Neurodevelopmental and Neuropsychiatric Disorders.

Journal: Advances in neurobiology

Volume: 37

Issue: 

Year of Publication: 2024

Affiliated Institutions:  Division of Medical Sciences, University of Victoria, Victoria, BC, Canada. Division of Medical Sciences, University of Victoria, Victoria, BC, Canada. evetremblay@uvic.ca.

Abstract summary 

This chapter will focus on microglial involvement in neurodevelopmental and neuropsychiatric disorders, particularly autism spectrum disorder (ASD), schizophrenia and major depressive disorder (MDD). We will describe the neuroimmune risk factors that contribute to the etiopathology of these disorders across the lifespan, including both in early life and adulthood. Microglia, being the resident immune cells of the central nervous system, could play a key role in triggering and determining the outcome of these disorders. This chapter will review preclinical and clinical findings where microglial morphology and function were examined in the contexts of ASD, schizophrenia and MDD. Clinical evidence points out to altered microglial morphology and reactivity, as well as increased expression of pro-inflammatory cytokines, supporting the idea that microglial abnormalities are involved in these disorders. Indeed, animal models for these disorders found altered microglial morphology and homeostatic functions which resulted in behaviours related to these disorders. Additionally, as microglia have emerged as promising therapeutic targets, we will also address in this chapter therapies involving microglial mechanisms for the treatment of neurodevelopmental and neuropsychiatric disorders.

Authors & Co-authors:  Traetta Marianela Evelyn ME Chaves Filho Adriano Maia AM Akinluyi Elizabeth Toyin ET Tremblay Marie-Ève MÈ

Study Outcome 

Source Link: Visit source

Statistics
Citations :  Abdel-Haq R, Schlachetzki JCM, Glass CK, Mazmanian SK (2019) Microbiome-microglia connections via the gut-brain axis. J Exp Med 216:41–59. https://doi.org/10.1084/jem.20180794
Authors :  4
Identifiers
Doi : 10.1007/978-3-031-55529-9_26
SSN : 2190-5215
Study Population
Male,Female
Mesh Terms
Humans
Other Terms
Autism spectrum disorder;Cytokines;Depression;Microglia;Neuroimmune interactions;Schizophrenia
Study Design
Study Approach
Country of Study
Mali
Publication Country
United States