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Journal of Neuroscience· 2012Q1

Genomic Analysis of Reactive Astrogliosis

Jennifer Zamanian, Lijun Xu, Lynette C. Foo, Navid Nouri et al.

Short summary

Reactive astrocytes, crucial for CNS injury response, exhibit distinct molecular phenotypes depending on the specific injury type, with at least 50% of gene expression changes being injury-specific.

AI-generated from the title and abstract; the full text is not read.

Key points

  • Reactive astrogliosis involves rapid but transient gene expression changes after CNS injury.
  • Lcn2 and Serpina3n are identified as strong molecular markers for reactive astrocytes.
  • Over 50% of gene expression changes in reactive astrocytes are specific to the injury type (ischemia vs. neuroinflammation).
  • Astrocyte phenotype in ischemia suggests a protective role, while in LPS-induced inflammation, it suggests a detrimental role.

AI-generated from the title and abstract; the full text is not read.

Abstract

Reactive astrogliosis is characterized by a profound change in astrocyte phenotype in response to all CNS injuries and diseases. To better understand the reactive astrocyte state, we used Affymetrix GeneChip arrays to profile gene expression in populations of reactive astrocytes isolated at various time points after induction using two mouse injury models, ischemic stroke and neuroinflammation. We find reactive gliosis consists of a rapid, but quickly attenuated, induction of gene expression after insult and identify induced Lcn2 and Serpina3n as strong markers of reactive astrocytes. Strikingly, reactive astrocyte phenotype strongly depended on the type of inducing injury. Although there is a core set of genes that is upregulated in reactive astrocytes from both injury models, at least 50% of the altered gene expression is specific to a given injury type. Reactive astrocytes in ischemia exhibited a molecular phenotype that suggests that they may be beneficial or protective, whereas reactive astrocytes induced by LPS exhibited a phenotype that suggests that they may be detrimental. These findings demonstrate that, despite well established commonalities, astrocyte reactive gliosis is a highly heterogeneous state in which astrocyte activities are altered to respond to the specific injury. This raises the question of how many subtypes of reactive astrocytes exist. Our findings provide transcriptome databases for two subtypes of reactive astrocytes that will be highly useful in generating new and testable hypotheses of their function, as well as for providing new markers to detect different types of reactive astrocytes in human neurological diseases.

The authors' abstract, as published at the source. Journal of Neuroscience, 2012 · DOI ↗

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Field: Neurology (Neuroscience)

NeurologyNeuroscience