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Immunoadolescence: Neuroimmune development and adolescent behavior
Institution:1. Northeastern University, Psychology Department, 125 Nightingale Hall, Boston, MA 02115, United States;2. University of Delaware, Department of Psychological and Brain Sciences, 108 Wolf Hall, Newark, DE 19716, United States;1. Department of Psychology, Morehouse College, 830 Westview Dr. SW, Atlanta, GA, 30314, USA;2. Center for Behavioral Neuroscience, Georgia State University, Atlanta, GA, 30302-5090, USA;3. Department of Psychology, College of Arts and Sciences, The University of Tennessee, Knoxville, 312 Ayres Hall, 1403 Circle Drive, Knoxville, TN, 37996-1330, USA,;1. Psychology Department, Northeastern University, 125 Nightingale Hall, Boston, MA 02115, United States;2. Department of Cognitive, Linguistic, and Psychological Sciences, Brown University, 190 Thayer St. Box 1821, Providence, RI 02912, United States
Abstract:The brain is increasingly appreciated to be a constantly rewired organ that yields age-specific behaviors and responses to the environment. Adolescence in particular is a unique period characterized by continued brain maturation, superimposed with transient needs of the organism to traverse a leap from parental dependence to independence. Here we describe how these needs require immune maturation, as well as brain maturation. Our immune system, which protects us from pathogens and regulates inflammation, is in constant communication with our nervous system. Together, neuro-immune signaling regulates our behavioral responses to the environment, making this interaction a likely substrate for adolescent development. We review here the identified as well as understudied components of neuro-immune interactions during adolescence. Synaptic pruning, neurite outgrowth, and neurotransmitter release during adolescence all regulate—and are regulated by—immune signals, which occur via blood-brain barrier dynamics and glial activity. We discuss these processes, as well as how immune signaling during this transitional period of development confers differential effects on behavior and vulnerability to mental illness.
Keywords:Age  Cytokines  Microglia  Rat  Human
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