Literature DB >> 28578789

Unravelling and Exploiting Astrocyte Dysfunction in Huntington's Disease.

Baljit S Khakh1, Vahri Beaumont2, Roger Cachope2, Ignacio Munoz-Sanjuan2, Steven A Goldman3, Rosemarie Grantyn4.   

Abstract

Astrocytes are abundant within mature neural circuits and are involved in brain disorders. Here, we summarize our current understanding of astrocytes and Huntington's disease (HD), with a focus on correlative and causative dysfunctions of ion homeostasis, calcium signaling, and neurotransmitter clearance, as well as on the use of transplanted astrocytes to produce therapeutic benefit in mouse models of HD. Overall, the data suggest that astrocyte dysfunction is an important contributor to the onset and progression of some HD symptoms in mice. Additional exploration of astrocytes in HD mouse models and humans is needed and may provide new therapeutic opportunities to explore in conjunction with neuronal rescue and repair strategies.
Copyright © 2017 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  EAAT2; GAT3; GCaMP; GLT1; HD; KCNJ10; Kir4.1; astrocyte; calcium

Mesh:

Year:  2017        PMID: 28578789      PMCID: PMC5706770          DOI: 10.1016/j.tins.2017.05.002

Source DB:  PubMed          Journal:  Trends Neurosci        ISSN: 0166-2236            Impact factor:   13.837


  123 in total

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  54 in total

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7.  Cell Type-Specific Transcriptomics Reveals that Mutant Huntingtin Leads to Mitochondrial RNA Release and Neuronal Innate Immune Activation.

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