Chronic stress from adolescence to aging in the prefrontal cortex: A neuroimmune perspective

Front Neuroendocrinol. 2018 Apr:49:31-42. doi: 10.1016/j.yfrne.2017.12.001. Epub 2017 Dec 16.

Abstract

The development of the organism is a critical variable which influences the magnitude, duration, and reversibility of the effects of chronic stress. Such factors are relevant to the prefrontal cortex (PFC), as this brain region is the last to mature, the first to decline, and is highly stress-sensitive. Therefore, this review will examine the intersection between the nervous system and immune system at glutamatergic synapses in the PFC across three developmental periods: adolescence, adulthood, and aging. Glutamatergic synapses are tightly juxtaposed with microglia and astrocytes, and each of these cell types exhibits their own developmental trajectory. Not only does chronic stress differentially impact each of these cell types across development, but chronic stress also alters intercellular communication within this quad-partite synapse. These observations suggest that developmental shifts in both neural and immune function across neurons, microglia, and astrocytes mediate shifting effects of chronic stress on glutamatergic transmission.

Keywords: Adolescence; Aging; Astrocytes; Development; Glucocorticoid; Glutamate; Microglia; NF-κB; Sex differences.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Review

MeSH terms

  • Age Factors*
  • Aging* / immunology
  • Aging* / metabolism
  • Animals
  • Chronic Disease*
  • Female
  • Humans
  • Male
  • Prefrontal Cortex* / growth & development
  • Prefrontal Cortex* / immunology
  • Prefrontal Cortex* / metabolism
  • Stress, Psychological* / immunology
  • Stress, Psychological* / metabolism