Senescent and reactive astrocytes display distinct expression profiles and divergent functional capacities.

Abstract

Astrocytes assume multiple phenotypes in the brain in response to stress, injury, inflammation, and aging. Given the complexity of this critical cell type in the CNS, it is important to gain a greater understanding of the differences between these phenotypes and to potentially identify therapeutic approaches to modifying astrocyte function in the context of disease and aging. We compared senescent and reactive astrocytes using a strictly defined paradigm to induce these phenotypes in human astrocytes. Gene expression profiling reveals overlapping but distinct expression profiles. Reactive astrocytes predominantly express genes involved in inflammatory responses while senescent astrocytes express genes and a secretome that suggests a role in synaptic pruning. Unexpectedly, functional analysis in a simplified neurite outgrowth assay suggests that senescent astrocytes retain the ability to support neurite outgrowth while reactive astrocytes lose this capacity. The data suggests that senescent and reactive astrocytes play distinct functional roles in the physiology of the aging brain. However, the overlapping inflammatory nature of senescent and reactive astrocytes makes it difficult to discriminate between them using existing toolsets designed to identify senescent cells.