http://www.jneurosci.org/content/32/18/6391.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.
No comments:
Post a Comment