Human Brain Organoids to Decode Mechanisms of Microcephaly

Brain organoids are stem cell-based self-assembling 3D structures that recapitulate early events of human brain development. Recent improvements with patient-specific 3D brain organoids have begun to elucidate unprecedented details of the defective mechanisms that cause neurodevelopmental disorders...

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Main Authors: Elke Gabriel, Anand Ramani, Nazlican Altinisik, Jay Gopalakrishnan
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-05-01
Series:Frontiers in Cellular Neuroscience
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fncel.2020.00115/full
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spelling doaj-a7bd891fede04150a9fb6ca4c7c1c4252020-11-25T03:16:55ZengFrontiers Media S.A.Frontiers in Cellular Neuroscience1662-51022020-05-011410.3389/fncel.2020.00115532477Human Brain Organoids to Decode Mechanisms of MicrocephalyElke GabrielAnand RamaniNazlican AltinisikJay GopalakrishnanBrain organoids are stem cell-based self-assembling 3D structures that recapitulate early events of human brain development. Recent improvements with patient-specific 3D brain organoids have begun to elucidate unprecedented details of the defective mechanisms that cause neurodevelopmental disorders of congenital and acquired microcephaly. In particular, brain organoids derived from primary microcephaly patients have uncovered mechanisms that deregulate neural stem cell proliferation, maintenance, and differentiation. Not only did brain organoids reveal unknown aspects of neurogenesis but also have illuminated surprising roles of cellular structures of centrosomes and primary cilia in regulating neurogenesis during brain development. Here, we discuss how brain organoids have started contributing to decoding the complexities of microcephaly, which are unlikely to be identified in the existing non-human models. Finally, we discuss the yet unresolved questions and challenges that can be addressed with the use of brain organoids as in vitro models of neurodevelopmental disorders.https://www.frontiersin.org/article/10.3389/fncel.2020.00115/fullcentrosomesprimary cilianeural progenitor cells (NPCs)induced pluripotent stem cells (iPSCs)human brain organoidsmicrocephaly
collection DOAJ
language English
format Article
sources DOAJ
author Elke Gabriel
Anand Ramani
Nazlican Altinisik
Jay Gopalakrishnan
spellingShingle Elke Gabriel
Anand Ramani
Nazlican Altinisik
Jay Gopalakrishnan
Human Brain Organoids to Decode Mechanisms of Microcephaly
Frontiers in Cellular Neuroscience
centrosomes
primary cilia
neural progenitor cells (NPCs)
induced pluripotent stem cells (iPSCs)
human brain organoids
microcephaly
author_facet Elke Gabriel
Anand Ramani
Nazlican Altinisik
Jay Gopalakrishnan
author_sort Elke Gabriel
title Human Brain Organoids to Decode Mechanisms of Microcephaly
title_short Human Brain Organoids to Decode Mechanisms of Microcephaly
title_full Human Brain Organoids to Decode Mechanisms of Microcephaly
title_fullStr Human Brain Organoids to Decode Mechanisms of Microcephaly
title_full_unstemmed Human Brain Organoids to Decode Mechanisms of Microcephaly
title_sort human brain organoids to decode mechanisms of microcephaly
publisher Frontiers Media S.A.
series Frontiers in Cellular Neuroscience
issn 1662-5102
publishDate 2020-05-01
description Brain organoids are stem cell-based self-assembling 3D structures that recapitulate early events of human brain development. Recent improvements with patient-specific 3D brain organoids have begun to elucidate unprecedented details of the defective mechanisms that cause neurodevelopmental disorders of congenital and acquired microcephaly. In particular, brain organoids derived from primary microcephaly patients have uncovered mechanisms that deregulate neural stem cell proliferation, maintenance, and differentiation. Not only did brain organoids reveal unknown aspects of neurogenesis but also have illuminated surprising roles of cellular structures of centrosomes and primary cilia in regulating neurogenesis during brain development. Here, we discuss how brain organoids have started contributing to decoding the complexities of microcephaly, which are unlikely to be identified in the existing non-human models. Finally, we discuss the yet unresolved questions and challenges that can be addressed with the use of brain organoids as in vitro models of neurodevelopmental disorders.
topic centrosomes
primary cilia
neural progenitor cells (NPCs)
induced pluripotent stem cells (iPSCs)
human brain organoids
microcephaly
url https://www.frontiersin.org/article/10.3389/fncel.2020.00115/full
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AT nazlicanaltinisik humanbrainorganoidstodecodemechanismsofmicrocephaly
AT jaygopalakrishnan humanbrainorganoidstodecodemechanismsofmicrocephaly
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