Literature DB >> 36042312

Aberrant astrocyte protein secretion contributes to altered neuronal development in multiple models of neurodevelopmental disorders.

Laura Sancho1, James Deng1,2, Alexandra Bosworth1,2, Alison L M Caldwell1,2, Audrey Miglietta1, Jolene K Diedrich3, Maxim N Shokhirev4, Nicola J Allen5.   

Abstract

Astrocytes negatively impact neuronal development in many models of neurodevelopmental disorders (NDs); however, how they do this, and if mechanisms are shared across disorders, is not known. In this study, we developed a cell culture system to ask how astrocyte protein secretion and gene expression change in three mouse models of genetic NDs (Rett, Fragile X and Down syndromes). ND astrocytes increase release of Igfbp2, a secreted inhibitor of insulin-like growth factor (IGF). IGF rescues neuronal deficits in many NDs, and we found that blocking Igfbp2 partially rescues inhibitory effects of Rett syndrome astrocytes, suggesting that increased astrocyte Igfbp2 contributes to decreased IGF signaling in NDs. We identified that increased BMP signaling is upstream of protein secretion changes, including Igfbp2, and blocking BMP signaling in Fragile X and Rett syndrome astrocytes reverses inhibitory effects on neurite outgrowth. This work provides a resource of astrocyte-secreted proteins in health and ND models and identifies novel targets for intervention in diverse NDs.
© 2022. The Author(s), under exclusive licence to Springer Nature America, Inc.

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Year:  2022        PMID: 36042312     DOI: 10.1038/s41593-022-01150-1

Source DB:  PubMed          Journal:  Nat Neurosci        ISSN: 1097-6256            Impact factor:   28.771


  65 in total

1.  Control of synapse number by glia.

Authors:  E M Ullian; S K Sapperstein; K S Christopherson; B A Barres
Journal:  Science       Date:  2001-01-26       Impact factor: 47.728

2.  Abnormal development of dendritic spines in FMR1 knock-out mice.

Authors:  E A Nimchinsky; A M Oberlander; K Svoboda
Journal:  J Neurosci       Date:  2001-07-15       Impact factor: 6.167

3.  Neuronal morphology in MeCP2 mouse models is intrinsically variable and depends on age, cell type, and Mecp2 mutation.

Authors:  I-Ting J Wang; Arith-Ruth S Reyes; Zhaolan Zhou
Journal:  Neurobiol Dis       Date:  2013-05-06       Impact factor: 5.996

Review 4.  Role of astrocyte-synapse interactions in CNS disorders.

Authors:  Elena Blanco-Suárez; Alison L M Caldwell; Nicola J Allen
Journal:  J Physiol       Date:  2016-08-08       Impact factor: 5.182

5.  Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2.

Authors:  R E Amir; I B Van den Veyver; M Wan; C Q Tran; U Francke; H Y Zoghbi
Journal:  Nat Genet       Date:  1999-10       Impact factor: 38.330

6.  Trophic interactions between astroglial cells and hippocampal neurons in culture.

Authors:  G A Banker
Journal:  Science       Date:  1980-08-15       Impact factor: 47.728

Review 7.  Autism and the synapse: emerging mechanisms and mechanism-based therapies.

Authors:  Darius Ebrahimi-Fakhari; Mustafa Sahin
Journal:  Curr Opin Neurol       Date:  2015-04       Impact factor: 5.710

Review 8.  On dendrites in Down syndrome and DS murine models: a spiny way to learn.

Authors:  R Benavides-Piccione; I Ballesteros-Yáñez; M Martínez de Lagrán; G Elston; X Estivill; C Fillat; J Defelipe; M Dierssen
Journal:  Prog Neurobiol       Date:  2004-10       Impact factor: 11.685

9.  Non-cell autonomous influence of MeCP2-deficient glia on neuronal dendritic morphology.

Authors:  Nurit Ballas; Daniel T Lioy; Christopher Grunseich; Gail Mandel
Journal:  Nat Neurosci       Date:  2009-02-22       Impact factor: 24.884

Review 10.  Dendritic spine dysgenesis in Rett syndrome.

Authors:  Xin Xu; Eric C Miller; Lucas Pozzo-Miller
Journal:  Front Neuroanat       Date:  2014-09-10       Impact factor: 3.856

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