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Zeb2 Is a Regulator of Astrogliosis and Functional Recovery after CNS Injury.


ABSTRACT: The astrocytic response to injury is characterized on the cellular level, but our understanding of the molecular mechanisms controlling the cellular processes is incomplete. The astrocytic response to injury is similar to wound-healing responses in non-neural tissues that involve epithelial-to-mesenchymal transitions (EMTs) and upregulation in ZEB transcription factors. Here we show that injury-induced astrogliosis increases EMT-related genes expression, including Zeb2, and long non-coding RNAs, including Zeb2os, which facilitates ZEB2 protein translation. In mouse models of either contusive spinal cord injury or transient ischemic stroke, the conditional knockout of Zeb2 in astrocytes attenuates astrogliosis, generates larger lesions, and delays the recovery of motor function. These findings reveal ZEB2 as an important regulator of the astrocytic response to injury and suggest that astrogliosis is an EMT-like process, which provides a conceptual connection for the molecular and cellular similarities between astrogliosis and wound-healing responses in non-neural tissue.

SUBMITTER: Vivinetto AL 

PROVIDER: S-EPMC7416489 | biostudies-literature | 2020 Jun

REPOSITORIES: biostudies-literature

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Zeb2 Is a Regulator of Astrogliosis and Functional Recovery after CNS Injury.

Vivinetto Ana L AL   Kim Il-Doo ID   Goldberg David C DC   Fones Lilah L   Brown Elizabeth E   Tarabykin Victor S VS   Hill Caitlin E CE   Cho Sunghee S   Cave John W JW  

Cell reports 20200601 13


The astrocytic response to injury is characterized on the cellular level, but our understanding of the molecular mechanisms controlling the cellular processes is incomplete. The astrocytic response to injury is similar to wound-healing responses in non-neural tissues that involve epithelial-to-mesenchymal transitions (EMTs) and upregulation in ZEB transcription factors. Here we show that injury-induced astrogliosis increases EMT-related genes expression, including Zeb2, and long non-coding RNAs,  ...[more]

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