Literature DB >> 31742552

Cerebellar nuclei excitatory neurons regulate developmental scaling of presynaptic Purkinje cell number and organ growth.

Ryan T Willett1, N Sumru Bayin1, Andrew S Lee1,2, Anjana Krishnamurthy1,2, Alexandre Wojcinski1, Zhimin Lao1, Daniel Stephen1, Alberto Rosello-Diez1, Katherine L Dauber-Decker1, Grant D Orvis1, Zhuhao Wu3, Marc Tessier-Lavigne3, Alexandra L Joyner1,2,4.   

Abstract

For neural systems to function effectively, the numbers of each cell type must be proportioned properly during development. We found that conditional knockout of the mouse homeobox genes En1 and En2 in the excitatory cerebellar nuclei neurons (eCN) leads to reduced postnatal growth of the cerebellar cortex. A subset of medial and intermediate eCN are lost in the mutants, with an associated cell non-autonomous loss of their presynaptic partner Purkinje cells by birth leading to proportional scaling down of neuron production in the postnatal cerebellar cortex. Genetic killing of embryonic eCN throughout the cerebellum also leads to loss of Purkinje cells and reduced postnatal growth but throughout the cerebellar cortex. Thus, the eCN play a key role in scaling the size of the cerebellum by influencing the survival of their Purkinje cell partners, which in turn regulate production of granule cells and interneurons via the amount of sonic hedgehog secreted.
© 2019, Willett et al.

Entities:  

Keywords:  SHH; conditional mutants; developmental biology; engrailed genes; granule cells; interneurons; mouse; neuroscience

Mesh:

Substances:

Year:  2019        PMID: 31742552      PMCID: PMC6890462          DOI: 10.7554/eLife.50617

Source DB:  PubMed          Journal:  Elife        ISSN: 2050-084X            Impact factor:   8.140


  57 in total

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2.  Heterogeneity and Bipotency of Astroglial-Like Cerebellar Progenitors along the Interneuron and Glial Lineages.

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3.  The interconnection between the vestibular nuclei and the nodulus: a study of reciprocity.

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Authors:  W D Snider
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8.  The engrailed homeobox genes are required in multiple cell lineages to coordinate sequential formation of fissures and growth of the cerebellum.

Authors:  Grant D Orvis; Andrea L Hartzell; Jenessa B Smith; Luis Humberto Barraza; Sandra L Wilson; Kamila U Szulc; Daniel H Turnbull; Alexandra L Joyner
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Authors:  K J Millen; C C Hui; A L Joyner
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  12 in total

1.  A collection of genetic mouse lines and related tools for inducible and reversible intersectional mis-expression.

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Review 2.  Human Cerebellar Development and Transcriptomics: Implications for Neurodevelopmental Disorders.

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4.  Common Origin of the Cerebellar Dual Somatotopic Areas Revealed by Tracking Embryonic Purkinje Cell Clusters with Birthdate Tagging.

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Review 5.  Interactions Between Purkinje Cells and Granule Cells Coordinate the Development of Functional Cerebellar Circuits.

Authors:  Meike E van der Heijden; Roy V Sillitoe
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6.  Conditional loss of Engrailed1/2 in Atoh1-derived excitatory cerebellar nuclear neurons impairs eupneic respiration in mice.

Authors:  Angela P Taylor; Andrew S Lee; Patricia J Goedecke; Elizabeth A Tolley; Alexandra L Joyner; Detlef H Heck
Journal:  Genes Brain Behav       Date:  2022-01-19       Impact factor: 3.449

Review 7.  Transcriptome programs involved in the development and structure of the cerebellum.

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8.  EN1 Regulates Cell Growth and Proliferation in Human Glioma Cells via Hedgehog Signaling.

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9.  Single-cell spatial transcriptomic analysis reveals common and divergent features of developing postnatal granule cerebellar cells and medulloblastoma.

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10.  Longitudinal MEMRI analysis of brain phenotypes in a mouse model of Niemann-Pick Type C disease.

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