-22 Altered temporal sequence of transcriptional regulators in the generation of human cerebellar granule cells Behesti, Hourinaz Kocabas, Arif Buchholz, David E Carroll, Thomas S Hatten, Mary E eLife Developmental Biology Brain development is regulated by conserved transcriptional programs across species, but little is known about the divergent mechanisms that create species-specific characteristics. Among brain regions, human cerebellar histogenesis differs in complexity compared with nonhuman primates and rodents, making it important to develop methods to generate human cerebellar neurons that closely resemble those in the developing human cerebellum. We report a rapid protocol for the derivation of the human ATOH1 lineage, the precursor of excitatory cerebellar neurons, from human pluripotent stem cells (hPSCs). Upon transplantation into juvenile mice, hPSC-derived cerebellar granule cells migrated along glial fibers and integrated into the cerebellar cortex. By Translational Ribosome Affinity Purification-seq, we identified an unexpected temporal shift in the expression of RBFOX3 (NeuN) and NEUROD1, which are classically associated with differentiated neurons, in the human outer external granule layer. This molecular divergence may enable the protracted development of the human cerebellum compared to mice. eLife Sciences Publications, Ltd 2021-11-29 /pmc/articles/PMC8687658/ /pubmed/34842137 http://dx.doi.org/10.7554/eLife.67074 Text en © 2021, Behesti et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Developmental Biology Behesti, Hourinaz Kocabas, Arif Buchholz, David E Carroll, Thomas S Hatten, Mary E Altered temporal sequence of transcriptional regulators in the generation of human cerebellar granule cells |
title | Altered temporal sequence of transcriptional regulators in the generation of human cerebellar granule cells |
title_full | Altered temporal sequence of transcriptional regulators in the generation of human cerebellar granule cells |
title_fullStr | Altered temporal sequence of transcriptional regulators in the generation of human cerebellar granule cells |
title_full_unstemmed | Altered temporal sequence of transcriptional regulators in the generation of human cerebellar granule cells |
title_short | Altered temporal sequence of transcriptional regulators in the generation of human cerebellar granule cells |
title_sort | altered temporal sequence of transcriptional regulators in the generation of human cerebellar granule cells |
topic | Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8687658/ https://www.ncbi.nlm.nih.gov/pubmed/34842137 http://dx.doi.org/10.7554/eLife.67074 |
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