Neuroimmune and Inflammatory Signals in Complex Disorders of the Central Nervous System

• Published in: Neuroimmunomodulation Vol. 25; no. 5-6; p. 246
• Main Authors: Liberman, Ana Clara, Trias, Emiliano, da Silva Chagas, Luana, Trindade, Pablo, Dos Santos Pereira, Marissol, Refojo, Damian, Hedin-Pereira, Cecilia, Serfaty, Claudio A
• Format: Journal Article
• Language: English
• Published: Switzerland 01.01.2018
• Subjects: Autism; Lesion-induced plasticity; Neurodegeneration; Cytokine; Amyotrophic lateral sclerosis; Depression; Neuroinflammation; Astrocyte; Microglia
• ISSN: 1423-0216
• DOI: 10.1159/000494761

An extensive microglial-astrocyte-monocyte-neuronal cross talk seems to be crucial for normal brain function, development, and recovery. However, under certain conditions neuroinflammatory interactions between brain cells and neuroimmune cells influence disease outcome and brain pathology. Microglial cells express a range of functional states with dynamically pleomorphic profiles from a surveilling status of synaptic transmission to an active player in major events of development such as synaptic elimination, regeneration, and repair. Also, inflammation mediates a series of neurotoxic roles in neuropsychiatric conditions and neurodegenerative diseases. The present review discusses data on the involvement of neuroinflammatory conditions that alter neuroimmune interactions in four different pathologies. In the first section of this review, we discuss the ability of the early developing brain to respond to a focal lesion with a rapid compensatory plasticity of intact axons and the role of microglial activation and proinflammatory cytokines in brain repair. In the second section, we present data of neuroinflammation and neurodegenerative disorders and discuss the role of reactive astrocytes in motor neuron toxicity and the progression of amyotrophic lateral sclerosis. In the third section, we discuss major depressive disorders as the consequence of dysfunctional interactions between neural and immune signals that result in increased peripheral immune responses and increase proinflammatory cytokines. In the last section, we discuss autism spectrum disorders and altered brain circuitries that emerge from abnormal long-term responses of innate inflammatory cytokines and microglial phenotypic dysfunctions.