Early response gene induction in astrocytes as a mechanism for encoding and integrating neuronal signals
- PMID: 1363139
- DOI: 10.1016/s0079-6123(08)61749-5
Early response gene induction in astrocytes as a mechanism for encoding and integrating neuronal signals
Abstract
Astrocytes in vitro readily respond to a wide variety of neuronal and systemic signals by inducing a complex pattern of early response genes (ERGs). The level of complexity is evident in both the ligand-associated expression kinetics and levels of message accumulation as well as in the heterogeneity of response within a population of astrocytes. Ligand-restricted expression of ERG mRNAs suggest that all astrocytes in culture are not alike. Although the ability of glial cells to express ERGs appears to be highly restricted in vivo, one important exception is the category of glial response to injury. Long-term expression of multiple ERG proteins in glial cells stimulated by neuropathological conditions may play an important role in the outcome of brain injury and neurodegenerative disease. The extensive and staggered expression of ERG proteins acting as transcription factors may represent a mechanism for temporally coordinating the genomic program of large sets of genes associated with glial cell response to neuronal dysfunction. As part of the neuronal-glial interdependency, glial ERG expression may encode and integrate the environmental signals associated with neuronal damage and promote the proper restoration of neuronal function. For example, ligand-induced ERG expression regulates the transcription of the nerve growth factor (NGF) gene in glia which could have important functional consequences on neuronal survival and process outgrowth. Future studies will clarify the mechanisms that lead to the expression of ERGs and the subsequent complex, temporally ordered combinatorial consequence of numerous ERG proteins acting as transcription factors impinging upon target gene promoters. Such studies will enrich our understanding of astrocyte-neuronal interaction, clarify how distinct sets of genes in glial cells contribute to the problem and/or solution of neuropathological situations and guide our efforts to diagnose and treat neuropathological conditions.
Similar articles
-
Transcriptional and posttranscriptional mechanisms involved in the interleukin-1, steroid, and protein kinase C regulation of nerve growth factor in cortical astrocytes.J Neurochem. 1994 Aug;63(2):419-28. doi: 10.1046/j.1471-4159.1994.63020419.x. J Neurochem. 1994. PMID: 8035171
-
Modulation of prion protein gene expression by growth factors in cultured mouse astrocytes and PC-12 cells.Brain Res Mol Brain Res. 1994 Mar;22(1-4):268-74. doi: 10.1016/0169-328x(94)90055-8. Brain Res Mol Brain Res. 1994. PMID: 7912403
-
Plasticity of astrocytes.Glia. 1994 Jun;11(2):147-55. doi: 10.1002/glia.440110209. Glia. 1994. PMID: 7927644 Review.
-
C-fos induction occurs in cultured cortical neurons and astrocytes via multiple signaling pathways.Prog Brain Res. 1992;94:189-95. doi: 10.1016/s0079-6123(08)61750-1. Prog Brain Res. 1992. PMID: 1337611 No abstract available.
-
Cross-talk signals in the CNS: role of neurotrophic and hormonal factors, adhesion molecules and intercellular signaling agents in luteinizing hormone-releasing hormone (LHRH)-astroglial interactive network.Front Biosci. 1997 Mar 1;2:d88-125. doi: 10.2741/a177. Front Biosci. 1997. PMID: 9159216 Review.
Cited by
-
TNF activates astrocytes and catecholaminergic neurons in the solitary nucleus: implications for autonomic control.Brain Res. 2009 Jun 1;1273:72-82. doi: 10.1016/j.brainres.2009.03.059. Epub 2009 Apr 5. Brain Res. 2009. PMID: 19348788 Free PMC article.
-
Transcriptomic alterations in cortical astrocytes following the development of post-traumatic epilepsy.Sci Rep. 2024 Apr 10;14(1):8367. doi: 10.1038/s41598-024-58904-z. Sci Rep. 2024. PMID: 38600221 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Research Materials